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Review

Zanthoxylum Species: A Comprehensive Review of Traditional Uses, Phytochemistry, Pharmacological and Nutraceutical Applications

by
Innocent Uzochukwu Okagu
1,
Joseph Chinedu Ndefo
2,*,
Emmanuel Chigozie Aham
1,3 and
Chibuike C. Udenigwe
4,*
1
Department of Biochemistry, University of Nigeria, Nsukka 410001, Enugu State, Nigeria
2
Department of Science Laboratory Technology, University of Nigeria, Nsukka 410001, Enugu State, Nigeria
3
Natural Science Unit, School of General Studies, University of Nigeria, Nsukka 410001, Enugu State, Nigeria
4
School of Nutrition Sciences, University of Ottawa, Ottawa, ON K1H 8M5, Canada
*
Authors to whom correspondence should be addressed.
Molecules 2021, 26(13), 4023; https://doi.org/10.3390/molecules26134023
Submission received: 31 May 2021 / Revised: 22 June 2021 / Accepted: 25 June 2021 / Published: 30 June 2021
(This article belongs to the Special Issue 25th Anniversary of Molecules—Advances in Food Chemistry, Nutraceuticals, Functional Foods, and Dietary Bioactives: Celebrating the Lifetime Achievements of Professor Fereidoon Shahidi)
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Abstract

:
Zanthoxylum species (Syn. Fagara species) of the Rutaceae family are widely used in many countries as food and in trado-medicinal practice due to their wide geographical distribution and medicinal properties. Peer reviewed journal articles and ethnobotanical records that reported the traditional knowledge, phytoconstituents, biological activities and toxicological profiles of Z. species with a focus on metabolic and neuronal health were reviewed. It was observed that many of the plant species are used as food ingredients and in treating inflammation, pain, hypertension and brain diseases. Over 500 compounds have been isolated from Z. species, and the biological activities of both the plant extracts and their phytoconstituents, including their mechanisms of action, are discussed. The phytochemicals responsible for the biological activities of some of the species are yet to be identified. Similarly, biological activities of some isolated compounds remain unknown. Taken together, the Z. species extracts and compounds possess promising biological activities and should be further explored as potential sources of new nutraceuticals and drugs.

1. Introduction

Plants have provided useful sources of nutrients and therapeutic preparations for managing several health conditions in many parts of the world. The vast majority of people who use plant extracts as medicine consider them safer compared to synthetic drugs [1]. In addition, many types of infections, parasitic diseases, and tumors that are resistant to some synthetic drugs have been shown to be treatable using herbal medicines [1,2,3,4,5]. Furthermore, phyto-bioactive compounds have been shown to provide templates that direct the development of some drugs in current use, such as quinine and artemisinins for malaria, and alkaloids and camptothecins for cancer. Zanthoxylum Linn. is a plant genus belonging to Rutaceae, a family that includes over 160 genera and 2000 species with more species still being identified [6]. Plant species in this genus are distributed all over the world with the majority found in Asia, America and Africa [7,8,9,10,11]. Many Z. species are traditionally used as medicinal plants in managing various health conditions. Secondary metabolites isolated from parts of plant species in this genus have demonstrated several pharmacological activities, such as antioxidant, analgesic, anti-inflammatory activities, and modulatory effects against obesity, dementia, and diabetes [12,13,14,15]. Traditionally, decoctions of Z. species, either as a single plant-based preparation or in combination with other plants, are commonly used in treating infection of various kinds, especially those caused by parasites (malaria, leishmaniasis, trypanosomiasis, and other parasitic diseases), sickle cell, tumor, bacterial, fungal, and viral infections [16,17,18,19,20,21]. They are also used to repel insects especially those carrying vector-borne diseases, like mosquitoes, and hence are beneficial in preventing vector-borne diseases [22].
Different aspects of Z. species have been previously reviewed by Negi et al. [23], Singh and Singh [24], Brijwal et al. [25], Mukhtar and Kalsi [26], and Paul et al. [27] for Z. armatum, Supabphol and Tangjitjareonkun [22] for Z. limonella, Zhang et al. [28] for Z. bungeanum, Sinan et al. [29] for Z. gilletii, Guendéhou et al. [30] for Z. zanthoxyloides, and Lu et al. [31] for Z. nitidum. The present review provides comprehensive analysis and discussion covering mostly studies that were not captured in the previous reviews. Specifically, this review summarizes the ethnobotanical reports and biological activities of over 39 Z. species. Specifically, pharmacological potentials of Z. species in relation to metabolic health, such as antioxidant, analgesics, anti-inflammatory, and modulatory effects against markers of organ damages, ulcer, obesity, dementia, and diabetes, were discussed. In addition, isolated secondary metabolites from these species are presented. It is hoped that the outcome of this review will position plant species of this genus as sources of nutraceutical and medicinal compounds while spurring more research on other plants in this genus used in traditional medicine.

2. Traditional Uses of Zanthoxylum Species as Food and Medicine

The traditional uses of Zanthoxylum species as food and in medicinal practices are highlighted in this section. In South Africa and Kenya, pastes made from Z. species are used to suppress pain associated with wounds and to aid wound healing [32,33] while in Nigeria, Z. species like Z. zanthoxyloides are used for treating rheumatism, sickle cell anemia [34,35], toothache, urinary tract infection, and venereal diseases [36]. Similarly, Z. zanthoxyloides root-bark is used in Uganda for healing elephantiasis, toothache, erectile dysfunction, gonorrhea, malaria, dysmenorrhea, and abdominal pain [21,22]. Stem decoction of Z. zanthoxyloides is used in Cote D’Ivoire to relieve tooth pain and to treat infections caused by oral pathogens [37]. In addition, Z. zanthoxyloides leaves are used in Togo to treat wounds, root-bark for toothache, swellings, and worms and to induce lactation post-partum, while the bark is used for relieving pain [38]. In addition, the stem bark decoction is used in treating malaria in Ghana [8]. In Central African Republic, different parts of Z. zanthoxyloides and Z. clava-herculis L. (Syn. Z. macrophyllum Nutt.) are traditionally used for healing diseases of the circulatory and respiratory systems, malaria, diabetes, and hypertension [39].
In Côte D’Ivoire, Z. gilletii is widely used to treat malaria [40], skin infections, and hypertension [41]. In other parts of Africa, decoctions from different parts of Z. gilletii are also used either alone or in combination to treat oral diseases and erectile dysfunction [42], female reproductive issues [43], rheumatism and many kinds of pains [44,45]. According to Kipkore et al. [45], Z. chalybeum bark and seeds are boiled and consumed to relieve pain associated with surgeries and other forms of pain, and to treat malaria and amoebiosis, while burnt ashes from the bark and seeds are used to treat rheumatism. Additionally, stem bark of Z. chalybeum Engl., bark of Z. gilletii and root, fruits, bark, leaves, and stem of Z. usambarense are used alone or in combination in Kenya to treat malaria and related symptoms like fever [46]. Aerial parts and barks of Z. fagara (L.) Sarg. (Syn. Z. affine Kunth and Z. hyemale A. St.-Hil.), Z. elephantiasis Macfad. and Z. martinicense (Lam.) DC.) are traditionally used in Cuba in treating diarrhea, heart diseases, fever, and many types of pain such as ear and muscle, and toothaches [47]. Moreso, aerial parts of Z. acanthopodium DC. are applied traditionally in China as contraceptives, in suppressing pain and in parasite control [48]. In South Africa, roots of Z. capense (Thunb.) Harv. in combination with Callilepis laureola root are taken as oral preparation for respiratory tract and oral infections [49]. Similarly, the Zulu people of South Africa traditionally use bark and root bark decoction of Z. capense for treating tuberculosis [50]. In Thailand, Z. rhetsa (Syn. Z. budrunga) is used as spices and condiments for cooking, as well as for treating infections [1]. In Cameroon and Madagascar, stem bark of Z. gilletii is traditionally applied in treating hypertension and related disorders [51], microbial infection, cancer, and inflammation [3], while the stem bark of Z. tsihanimposa H. Perrier is traditionally used in Madagascar for treating inflammation, skin diseases, microbial infection, and malaria [52].
In general, findings from the articles reviewed show that many Z. species are widely used as food and medicine, in Africa, and different parts of the world for treatment of several diseases. In some cases, different populations use the same plant for different conditions, although the traditional uses of most species in traditional medicine are similar in different parts of the world. The ethnobotanical uses of some Z. species are summarized in Table 1.

3. Phytochemical Constituents of Zanthoxylum Species

The biological activities and toxicity of plants are largely dependent on the composition of their secondary metabolites, also known as phytochemicals. Generally, phytochemicals are non-nutritive compounds synthesized by plants in response to external biotic and abiotic factors. Several classes of phytochemicals have been detected in Zanthoxylum species, such as terpenes, flavonoids, coumarins, phenolic acids, and alkaloids, the most reported among all the classes [99,100,101,102]. In this section, we present only the compounds isolated from different parts of Z. species whose biological activities are related to metabolic and neuronal health. Representative compounds from each of the classes are shown in Figure 1.
In Z. zanthoxyloides, neohesperidin, hesperidin, and quercetin were found to be higher in the root and trunk extracts than in the stem and leaf extracts; hyperoside, quercetin-3-O-glucopyranoside, datiscin, and quercitrin were found to be higher in the leaf extract, while eriocitrin was found in the fruit extract only, and this may explain why the roots have stronger antioxidant properties [103]. Moreover, Tine et al. [104] analyzed volatile compounds in oils from Z. zanthoxyloides and found that the leaf oil is rich in hexadecanoic acid, germacrene D and decanal while pellitorine is the major content of the root and stem bark. Thus, the leaf essential oil is a rich source of antioxidant volatile compounds. Other antioxidant compounds isolated from Z. zanthoxyloides include atanine, hesperetin, isoplatydesmine, N-methylplatydesminium cation, myrtopsine, ribalinine, N-methylatanine, trans-fagaramide, zanthoamides G-I, (+)-sesamin, skimmianine and hesperidin from the fruits [58]; 4′-(4′′-hydroxy-3′′-methylbutyloxy)-2-phenylethanol, hydrocuspidiol, cuspidiol, 4′-(3′′-methylbut-2′′-enyloxy)-3-phenylpropanol, dihydrocusidiol, lupeol, 8-acetonyldihydrochelerythrine, N-isobutyl-(2E,4Z)-deca-2,4-dienamide, (+)-sesamin [62], burkinabins A, B and C, N,N-dimethyllindicarpin, 1,8-di-O-(3-methoxy-4-hydrobenzoyl)-3,6-dihydroxycyclooctane-2,7-endoperoxide, hesperidin, fagaronine, and norchelerythrine [105] from the root bark; and flavonoids (rutin and quercetin) and phenolic acids (caffeic and chlorogenic acids) as the major constituents of the stem bark [106].
The similarity in phytochemical constituents of Z. species is demonstrated by the existence of alkaloids such as 8-acetonyldihydrochelerythrine in Z. paracanthum Kokwaro stem bark [73], Z. zanthoxyloides root bark [105] and Z. gilletii stem bark [107]. Futhermore, terpenoides such as lupeol was also reported in Z. sprucei Engl. stem bark [90] and Z. gilletii stem bark [107,108]. In addition, monoterpenes (myrcene, limonene, and camphene) were reported in essential oils of Z. gilletti leaves, alkaloids (peroxysimulenoline, sanguinarine, xanthoplanine, fagarine I and norchelerythrine) in the bark, root and leaf extracts of Z. zanthoxyloides, Z. bungeanum and Z. gilletii multiple biological activities [44,109]. Also, flavonoides such as quercetin and hesperidin were detected in leaves, fruits and root bark of Z. zanthoxyloides [58,103,105] and in Z. sprucei stem bark (Table 2) [90]. Going further, lignans such as sesamin were reported in Z. nitidum root [56], Z. zanthoxyloides fruits [58] and Z. nitidum stem bark [110]. Based on the above reports, it can be inferred that the existence of similar chemical compounds with multiple biological activities in different parts of Z. species may explain the relatedness in biological activities and the multifunctionality of extracts of these plants in relation to metabolic health [63,66,110].
Based on class of compound and biological activity, phytochemicals present in different parts of Z. species with metabolic health-promoting properties are summarized in Table 2 (alkaloids), Table 3 (flavonoids), Table 4 (coumarins and derivatives), Table 5 (terpenes and derivatives), Table 6 (lignans and derivatives), Table 7 (amides), Table 8 (phytosterols and derivatives, phenol and phenolic acids, tannins, fatty acids, phenylpropanoids and steroids), and Table 9 (other classes of compounds).
Some of the biological properties of chemicals isolated from these plants were discussed in the following sections. Other phytochemical constituents of plants in this genus are discussed in previous reviews [10,95,136,137] and were hence excluded.

4. Health-Related Bioactive Properties of Zanthoxylum Species

Several biological activities have been reported for extracts and isolated compounds from genus Zanthoxylum species mostly in relation to their traditional uses in different parts of the world. The biological activities in relation to neuronal and metabolic health, such as antioxidant, analgesic, chemoprotective, antidiabetic, antiulcer, anti-Alzheimer’s disease, anti-inflammatory, and anti-hypertensive activities are discussed in this section.

4.1. Antioxidant Activities of Zanthoxylum Species

The involvement of oxidative stress in the development and progression of many diseases has been well-characterized. The pathogenesis of neurodegenerative and cardiovascular diseases, many cancers, and malaria involve oxidative stress [138]. Nature has equipped living cells with enzymatic and non-enzymatic antioxidant defense mechanisms to prevent oxidative damage to cellular components [139,140]. However, humans are exposed to large amount of oxidants, warranting additional support with exogenous antioxidants. The role of dietary antioxidants in the prevention and management of many chronic diseases, such as stroke, atherosclerosis, and cancer is increasingly being recognized [141,142,143,144]. Plant-originated compounds may serve as antioxidants to modulate symptoms associated with disease conditions and to improve the quality of life [145]. Many plant-derived compounds have undergone clinical trials for managing chronic diseases and some of their effects are based on antioxidant mechanisms.
Two compounds isolated from Z. bungeanum—magnoflorine from the pericarp and arbutin from the seeds—were shown to have poor antioxidant activities [146]. Considering the traditional use of the fruits as food condiment, Yamazaki et al. [33] isolated hyperoside and quercitrin from Z. bungeanum fruits, which strongly inhibited lipid peroxidation and scavenged free radicals in vitro.
In addition, crude methanol extract of Z. armatum leaves, its solvent fractions and essential oils were reported to demonstrate good radical scavenging, ferric reducing, and divalent metal chelating potentials, which were directly proportional to the total phenolic content of the samples. The authors further showed that ethyl acetate fraction of the extract had higher metal chelating properties while the essential oil has the highest reducing power [85]. Similarly, Negi et al. [123] reported that Z. armatum leave essential oil (containing bornyl acetate, cymene, α-copaene, γ-terpinene, camphene, limonene, linalool, β-ocimene, transcaryophyllene, α-terpinolene and germacrene as the most abundant constituents) exhibited strong 2,2′-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity (IC50 = 27 μg/mL) relative to activity of ascorbic acid (IC50 = 15.0 μg/mL).
Moreover, Imaga et al. [147] showed that Z. zanthoxyloides root extracts had potent antioxidant and anti-sickling effects. This is further supported by Tine et al. [103] who reported that methanol extracts of Z. zanthoxyloides fruits, leaves, stems, trunk barks, and root barks possessed antioxidant properties with leaf and trunk bark extracts showing better activities.
In addition, polyphenol-rich crude ethanol extract of Z. budrunga seeds showed DPPH radical scavenging activity (IC50 = 82.60 μg/mL) compared to ascorbic acid (IC50 = 12.58 μg/mL) [131]. Furthermore, crude ethanol extract of Z. syncarpum Tull. branches and its alkaloidal fraction inhibited DPPH radical scavenging activities with IC50 values of 140 μg/mL and 56 μg/mL, respectively, relative to that by quercetin (IC50 = 4.77 μg/mL); the weak antioxidant activity of the extract is attributed to its low total phenolic content (12.43 mg GAE/g). The crude extract and alkaloidal fraction also potently inhibited hydrochloric acid-induced corrosion, with the alkaloidal fraction being more active than the crude extract. An amino compound, 4-(methylamino)-benzoic acid (Table 9) isolated from the alkaloidal fraction showed the best corrosion inhibitory activity, suggesting that it might be responsible for the corrosion prevention activity of the plant extracts [148].
Similarly, Tatiana et al. [15] compared the antioxidant activities of methanol and aqueous extracts of Z. leprieurii stem bark and found that the methanol extract had higher antioxidant activities, showing that organic solvent was a better solvent for extracting the antioxidant phytochemicals in the plant stem bark. Taken together, these studies demonstrate that Z. species have good antioxidant effects that can be harnessed for prevention and treatment of oxidative stress-related conditions. As shown in Table 2, Table 3, Table 4, Table 5, Table 6, Table 7, Table 8 and Table 9, many antioxidant compounds have been isolated from several Z. species, thus justifying the versatile traditional use of the species in disease management and treatment. Furthermore, future research should explore the antioxidant properties of these compounds in preventing rancidity of oil-based food, and their molecular cellular mechanisms for use as plant-derived nutraceuticals.

4.2. Neuroprotective and Alzheimer’s Disease Modulatory Effects of Zanthoxylum Species

Alzheimer’s disease (AD) and its major symptom, dementia, is prevalent in older people, usually above 70 years old, but also in some younger individuals. This trend is related to the growing number of people with AD risk factors, such as obesity, sustained hyperglycemia, high blood pressure, physical inactivity, and metabolic syndrome [148]. An estimate of more than 120,000 deaths associated with AD was recorded in the US in 2018; this places AD as the fifth leading cause of death in those 65 and above [149]. According to GBD 2016 Alzheimer’s Disease and Other Dementia Collaborators [150], the number of people living with AD increased by 53.9% between 1990 and 2016; it is estimated that this number will double by 2040 [130]. There is a significant socio-economic burden associated with AD, thus the need for a concerted effort to explore new ways of reducing the disease incidence. Considering the involvement of oxidative stress in the pathogenesis of AD, research is needed to fully understand the role and molecular basis antioxidants in preventing and managing the disease and its symptoms. Cholinesterase inhibitors are currently used for the management of AD due to its positive effect in suppressing dementia and other symptoms of the condition. Plant-derived bioactive compounds with cholinesterase inhibitory activities are gaining relevance as potential source of lead compounds for AD.
Wang et al. [126] isolated nine alkylamides, including tetrahydrobungeanool, zanthoamides E and F, ZP-amides A-E and (2E,7E,9E)-N-(2-hydroxy-2-methylpropyl)-6,11-dioxo-2,7,9-dodecatrienamide, from Z. bungeanum pericarps. In vitro neuritogenic test using rat pheochromocytoma PC-12 showed that the nine compounds enhanced neurite outgrowth, indicating that they have neuritogenic activity, without apparent cytotoxicity. Aside zanthoamides E and F and ZP-amide E, other isolated compounds had higher activity than nerve growth factor (NFG) that served as standard. It was also shown that tetrahydrobungeanool (the only isolated compound that has a non-oxygenated unsaturated long fatty acid side chain) exhibited the highest activity suggesting that the side chain may have enhanced its neuritogenic activity. Surprisingly, the compounds showed no activity in the presence of NFG. Although the mechanism behind the loss of activity in the presence of NFG is not known, possible antagonistic interactions between the molecules need to be investigated. Nonetheless, the findings demonstrate that the neurite outgrowth-promoting potentials of the compounds can be harnessed in managing conditions that lead to neurodegeneration, such as AD.
Similarly, the protective effects of Z. capense root methanol and ethyl acetate extracts on rotenone-elicited neuronal injury in SH-SY5Y neuroblastoma cells was investigated in vitro. Pretreatment of the neuroblastoma cells with the extracts was reported to significantly reduce ROS generation while improving intracellular glutathione level comparable to minocycline, a known inhibitor of rotenone activity. However, the extracts further reduced mitochondrial membrane potential compared to rotenone-intoxicated-untreated neuroblastoma cells, suggesting that mitochondrial membrane potential may not be the best indicator of mitochondrial uncoupling because it fluctuates with energy need of cells. In addition, the extracts inhibited rotenone-induced activation of caspase-3 and subsequent apoptosis. Comparatively, methanol extract was reported to have higher neuroprotective effect than ethyl acetate extract [151]. The presence of rutaecarpine and quercetin, previously shown to be anti-apoptotic [119,152] in the methanol extract might be responsible for its neuroprotective potential.
Furthermore, in neuronal PC12 cells injured with hydrogen peroxide, two fractions of methanol extract of Z. bungeanum leaves led to higher viability and reduced injury as characterized by a lower amount of leaked lactate dehydrogenase from damaged neuronal membrane. The fractions contained quercitrin, afzelin and quercetin, and the most active fraction also contained hyperoside [127], but the compounds were not tested individually for the bioactivity. The molecular mechanisms of neuroprotection by the fractions also need to be defined through additional investigation.
Other potential neuro-activity have been reported for extracts and compounds from some Z. species. For example, Plazas et al. [11] screened nine Zanthoxylum species harvested from Colombia for cholinesterase inhibitory activities and Z. schreberi (J.F.Gmel.) Reynel ex C.Nelson (Syn. Z. monophylum (Lam.) P.Wilsom) bark extracts were the most active. Bioassay-directed fractionation led to the isolation of alkaloids such as berberine, chelerythrine and columbamine from Z. schreberi bark (Table 1) that demonstrated strong inhibitory activity against both acetylcholinesterase and butyrylcholinesterase with IC50 values of 0.11, 1.03 and 3.75 µM and 6.40, 3.53, and 2.05 µM, respectively, for berberine, chelerythrine and columbamine. The finding suggests that these compounds should be subjected to in vivo studies to assess their potential for managing AD.
In an in-vitro study, the protective activities of syringic acid, one of the polyphenols isolated in the fruits and barks of Z. heitzii [153] was assessed against ischaemia/reperfusion (OGD/R) neuronal injury. Compared to injured-untreated cells, it was reported that injured neuronal cells pretreated with syringic acid were more viable and released less lactate dehydrogenase, showing that the phenolic acid protected the hippocampal neuronal cells from injury, and oxidative stress, and elevation in intracellular free calcium concentration. In addition, the compound was shown to improve mitochondrial membrane potential, suggesting potent neuroprotective effects [153]. Syringic acid offers neuroprotection by downregulating the expression of phosphorylated (p)-JNK and p-(p38). Collectively, it protects the neurons from injury by boosting antioxidant status while inhibiting oxidation, intracellular calcium release, and apoptosis (via inhibition of both JNK and p38 pathways).

4.3. Antidiabetic Effects of Zanthoxylum Species

Due to the traditional use of Z. species in treating diabetes [154], Kimani et al. [155] assessed their effects in controlling blood sugar level and in treating diabetes. The study showed that aqueous extract of Z. chalybeum stem bark normalized glucose level in oral glucose tolerance test in rats, and in alloxan-induced diabetic rats fed the extract for 14 days. The extract also prevented histological damages in pancreatic β-cells, suggesting that the mechanism of action may be related to stimulation of pancreatic β-cells to secret insulin and increase insulin sensitivity. The extract may have also acted via induction of glycogenesis and glycolysis, and attenuation of oxidative damage to pancreatic β-cells by its antioxidant phytochemicals [156]. Similarly, Agwaya et al. [157] showed that aqueous extract of Z. chalybeum root bark at 400 mg/kg restored blood sugar level of alloxan-induced diabetic rats after 28 days of daily oral administration. The extract also returned the histo-architecture of pancreatic β-cells to near-normal. The ability of the extract to induce regeneration of the pancreatic β-cells and normalize the blood glucose level suggest that it contains phytoconstituents that can induce insulin secretion, inhibit in-vivo glucose synthesis and breakdown of stored glucose, and/or increase the sensitivity of insulin to its receptor and the consequent increase in glucose uptake. Results of these investigations support the traditional use of Z. chalybeum in treating diabetes in Lower Eastern Province of Kenyan [158].
Karki et al. [159] reported that aqueous-alcohol extract of Z. armatum bark suppressed fasting blood glucose levels of streptozotocin-diabetic rats by 43% after oral consumption of 400 mg/kg b.w. for 21 days. The extract further attenuated lipid metabolism dysfunction associated with diabetes and boosted antioxidant status in the liver and kidney. However, the mechanisms of anti-hyperglycemia and anti-hyperlipidemia were not defined. In another study, Rynjah et al. [160] demonstrated that ingestion of aqueous extract of Z. armatum leaves dose-dependently reduced blood glucose level in both normal and alloxan-diabetic mice, suggesting both hypoglycemic and anti-diabetic properties. The extract restored the glucose level of diabetic rat to normal level and strongly suppressed the activities of enzymes that are centrally involved with hyperglycemia, including α-amylase and α/β-glucosidases, in the rats. These results show that phytochemicals in the extracts may have acted via more than one mechanism, including by increasing insulin sensitivity, protecting pancreatic β-cells, regenerating weakened pancreatic β-cells, and inhibition of carbohydrate digestion and assimilation into the blood. For instance, Alam et al. [161] found that methanol extracts of Z. armatum leaves, bark, and fruits inhibited α-glucosidase, a key enzyme involved in carbohydrate digestion in the small intestinal brush border for absorption, by 94%, 97%, and 84%, respectively. The extracts also demonstrated moderate anti-hyperglycemic effects on alloxan-induced diabetes in rats with the leaf extract showing highest glucose suppressing activity. The extracts also prevented hyperlipidemia associated with diabetes, suggesting that the extracts may also be used to attenuate complications associated with diabetes.
Some mechanisms have been proposed for hypoglycemic and pancreatic cell regeneration effects of Z. chalybeum and Z. armatum [155,156,157,159,160,161]. The administration of the extracts to diabetic rats inhibited ATP-dependent K+ channel, leading to reduced intracellular K+ level and concomitant opening of L-type Ca2+ channel leading to increased intracellular Ca2+ level. This causes the depolarization of the pancreatic β-cell membrane and release of insulin. Insulin binds to its receptor on cellular surfaces to induce glucose uptake through glucose transporters (GLUTs), thus lowering blood glucose level. The extracts also inhibit the activities of enzymes involved in glucose production (gluconeogenic enzymes, α-amylase and α/β-glucosidase), thus contributing to reduced blood glucose level. The extracts, by their antioxidant activities, may also prevent reactive oxygen species (ROS)-mediated β-cell damage and apoptosis as well as induce the regeneration of pancreatic β-cells.

4.4. Gastroprotective Effects of Zanthoxylum Species

About 10% of the world population suffer from gastric ulcer [162], a major cause of hospitalization and thousands of deaths globally [163]. Gastric ulcer results from the alteration in the balance between offensive factors, such as gastric acid, ROS and Helicobacter pylori, and protective factors, including mucus secretion, prostaglandins, nitric oxide, bicarbonate ions, enzymatic, and non-enzymatic antioxidants [164,165]. Symptoms of gastric ulcers include burning or constant pain in the stomach [166]. The etiology of gastric ulcer disease is multifactorial including overconsumption of alcohol and non-steroidal anti-inflammatory drugs, stress, smoking, and H. pylori infection [167]. Drugs for gastric ulcer treatment are usually targeted in the control of stomach acid secretion, K+/H+-ATPase pump, H. pylori and resulting inflammation. Conventional anti-cholinergic drugs used in treating gastrointestinal tract disorders, particularly peptic, gastric and duodenal ulcers, exert their effects through stomach acid suppression and self-healing of gastric mucosa lining, but they also elicit side effects such as dry mouth, arrhythmias, erectile dysfunction, constipation, gynaecomastia, urinary retention and dyshematopoiesis [168]. Consequently, there is need for additional and/or alternative drugs that are clinically effective, safe, readily available, and affordable. Many medicinal plants, including some Z. species, are traditionally used in treating ulcers in different parts of the world. The gastroprotective properties of extracts and compounds from some of these plants are discussed below.
In both in vitro and in-vivo models, Boye et al. [169] found that the ethanol extract of Z. zanthxyloides root bark attenuated indomethacin-induced gastric ulceration in rats by 71% and 85% at 250 and 500 mg/kg, respectively compared to 67% by 20 mg/kg esomeprazole, an antiulcer drug. These effects were higher than those reported for a similar dose of Z. nitidum stem bark aqueous extract in aspirin-induced or absolute ethanol-induced ulcer in rats [170]. Moreover, Han et al. [55] documented that aqueous extracts of Z. nitidum roots, stems and leaves strongly suppressed ulcer index of hydrochloric acid and ethanol-provoked ulcerated rats. Differences in activity may be due to the different solvents used in extraction, phytochemical compositions of the extracts, or chemicals used to induce ulcer in the animal models. These factors may also influence the mechanism of gastroprotection of the extracts. For instance, in isolated guinea-pig ileum, the ethanol extract of Z. zanthxyloides root bark inhibited cholinergic receptor activity by 66% compared to 73% by atropine, nicotinic receptor activity by 45% relative to 86% by hexamethonium, and histaminic receptor activity by 60% relative to 66% by mepyramine [169]; atropine, hexamethonium and mepyramine are cholinergic, nicotinic and histaminic receptor antagonists, respectively. This implies that compounds presented in the extract exerted the gastroprotective effect by acting as a muscarinic, histaminic and cholinergic receptor antagonists. Moreover, the Z. nitidum stem bark aqueous extract weakly suppressed stress-generated gastric mucosal lesion by 12% and 45% compared to 80% by ranitidine hydrochloride, a histamine H2 receptor antagonist. Specific compounds in the extracts demonstrating these effects and mechanisms are largely uncharacterized. Nonetheless, total alkaloids from the extracts were proposed to be gastroprotective by increasing nitric oxide, prostaglandin E2 and antioxidant status, and by reducing lipid peroxidation, which support earlier reports that alkaloids may be responsible for the antiulcer activities of Z. nitidum [170,171,172].
The plant part used also influences the extent of bioactivity. For example, Qin et al. [173] reported that extract from Z. nitidum stem was more effective than the root extract in suppressing the amount of gastric acid and free acids in the stomach in iodoacetamide-induced ulcer in rats. Likewise, ethanol extract of Z. rhoifolium stem bark exhibited strong gastroprotective effect in acute gastric lesion models (absolute ethanol, HCl/ethanol and indomethacin-induced gastric lesion in mice, hypothermic-restraint stress, and ischemia/reperfusion in rats) [174]. Observed gastroprotective effects of the extract include protection of the mice mucosal lining, attenuation of ishaemia/reperfusion injury, and modulation of stress-activated gastric lesion/erosion [174]. Moreover, other indirect effects of the extracts have been proposed. Recently, Z. nitidum root water extract was found to dose-dependently inhibit the activity of H. pylori urease, which is responsible for survival of the bacteria, with IC50 value of 1.29 mg/mL, which was lower than the activity of acetohydroxamic acid, a known urease inhibitor (IC50 = 4.56 μg/mL) [56]. Thus, in addition to the gastroprotective mechanisms, Z. nitidum root water extract suppresses the bacterial activity that contribute to gastric mucosal erosion. The urease-inhibiting extract contained magnoflorine, sanguinarine, chelerythrine, skimmianine, and L-sesamin as the major compounds [56], which warrant further investigation for their direct or indirect links to the urease inhibitory and gastroprotective activities.
Some mechanisms have been proposed for the gastroprotective effects of Z. rhoifolium extract [174]. In general, the extract demonstrated strong gastroprotection in a potentially multifactorial mechanism that includes antioxidant protection of the mucosa, activation of KATP channel and increase in nitric oxide availability. Specifically, administration of the extract to a rat model of ulcer activated ATP-dependent K+-channel leading to influx of K+ and increase in intracellular K+ level [174]. This results in hyperpolarization of gastric mucosa membrane causing the release of mucus and bicarbonate ions (HCO3−) to buffer the corrosive effects of gastric acid. Similarly, the extract increased the activity of iNOS likely via IP3K-Akt signaling. iNOS increases the availability of nitric oxide, which activates sGC-cGMP-PKG pathway, resulting in relaxation of smooth muscles and increased blood circulation in the gastric mucosa. Nitric oxide also activates COX-2 which increases prostaglandin-E2 (PG-E2) availability. PG-E2 binds to its receptors (G-Protein-coupled receptor subtypes) to induce mucus and HCO3−secretion while reducing gastric acid secretion. By its radical scavenging activity, the extract also inhibited ROS-mediated damages to mucosal tissues and promoted mucosal tissue regeneration. Collectively, the extract protected the gastric mucosa by increasing mucus and HCO3− secretion while reducing gastric acid release through KATP and IP3K-Akt-iNOS-COX signaling, as well as antioxidant mechanisms.

4.5. Hepatoprotective Effects of Zanthoxylum Species

The liver plays key roles in the biotransformation of many xenobiotics and thus is at risk of damage by toxins. In some cases, the liver converts less toxic compounds to one or more toxic metabolite(s). For survival, the liver is protected by antioxidant system but hepatoxicity may occur at high amounts of toxicants. To investigate the potential hepatoprotective effects, hepatocytes, or animals pre-treated or post-treated with natural products are administered with large doses of hepatotoxins, such as hydrogen peroxide, carbon tetrachloride (CCl4), paracetamol, hypoxanthine/xanthine oxidase, and glucose oxidase.
Hur et al. [175] reported that oral administration of crude methanol extract of Z. bungeanum leaves (250 and 500 mg/kg) and its isolated protocatechuic acid (5, 10 and 20 mg/kg) for 7 days attenuated the elevation in lipid peroxidation and aniline hydroxylase activity in bromobenzene-treated rats. The samples also normalized the activity of epoxide hydrolase isolated from liver homogenate, but showed no significant effect on the activities of aminopyrine-N-demethylase and glutathione S-transferase, which play roles in xenobiotics metabolism. These findings suggest that the crude extract and protocatechuic acid had protective effects on liver by reducing the conversion of bromobenzene to its more hepatotoxic derivative, bromobenzene-3,4-oxide, and increasing the detoxification of bromobenzene-3,4-oxide.
Similarly, Verma and Khosa [176] pretreated rats with defatted ethanolic extract of Z. armatum leaves for 8 days, and, thereafter, treated the rats with CCl4. The extract significantly prevented hepatic necrosis in the pretreated rats compared to the intoxicated and untreated rats. This protection was evidenced by the modulation of parameters of liver status in serum and histological examinations of hepatic tissues of rats that received the extract. In addition, ethyl acetate, chloroform, and methanol extracts of Z. armatum root were evaluated for their ability to prevent paracetamol-mediated hepatic damage in rats and results showed that methanol extract showed the highest hepatoprotective activity, which was related to its high total phenolic content compared to other extracts [177]. Activity-guided fractionation identified lupeol as the active ingredient responsible for the hepatoprotective effects of the methanol extract [177]. The hepatoprotective effects of different parts of Z. armatum could be linked to their strong antioxidant activities [86]. In another study, pre-feeding of rats with aqueous extract of Z. armatum fruit that is rich in ellagic acid, chlorogenic acid, gallic acid, chrysin, quercetin, and epicatechin for 4 days at 100 mg/kg significantly protected the liver cells from toxicity caused by paracetamol overdose [178]. This effect was characterized by significantly lower activities of transaminases in the rat serum. Paracetamol, like many xenobiotics, is first metabolized in the liver, but its metabolites include reactive radicals that attack and damage liver cells. The ability of the Z. armatum fruit extract to protect against liver damage corresponded to the boosting of antioxidant status (elevation in catalase and vitamin C levels in serum and non-protein thiols in liver homogenate) and prevention of lipid peroxidation (lowering of malondialdehyde, a product of lipid peroxidation in the serum) [179]. Taken together, Z. species extracts can be further investigated as hepatoprotective agents, although the active compounds should be isolated and characterized. This will facilitate the elucidation of the molecular mechanisms as well as their pharmacological and nutraceutical applications.

4.6. Lipid-Lowering Effects of Zanthoxylum Species

The link between hyperlipidemia and cardiovascular diseases as well as side effects associated with most currently-available hypolipidemic drugs necessitate the search for compounds with lipid-lowering properties. Wu et al. [180] compared the effects of petroleum ether, ethyl acetate and n-butanol fractions of crude ethanol extract of Z. bungeanum fruit on cholesterol metabolism in liver cell lines (HepG2) and found out that butanol fraction gave the best activity. The authors induced hyperlipidemic condition in the cultured cells using sterols and assessed the suppressive effect of the butanol fraction. It was reported that the butanol fraction (and rutin and hyperin isolated from it) significantly decreased extracellular total cholesterol, free cholesterol, triacylglycerol (TGs) and apoB levels. The treatments also reduced HMGC-R protein level and its mRNA expression in both normal and hyperlipidemic HepG2 cells more than simvastatin, a known HMG-CoA reductase (HMGC-R) inhibitor. Conversely, the fraction increased LDL-R protein level and the expression of genes involved in reverse cholesterol transport (CYP27A1, LXRa and ABCG1) in both normal and hyperlipidemic HepG2 cells. To support the results of cell culture study, the butanol fraction (200 mg/kg/d for 1 month) were shown to significantly reduce total cholesterol and TGs levels more than simvastatin at 3 mg/kg/d in diet-induce obese apoE knock-out mouse. Rutin and hyperin contents of the fraction (Table 3) were proposed to be responsible for the hypolipidemic effects [180].
In addition, ethanol extract of the plant’s pericarp and its eudesmin, β-sitosterol, and sesamin-rich n-butanol fraction [123] as well as flavone-rich ethanol extract of the fruits (Table 6) modulated lipid levels in 3T3-L1 adipocytes and high fat diet-induced obese mice by inhibiting adipocyte differentiation and down-regulating the expression of adipogenic genes and proteins such as fatty acid synthase, sterol regulatory-element binding protein-1 (SREBP-1), peroxisome proliferator-activated regulator-γ (PPAR-γ), and CCAAT/enhancer binding protein-α (CCAAT/EBP-α) [181]. Considering that flavones such as baicalin and naringenin possess obesity-suppressing properties [182,183], the anti-obesity effects of the fruit extract may, in part, be attributed to its flavones content and aliphatic acid amides (β-, γ- and hydroxy-β-sanshool) which inhibited the activity of human acyl-CoA:cholesterol acyltransferase (ACAT) [130]. Similarly, the aqueous extract of Z. heitzii stem also showed anti-hyperlipidemic effect in diet-induced hypercholesterolemic rats [89].
In monosodium glutamate (MSG)-induced hypertension, a study reported that aqueous extract of F. tessmannii stem bark lowered lipid formation and accumulation, and normalized the cardiovascular risk index and cardiac risk ratio that were altered by MSG [130]. Going further, the aqueous extract also attenuated L-NAME-induced hypertension, dyslipidemia and cardiovascular risk by lowering serum levels of triacylglycerol and total cholesterol, and atherogenic index and coronary risk while increasing HDL level and protected kidney, liver and heart tissues from L-NAME-induced organ damages [51].
Taken together, these results proved that Z. bungeanum fruit and pericarp, F. tessmannii stem bark and Z. heitzii stem contain phytochemicals that exhibit hypolipidemic effect in both normal and different models of hyperglycemia by inhibiting fatty acid, cholesterol, and lipoprotein syntheses while increasing reverse cholesterol transport and uptake for breakdown, making them important candidates for the prevention and management of hyperlipidemia, atherosclerosis, hypertension, and lipid-related conditions.

4.7. Antihypertensive Effects of Zanthoxylum Species

Li et al. [184] conducted a study to verify the traditional use of Z. bungeanum leaves in managing hypertension. Exposure of isolated rat aorta, precontracted with phenylephrine (1 µM), with crude methanol extract of Z. bungeanum leaves and its aqueous, n-hexane, ethyl acetate and n-butanol fractions led to relaxation of the aortic rings by 96.8%, 94.6%, 48.6%, 56.5% and 99.5%, respectively. The vasorelaxation effect of the aqueous extract in precontracted rat aortic rings was lost in the absence of vascular endothelium, which implies that the effect was mediated by endothelial signaling. A non-selective NOS inhibitor, L-NAME (10 µM) abolished the vasorelaxation, thus confirming the involvement of nitric oxide. In addition, a selective soluble guanylyl cyclase (sGC) inhibitor (1H-[1,2,4]-oxadiazolo-[4,3-α]-quinoxalin-1-one at 10 µM) significantly inhibited the vasorelaxation of precontracted rat aortic rings induced by the fraction. Thus, the extract may have acted via nitric oxide-mediated activation of sGC to increase cyclic guanosine monophosphate (cGMP) level. One of the ways cGMP mediates vasorelaxation is by activating cGMP-dependent protein kinases which mediate Ca2+ level and subsequent contractility of rat aortic rings. It was also reported that vasorelaxation induced by the most active fraction (butanol fraction) occurred via Ca2+-independent mechanism and store-operated Ca2+ channel (SOCC)-eNOS-sGC-cGMP signaling. Moreover, wortmannin, an inhibitor of protein kinase B (Akt), an upstream signaling molecule of eNOS, partially reduced vasorelaxation effect and totally inhibited elevation in cGMP concentration in the aortic rings by the butanol fraction, indicating additional involvement of the Akt-eNOS-sGC-cGMP signaling.
In another report, Fouda et al. [51] observed that orally administered aqueous extract of Z. gilletii stem barks (100 and 200 mg/kg/d) for 21 days resulted in over 75% reduction in systolic and diastolic blood pressures, pulse pressure, and heart rate in L-NAME-induced hypertension in rats. It was reported that the extract reduced heart rate more than the standard drug, captopril (20 mg/kg/d). The extract also improved antioxidant status, reduced oxidative stress/lipid peroxidation level, cardiac inflammation, and necrosis associated with L-NAME treatment. L-NAME acts by limiting nitric oxide availability, resulting in impaired endothelium-dependent vasodilation and hypertension. The plant extract strongly prevented this process, showing an antihypertensive effect that may be dependent on nitric oxide signaling. Exposure to MSG in early life induces obesity, hypertension, and cardiovascular diseases via induction of endothelial dysfunctions which manifest in later life [185]. The anti-hypertensive effects of Z. gilletii stem bark extract was further demonstrated in its ability to significantly suppress systolic, diastolic blood and pulse pressures in normal and MSG-induced hypertensive mice via NO signaling. The stem bark extract was reported to contain alkaloids, terpenoids, saponins, mucilage, coumarin, flavonoids, gallic tannin, phlobatannin and proanthocyanidols, which have individually shown antihypertensive effects in other studies. The ability of the Z. bungeanum leaves and Z. gilletii stem bark extracts to lower blood pressure and induce vasorelaxation in both in vitro and in vivo models support the use of these species traditionally for hypertension [133], and projects these as potential source of active compounds for hypertension management.

4.8. Cardioprotective Effects of Zanthoxylum Species

The myocardium is susceptible to intense damage during oxidative stress. Sihotang et al. [186] reported that ethyl acetate extract of Z. acanthopodium fruit at 300 mg/kg b.w. protected the myocardium of rats 8 days prior to doxorubicin treatment. The extract caused a reduction in the serum levels of cardiac tissue status markers (troponin T and creatine kinase-MB) and normalized the tissue histo-architecture. The extract was shown to contain alkaloids, flavonoids, tannin, glycosides, and saponin, which have antioxidant properties. Considering that doxorubicin generates free radicals as a mechanism by which it induces cardiomyopathy, the cardioprotection by the extract could be linked with its antioxidant phytochemicals. Earlier, crude aqueous and alcoholic extracts of Z. bungeanum fruits were demonstrated to improve breathing rate in cultured cardiac cells. Hydroxy-α-sanshool, hydroxy-β-sanshool, xanthoxylin, mikanin, hyperin, isoquercitrin, rutin, myricetin, myricitrin, quercitrin, and isovanillic acid isolated from the extracts also increased breathing rates in the cells while kaempferol and luteorin reduced it. In a low Ca2+-level-induced low breathing rate in the cardiac cells, hydroxy-β-sanshool and xanthoxylin improved breathing rate by inducing calcium uptake and modulating sarcoplasmic reticulum Na+/K+- and Ca2+-ATPase activities. Hyperin and quercitrin, however, showed no significant effects on the calcium uptake, and the ATPases activities, suggesting that their mechanism of action is likely Ca2+-independent [125].
Diabetes is a defined risk factor to cardiovascular diseases; sustained hyperglycemia and the associated metabolic dysfunctions exposes the myocardium to oxidation, leading to cardiomyopathy [117,187]. Alloxan, a known hyperglycemic agent induces diabetes by inhibition of glucose-mediated insulin secretion as well as induction of oxidative damage to pancreatic β-cells (insulin-producing cells in islets of Langerhans). These two processes prevent the availability of insulin needed for glucose uptake in the cells; hence, inducing hyperglycemia in diabetes [188]. Agwaya et al. [189] assessed the potential of aqueous extract of Z. chalybeum root bark in modulating diabetes-related myocardial aberrations. The extract at 400 mg/kg/d for 28 days normalized the myocardial histo-architecture. The cardioprotective mechanism has not been defined but might be linked with antioxidant and hypoglycemic phytochemicals in the extract. In addition, the cardioprotective effects of other Z. species should be investigated especially those species with strong antioxidant properties.

4.9. Anti-inflammatory and Analgesic Activities of Zanthoxylum Species

Upon stimulation, cells of the immune system and related organs ignite a cascade of reactions, the inflammatory response, towards elimination of the harmful stimuli. In some cases, the body system is stimulated to ignite immune response against its own cells/organs, a condition that is seen in many auto-immune diseases [190]. Similarly, uncontrolled inflammation causes damage to the host, resulting in diseases collectively known as inflammatory diseases such as inflammatory bowel disease, allergy, asthma, atherosclerosis and many forms of skin irritation [191]. Several drugs classified as steroidal and non-steroidal anti-inflammatory drugs are currently approved for the treatment of some inflammatory conditions [192]. Although many of these drugs are clinically effective, they also elicit side effects such as ulcer, kidney damage, cardiac diseases, and cerebrovascular accident [190,193,194,195,196]. Several mitigation strategies have been suggested, including the combination of anti-inflammatory drugs with other agents that protect cells from damage or the use of safer alternatives.
Medicinal plants with a history of anti-inflammatory activity have been traditionally used to manage inflammation-related conditions. Screening the anti-inflammatory activities of these plants and identifying their active principles might provide new class of anti-inflammatory agents. Several species of Zanthoxylum genus have demonstrated anti-inflammatory properties. In an in vitro study, acetone extract of Z. capense leaves containing moderately high total phenolic and flavonoid contents demonstrated anti-inflammatory property by inhibiting 15-lipoxygenase activity, which converts linoleic acid to leukotrienes, a class of inflammatory mediators. The extract also suppressed nitric oxide synthesis in activated RAW 264.7 macrophage cell lines by 33–86% at 3.12–32 μg/mL and exhibited strong antioxidant activities, and low toxicity against Vero Monkey kidney cell lines with IC50 > 1000 μg/mL [15]. Furthermore, extract of Z. rhetsa stem bark was reported to inhibit inflammation induced by LPS in Raw 264.7 cells by suppression of COX-2 and iNOS as well as the mRNA expression of their upstream transcriptional activator, nuclear factor (NF)-κB [195].
In some studies, the ability of Z. zanthoxyloides root bark to stabilize erythrocyte membrane exposed to hypotonic solution [196], and attenuate inflammation in diabetic rats has been demonstrated [197], showing that the plant root bark has beneficial effects in resolving inflammatory processes associated with diabetes. Ethyl acetate fraction of alcoholic extracts of Z. armatum roots and stems also demonstrated anti-inflammatory effect in different models and blocked the feeling of pains in experimentally-induced pain in mice [197]. Lignans such as eudesmin, horsfieldin, fargesin, kobusin, sesamin, asarinin, planispine A, and pinoresinol-di-3,3-dimethylallyl from root and stem of Z. armatum (Table 6) are reported to be responsible of the activities [198].
Additionally, Chen et al. [124] reported that extracts of Z. nitidum root and stem suppressed physical and histological wounds observed and pains associated with mechanical injury. The extracts significantly reduced the number of writhing in acetic acid-generated writhing test and delayed the duration of pain observation in hot plate test. These results suggest that the extracts have promising analgesic properties. Furthermore, the extracts inhibited acute inflammation generated using carrageenan (paw edema) and chronic inflammation (granuloma) induced by cotton pellets [124].
Several secondary metabolites such as coumarin derivatives (8-formylalloxanthoxyletin, avicennone, (Z)-avicennone, alloxanthoxyletin, avicennol, avicennol methyl ether, cis-avicennol methyl ether, avicennin, xanthoxyletin, luvangetin, scopoletin, and aesculetin dimethyl ether) (Table 4), benzo[c]phenanthridine derivatives (norchelerythrine and arnottianamide), a furoquinoline (γ-fagarine), a triterpene (β-amyrin), and steroids (β-sitosterol and stigmasterol (Table 8)) isolated from Z. avicennae stem bark were subjected to anti-inflammatory activity using fMet-Leu-Phe/cytochalasin B (fMLP/CB)-induced superoxide and elastase release in cultured human neutrophiles. The release of these factors in activated neutrophils has been implicated in the initiation of inflammation. Among the isolated compounds, 8-formylalloxanthoxyletin, alloxanthoxyletin, xanthoxyletin, aesculetin dimethyl ether, and γ-fagarine significantly suppressed superoxide formation (IC50 ≤ 7.65 μg/mL) compared to diphenyleneiodonium standard (IC50 = 0.53 μg/mL). Similarly, 8-formylalloxanthoxyletin, (E)-avicennone, alloxanthoxyletin, avicennin, and xanthoxyletin significantly suppressed elastatase release (IC50 ≤ 8.17 μg/mL) compared to phenylmethylsulfonyl fluoride standard (IC50 = 34.2 μg/mL). Based on these findings, the anti-inflammatory properties of the extract are attributable mostly to its coumarin constituents; thus, these compounds have potential for further exploration as potent anti-inflammatory agents [119].
Wang et al. [199] isolated zanthoamides A–D, bugeanumamide A, (2E,7E,9E)-N-(2-hydroxy-2-methylpropyl)-6,11-dioxo-2,7,9-dodecatrienamide, ZP-amides A-E and tetrahydrobungeanool from Z. bungeanum pericarps. Considering the previously reported anti-inflammatory activities of the plant part and ZP-amides A and D isolated from Z. bungeanum pericarps [199], the compounds were tested against nitric production by LPS-stimulated RAW264.7 macrophages. It was reported that only zanthoamide A, tetrahydrobungeanool, ZP-amides C and D, and (2E,7E,9E)-N-(2-hydroxy-2-methylpropyl)-6,11-dioxo-2,7,9-dodecatrienamide showed inhibitory activities with IC50 values of 48.7, 27.1, 49.8, 112.9 and 39.4 μM, respectively. Some amides from Z. bungeanum pericarps also demonstrated anti-inflammatory activities through the inhibition of nitric oxide synthesis (Table 7).
Based on previously reported anti-inflammatory [119,199] and antioxidant [200] activities, Wang et al. [201] examined the effects of Z. bungeanum seed oil on ovalbumin-induced bronchial asthma, a complex disease whose etiology is related to inflammatory and oxidative processes. In mice with bronchial asthma, orally administered seed oil at 2 g/kg/d of suppressed pulmonary injury and infiltrations of inflammatory cells caused mainly by leukocytes. The seed oil was shown to inhibit the protein levels and mRNA expression of inflammatory cytokines and chemokines and other mediators of inflammation and their receptors as well as signaling of mitogen-activated protein kinases pathway.
Considering its traditional use in relieving bone-related pain [53], Hwang et al. [63] investigated the potential application of Z. bungeanum in treating experimentally-generated osteoarthritis. It was reported that crude extracts of different parts of Z. bungeanum inhibited monosodium iodoacetate-generated inflammation as follows: stalks (65%), roots (11.8%), twigs (84.7%), fruits (72.8%) and leaves (91.6%). The leaves were further extracted with different solvents and the ethanol extract was found to inhibit arthritic inflammation in mice by 91% at 100 mg/kg b.w. The ethanol leave extract also suppressed hind paw edema formation, feeling of pain and histologically-observed tissue damages by inflammatory process more than the standard, celecoxib at 10 mg/kg. In acetic acid-generated writhings, a model of studying the central nervous system (CNS) response to pain, pretreatment of mice with graded doses of extract suppressed the number of abdominal/stomach writhings at 50 and 100 mg/kg similar to the effect of 10 mg/kg of celecoxib. In other models of CNS mediated pain, the extract at 100 mg/kg gave 74% inhibition of hot plate-generated pain and 34% and 56.8% inhibition of phases 1 and 2 of formalin-provoked pain test, respectively [63]. The extract was further reported to downregulate genes that increase feeling of pain (K+-gated regulated membrane protein—KCNJ6) in isolated BV-2 mouse microglia cells, suggesting that the extract inhibited feeling of pain in both peripheral and CNS likely by inhibiting K+-current. In sub-chronic ear edema induced by 12-O-tetradecanoylphorbol-13-acetate (TPA), orally administered extract (25, 50 and 100 mg/kg) increased ear thickness and weight, indicating edema inhibition, and downregulated the protein level and mRNA expression of iNOS and COX-2. Furthermore, the extract suppressed mRNA expression of NF-κB and its ability to activate the expression of iNOS and COX-2 in LPS-activated RAW 264.7 macrophages. When activated, NF-κB induces the translocation of p65 from the cytosol into the nucleus for the activation of iNOS and COX-2 expression. Translocation of p65 from cytosol into the nucleus was reported to be blocked by 100 mg/kg of the extract [63]. The extract also suppressed LPS-activated ROS generation in the macrophages; increase in ROS generation is one mechanism of inducing damages to cells during inflammation. Additionally, the extract was shown to affect two genes whose role in arthritis is not defined; it suppressed hypoxanthine phosphoribosyltransferase-1 gene expression and increased ribosomal protein-L8 gene expression. It is hypothesized that the two genes may be promoting and inhibiting inflammatory events in osteoarthritis, respectively, but further study is required to clarify this effect. Two flavonoids, quercetin and afzelin that have anti-inflammatory and antioxidant activities [121,122], were reported to be isolated from the extract.
In another arthritis model using Freund’s complete adjuvant (FCA)-induced rheumatoid arthritis in rats, Lei et al. [202] topically treated arthritic rats for 21 days with Z. bungeanum-cake-separated moxibustion, a method that is practiced in China. It was reported that the topical treatment significantly suppressed edema formation, histological markers of inflammatory tissue damages and levels of cytokines (IL-1β and TNF-α) in serum. The anti-inflammatory activities of the Z. bungeanum could be attributed to the lignan components that have been shown to suppress inflammation by inhibiting nitric oxide synthesis which can signal the release of inflammatory mediators [203]. Furthermore, Rahman et al. [204] reported that methanol extract of Z. rhetsa stem bark moderately inhibited acetic acid-generated writhings in mice by 47.82% and 58.89% at 250 and 500 mg/kg, respectively compared to 67.30% by reference drug, aspirin at 100 mg/kg. This finding demonstrates that the extract has antinociceptive property. Similarly, at 250 and 500 mg/kg doses, ethanol extract of Z. budrunga root bark was reported to significantly increase the latency time of response to hot plate induced pain (5.80 and 6.81 s) relative to control (3.29 s), but the analgesic activity of the extract was lower than the effect of morphine (9.60 s) [179]. Using another analgesic assay (acetic acid-induced writhings in mice), the authors reported that the extract potently suppressed the number of writhes by 64.58% and 77.43% at 250 and 500 mg/kg, respectively, relative to 81.9% by diclofenac sodium, the reference antinociceptive drug [179]. Taken together, the studies show that Z. species are potential sources of analgesics, anti-arthritis, anti-asthmatic, and generally anti-inflammatory agents.

4.10. Anti-Thrombotic Activity of Zanthoxylum Species

In vitro, several compounds isolated from chloroform fraction of Z. schinifolium bark, including schinicoumarin, acetoxyaurapten, schininallylol, aurapten, collinin, (–)-acetoxycollinin and dictamnine, showed significant antiplatelet aggregatory response with collinin exhibiting the best activity in rabbit platelet aggregation induced by collagen, arachidonic acid and platelet-activating factor [205]. Similarly, among over 30 compounds isolated from Z. schinifolium root bark, 8-methoxyanisocoumarins H, acetoxycollinin, schinilenol, schinindiol, anisocoumarin H, platydesmine, norchelerythrine, amottianamide, tetracosyl ferulate, β-sitosterol, and 7-[(E)-7′-hydroxy-3′,7′-dimethylocta-2′,5′-dienyloxy] coumarin significantly inhibited the platelet aggregation [122]. Moreover, plasminogen activator inhibitor-1 (PAI-1) is a natural negative regulator of urokinase-type plasminogen activator (uPA) and tissue-type plasminogen activator (tPA) that, when over expressed, is implicated in thrombosis, fibrin clogging of organs and arteries. Yu et al. [13] reported the inhibitory effects of Z. nitidum var. tomentosum against PAI-1 in vitro as a potential mechanism of its traditional use in managing blood clotting and circulation disorders in Chinese medicine. This activity guided the isolation of active compound, toddalolactone, which also inhibited clot formation and induced breakdown of ferric chloride-formed clots in vitro. Similarly, toddalolactone inhibited ferric chloride-generated clot formation and pretreatment of mice with toddalolactone (1 mg/kg/d) for 14 days significantly increased bleeding time [14]. Histological assessment of arteries of thrombotic mouse pretreated with toddalolactone showed significant inhibition of thrombus compared to control. Furthermore, toddalolactone at 1 mg/kg/day for 14 days also significantly inhibited hepatic fibrosis induced by oral administration of carbon tetrachloride (150 µL/day for a week) in mice [14]. In addition, histological assessment of liver section of the mice showed strong dose-dependent inhibition of hepatic fibrosis in mice fed toddalolactone. These findings strongly demonstrate that toddalolactone is a potential candidate for preventing and managing thrombosis and other related cardiovascular diseases.

4.11. Antispasmodic Activity of Zanthoxylum Species

Traditionally, different parts of Z. fagara are used in Brazil to suppress muscle spasm and modulate muscle tone and contraction. Crude ethanol extract of the stem bark showed good antispasmodic activity in rat ileum in vitro [124]; however, (–)-R-geilbalansine, hyemaline, O-methylbalsamide, (R)-tembamide, O-methyltembamide, zanthoxyline, nitidine, lupeol, and skimmianine isolated from the extract showed weak activity [124]. The antispasmodic activities of Z. fagara stem bark ethanol extract is relative to that by ethanolic and aqueous extracts of Z. rhoifolium in rabbit duodenum [206]. Additionally, methanol extracts of Z. armatum fruit, bark and leaves that inhibited butyryl cholineesterase also potently relaxed precontracted rabbit jejunum strips, intestine, trachea and thoracic aortic rings, indicating spasmolytic potentials [207]. These reports generally imply that the Z. species are rich sources of lignans that possess muscle-relaxation properties. The biological activities of crude extracts from different parts of Z. species, their solvent fractions and compounds isolated from them have been summarized in Table 10.

5. Toxicological Aspects of Zanthoxylum Species

To ascertain the safety of root bark extract of Z. chalybeum, a common medicinal plant used in treating many diseases in Uganda, Engeu et al. [204] fed Wistar rats with 100 and 4000 mg/kg/day for one month. The researchers reported nephrotoxicity characterized by elevation in creatinine, sodium and potassium levels in serum at 4000 mg/kg. Histological examination of the intestines showed that high doses also induced early signs of intestinal tumor formation. This observation is supported by a recent study which showed that chloroform-methanol extracts of leaves, stem bark, and root bark of Z. chalybeum were lethal to mice at doses above 2000 mg/kg. Similarly, high dose of the crude extract was also cytotoxic to mammalian kidney epithelium cells (Vero199) in vitro. However, the toxicity was substantially diminished upon solvent fractionation, with no sign of toxicity observed for the fractions up to 5000 mg/kg. These observations collectively imply that only low doses are recommended due to safety concerns.
Despite the common traditional uses of Z. gilletii to enhance sexual performance in Peru, South Africa and other regions, the plant extract negatively affected male reproductive system of rats that were fed its ethanol extract for two weeks [204]. Interestingly, a combination of Lepidium meyenii and Z. gilletii improved the fertility depression induced by Z. gilletii in rats [211]. In another study, Ogunbolude et al. [106] reported that 150 µg/mL of ethanol extract of Z. zanthoxyloides stem bark induced genotoxicity and cytotoxicity in human leukocytes. Similarly, extracts of Z. lepreurii and Z. zanthoxyloides at high concentrations were toxic to normal human prostate epithelium cells (PNT2) [58,212]. Methanol extract of Z. zanthoxyloides root bark was also shown to be lethal at high doses by inducing convulsion in mice; the LD50 was recorded to be 5000 mg/kg. Histological examination of mice that died after consuming large doses of the extract showed substantial damage to the liver and kidney [20]. Umaru et al. [213] demonstrated that aqueous extract of Z. zanthoxyloides stem bark dose-dependently reduced bile secretion in rats fed the extracts for 3 weeks. Interestingly, the lipid levels in rats fed the extracts were lower than the control, which implies that the stem bark polar compounds disrupted lipid digestion and absorption, which require the emulsification capacity of the bile. The above findings support the previous report that ingestion of Z. zanthoxyloides at higher doses than the recommended value in Ugandan traditional medicine was characterized by acute stomachache and related gastrointestinal discomfort [214].
In a study to ascertain the maximum tolerable doses of Z. heitzii stem bark from Cameroon, Ntchapda et al. [215] fed wistar rats with scaler doses of aqueous extract (ranging between 3000 and 18,000 mg/kg) once and recorded many signs of toxicity and organ damage especially at high doses. It was reported that the maximum tolerable dose in rodents was 6000 mg/kg b.w. Despite the promising anti-thrombin activity of toddalolactone from Z. nitidum var. tomentosum [13] and other extracts with anti-platelet aggregatory response, caution must be taken to avoid administration of the plant materials or its isolate to people with clotting disorders to avoid worsening the conditions. Generally, it can be inferred from the reviewed studies that only low doses of extract of plants in this genus should be further investigated for therapeutic applications. Additionally, safety doses of all the Z. species of nutritional and medicinal importance should be established to allow consumers make evidence-based decision on the intake doses devoid of toxicity.

6. Conclusions and Future Prospects

There has been heightened efforts to discover natural products as safer alternatives to drugs for managing and treating human diseases. Medicinal plants that are used traditionally for managing health challenges are currently being investigated to validate the folkloric claims. Many compounds isolated from plant origin are showing a wide variety of biological activities. Specifically, over 500 secondary metabolites have been isolated from Z. species and promising biological activities of many of them have been demonstrated. However, the molecular mechanisms of action of most of the bioactive compounds are not known; hence, further studies are warranted to fill this knowledge gap. In addition, the active principles of many extracts of Zanthoxylum species are not yet known. At high doses, some Z. species have exhibited toxicity, inferring that only low doses should be administered in future studies. It is also worth noting that comprehensive toxicity studies on the majority of the plant species, especially in vivo are lacking. Hence, long term safety profile in animal model is required to establish the safety doses. Similarly, bioactive compounds derived from Z. species whose biological activities are only demonstrated in vitro should also be tested in vivo. This is because the physiological barriers may reduce the bioaccessibility and bioavailability of the compounds, thus influencing their amounts and bioactivity in target tissues. Interestingly, the similarity in the phytochemical profiles of the plant species reviewed may explain the relatedness of the species in both their traditional medicinal uses and biological activities. Compounds isolated from Z. species such as hesperidin, sesamin, berberine, rutaceline, nitidine, fagaronine chelerythridine, and sanguinarine among others that demonstrated significant biological activities with known mechanism of action should be subjected to clinical trials to further assess their potential as new drug and nutraceutical candidates or as pharmacophores for the development of new generation of therapeutic agents.

Author Contributions

Conceptualization, I.U.O., J.C.N. and C.C.U.; data curation, E.C.A. and I.U.O.; writing—original draft preparation, J.C.N., E.C.A. and I.U.O.; writing—review and editing, I.U.O. and C.C.U.; funding acquisition, I.U.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research was partially funded by the African German Network of Excellence in Sciences (AGNES), through the program “AGNES Intra-Africa Mobility Grant for Junior Researchers” (I.U.O).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors thank Chioma Patience Ezugwu for providing technical assistance.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

DPPH = 2,2′-diphenyl-1-picrylhydrazyl; IC50 = concentration that can inhibit 50% of the reaction; GAE = gallic acid equivalent; AD = Alzheimer’s disease; NFG = nerve growth factor; ROS = reactive oxygen species; OGD/R = oxygen glucose deprivation/re-oxygenation; JNK = c-Jun N-terminal kinases; p38 MAPK = mitogen activated protein kinase p38; GLUTs = glucose transporters; NO= nitric oxide; HCO3− = bicarbonate; iNOS = inducible nitric oxide synthase; IP3K = inositol-3-phophate kinase; Akt = protein kinase B; SOCC = store-operated Ca2+ channel; eNOS = endothelial nitric oxide synthase; sGC = soluble guanylate cyclase; cGMP = cyclic guanosine monophosphate; PKG = protein kinase G; COX-2 = cyclo-oxygenase type 2; PG-E2 = prostaglandin-E2; KATP = adenosine triphosphate-dependent K+-channel; CCl4 = carbon tetrachloride; TGs = triacylglycerol; HMGC-R = 3-hydroxy-3-methyl glutaryl coenzyme A reductase; MSG= monosodium glutamate; ACAT = acyl-CoA:cholesterol acyltransferase; SREBP-1 = sterol regulatory-element binding protein-1; PPAR-γ = peroxisome proliferator-activated regulator-γ; CCAAT/EBP-α = CCAAT/enhancer binding protein-α; L-NAME = NG-nitro-L-arginine methyl esther; LPS = lipopolysaccharide; mRNA = messenger ribonucleic acid; NF-κB = nuclear factor-κB; fMLP/CB = fMet-Leu-Phe/cytochalasin B; CNS = central nervous system; TPA = 12-O-tetradecanoylphorbol-13-acetate; KCNJ6 = K+-gated regulated membrane protein; FCA = Freund’s complete adjuvant; IL = interleukins; TNF-α = tumor necrotic factor-α; uPA = urokinase-type plasminogen activator and tPA = tissue-type plasminogen activator.

References

  1. Tantapakul, C.; Phakhodee, W.; Ritthiwigrom, T.; Yossathera, K.; Deachathai, S.; Laphookhieo, S. Antibacterial compounds from Zanthoxylum rhetsa. Arch. Pharm. Res. 2012, 35, 1139–1142. [Google Scholar] [CrossRef] [PubMed]
  2. Ochwang’I, D.O.; Kimwele, C.N.; Oduma, J.A.; Gathumbi, P.K.; Mbaria, J.M.; Kiama, S.G. Medicinal plants used in treatment and management of cancer in Kakamega County, Kenya. J. Ethnopharmacol. 2014, 151, 1040–1055. [Google Scholar] [CrossRef] [PubMed]
  3. Tankeo, S.B.; Damen, F.; Awouafack, M.D.; Mpetga, J.; Tane, P.; Eloff, J.N.; Kuete, V. Antibacterial activities of the methanol extracts, fractions and compounds from Fagara tessmannii. J. Ethnopharmacol. 2015, 169, 275–279. [Google Scholar] [CrossRef] [PubMed]
  4. Bunalema, L.; Obakiro, S.; Tabuti, J.R.; Waako, P. Knowledge on plants used traditionally in the treatment of tuberculosis in Uganda. J. Ethnopharmacol. 2014, 15, 999–1004. [Google Scholar] [CrossRef]
  5. Goodman, C.D.; Hoang, A.T.; Diallo, D.; Malterud, K.E.; McFadden, G.I.; Wangensteen, H. Anti-plasmodial effects of Zanthoxylum zanthoxyloides. Planta Med. 2019, 85, 1073–1079. [Google Scholar] [CrossRef]
  6. Groppo, M.; Pirani, J.R. A new species of Zanthoxylum (Rutaceae) with a key to the species from Northeastern Brazil. Phytotaxa 2017, 314, 259–265. [Google Scholar] [CrossRef]
  7. Mabogo, D.E.N. The Ethnobotany of the Vhavenda. Ph.D. Thesis, University of Pretoria, Pretoria, South Africa, 1990. [Google Scholar]
  8. Asase, A.; Oppong-Mensah, G. Traditional antimalarial phytotherapy remedies in herbal markets in southern Ghana. J. Ethnopharmacol. 2009, 126, 492–499. [Google Scholar] [CrossRef]
  9. Massoma, L.; Gasco, M.; Rubio, J.; Yucra, S.; Sock, E.N.; Gonzales, G.F. Effect of the ethanolic extract from Fagara tessmannii on testicular function, sex reproductive organs and hormonal level in adult male rats. J. Androl. 2011, 43, 139–144. [Google Scholar] [CrossRef]
  10. Phuyal, N.; Jha, P.K.; Raturi, P.P.; Rajbhandary, S. Zanthoxylum armatum DC.: Current knowledge, gaps and opportunities in Nepal. J. Ethnopharmacol. 2019, 229, 326–341. [Google Scholar] [CrossRef]
  11. Plazas, E.; Rosana, C.R.; Monica, A.M.; Fernando, B.C.; Cuca, L.E. Metabolomic profiling of Zanthoxylum species: Identification of anticholinesterase alkaloids candidates. Phytochemistry 2019, 168, 112128. [Google Scholar] [CrossRef]
  12. Nurain, I.O.; Bewaji, C.O.; Johnson, J.S.; Davenport, R.D.; Zhang, Y. Potential of three ethnomedicinal plants as antisickling agents. Mol. Pharm. 2017, 14, 172–182. [Google Scholar] [CrossRef]
  13. Yu, B.; Zhang, G.; Jin, L.; Zhang, B.; Yan, D.; Yang, H.; Ye, Z.; Ma, T. Inhibition of PAI-1 activity by toddalolactone as a mechanism for promoting blood circulation and removing stasis by Chinese herb Zanthoxylum nitidum var. tomentosum. Front. Pharm. 2017, 8, 489. [Google Scholar] [CrossRef] [Green Version]
  14. Akakpo-Akue, J.; Kplé, T.K.M.; Coulibaly, K.; Ahon, G.M.; Fofié, Y.; Yapo-Crezoit, A.; Zirihi, G.N.; Kra, A.K.M. Ethnobotanical study of medicinal plants used against sickle cell anaemia in the eastern part of the Côte d’Ivoire. J. Anim. Plant. Sci. 2020, 45, 7839–7852. [Google Scholar] [CrossRef]
  15. Tatiana, K.M.K.; Akakpo-Akue, J.; Yvette, F.; Marcel, A.G.; Julien, G.K.; Mathieu, K.A.K.; Ibrahime, S.; Chiayé, C.A.Y. Sickling cells inhibition and radical scavenging activities of Zanthoxylum leprieurii’s (GUILL) bark extracts: Comparative study. J. Pharm. Res. Int. 2020, 32, 42–50. [Google Scholar] [CrossRef]
  16. Bryant, A.T. Zulu Medicine and Medicine-Men; Struik: Cape Town, South Africa, 1996; pp. 98–105. [Google Scholar]
  17. Rabe, T.; Van Staden, J.V. Antibacterial activity of South African plants used for medicinal purposes. J. Ethnopharmacol. 1997, 56, 81–87. [Google Scholar] [CrossRef]
  18. Van Wyk, B.E.; van Oudtshoorn, B.; Gericke, N. Medicinal Plants of South Africa; Briza Publications: Pretoria, South Africa, 1997; p. 262. [Google Scholar]
  19. Adebayo, S.A.; Dzoyem, J.P.; Shai, L.J.; Eloff, J.N. The anti-inflammatory and antioxidant activity of 25 plant species used traditionally to treat pain in southern African. BMC Complement. Altern. Med. 2015, 15, 159. [Google Scholar] [CrossRef] [Green Version]
  20. Ogwal-Okeng, J.W.; Obua, C.; Anokbonggo, W.W. Acute toxicity effects of the methanolic extract of Fagara zanthoxyloides (Lam.) root-bark. Afr. Health Sci. 2003, 3, 124–126. [Google Scholar]
  21. Andima, M.; Coghi, P.; Yang, L.J.; Wong, V.K.W.; Ngule, C.M.; Heydenreich, M.; Ndakala, A.J.; Yenesew, A.; Derese, S. Antiproliferative activity of secondary metabolites from Zanthoxylum zanthoxyloides Lam: In vitro and in silico studies. Pharm. Commun. 2020, 10, 44–51. [Google Scholar] [CrossRef] [Green Version]
  22. Supabphol, R.; Tangjitjareonkun, J. Chemical constituents and biological activities of Zanthoxylum limonella (Rutaceae): A review. Trop. J. Pharm. Res. 2014, 13, 2119–2130. [Google Scholar] [CrossRef] [Green Version]
  23. Negi, J.S.; Bisht, V.K.; Bhandari, A.K.; Singh, P.; Sundriyal, R.C. Chemical constituents and biological activities of the genus Zanthozylum: A review. Afr. J. Pure Appl. Chem. 2011, 5, 412–416. [Google Scholar]
  24. Singh, T.P.; Singh, O.M. Phytochemical and pharmacological profile of Zanthoxylum armatum DC—An overview. Indian J. Nat. Prod. Res. 2011, 2, 275–285. [Google Scholar]
  25. Brijwal, L.; Pandey, A.; Tamta, S. An overview on phytomedicinal approaches of Zanthoxylum armatum DC: An important magical medicinal plant. J. Med. Plants Res. 2013, 7, 366–370. [Google Scholar] [CrossRef]
  26. Mukhtar, H.M.; Kalsi, V. A review on medicinal properties of Zanthoxylum armatum DC. Res. J. Pharm. Technol. 2018, 11, 2131–2138. [Google Scholar] [CrossRef]
  27. Paul, A.; Kumar, A.; Singh, G.; Choudhary, A. Medicinal, pharmaceutical and pharmacological properties of Zanthoxylum armatum: A review. J. Pharmacogn. Phytochem. 2018, 7, 892–900. [Google Scholar]
  28. Zhang, M.; Wang, J.; Zhu, L.; Li, T.; Jiang, W.; Zhou, J.; Peng, W.; Wu, C. Zanthoxylum bungeanum Maxim. (Rutaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, pharmacokinetics, and toxicology. Int. J. Mol. Sci. 2017, 18, 2172. [Google Scholar] [CrossRef] [PubMed]
  29. Sinan, K.I.; Zengin, G.; Bene, K.; Mahomoodally, M.F. Chemistry and pharmacology of three antiplasmodial traditional medicinal plants from tropical Africa—A review. S. Afr. J. Bot. 2019, 126, 265–276. [Google Scholar] [CrossRef]
  30. Guendéhou, F.; Djossa, B.A.; Kènou, C.; Assogbadjo, C.A.E. Review of studies on Zanthoxylum zanthoxyloids (Lam): Availability and ethnomedical, phytochemical, pharmacological uses. Sch. J. Res. Agric. Biol. 2018, 3, 2456–6527. [Google Scholar]
  31. Lu, Q.; Ma, R.; Yang, Y.; Mo, Z.; Pu, X.; Li, C. Zanthoxylum nitidum (Roxb.) DC: Traditional uses, phytochemistry, pharmacological activities and toxicology. J. Ethnopharmacol. 2020, 260, 112946. [Google Scholar] [CrossRef]
  32. Kigen, G.; Kipkore, W.; Wanjohi, B.; Haruki, B.; Kemboi, J. Medicinal plants used by traditional healers in Sangurur, Elgeyo Marakwet County, Kenya. Pharm. Res. 2017, 9, 333–347. [Google Scholar] [CrossRef]
  33. Bodede, S.O. Phytochemical Investigation and Tissue Culture Studies on the South African Knob Trees, Zanthoxylum capense and Senegalia nigrescens. Ph.D. Thesis, University of KwaZulu-Natal, Westville, South Africa, 2017. [Google Scholar]
  34. Ameh, S.J.; Tarfa, F.D.; Ebeshi, B.U. Traditional herbal management of sickle cell anemia: Lessons from Nigeria. Anemia 2012, 2012, 607436. [Google Scholar] [CrossRef] [Green Version]
  35. Gbadamosi, I.T. An inventory of ethnobotanicals used in the management of sickle cell disease in Oyo State, Nigeria. Bot. Res. Int. 2015, 8, 65–72. [Google Scholar]
  36. Adesina, S.K. The Nigerian Zanthoxylum: Chemical and biological values. Afr. J. Trad. Comp. Alt. Med. 2005, 2, 282–301. [Google Scholar] [CrossRef] [Green Version]
  37. Kiyinlma, C.; Chimène, A.; Allassane, D.; Justin, K.N. Ethnobotanical study and valorization of medicinal plants from the classified forest of Foumbo (Northern Cote D’ivoire). Int. J. Recent Sci. Res. 2020, 11, 38848–38853. [Google Scholar] [CrossRef]
  38. Yaovi, N. Characteristics, fatty acid profile, strategic importance of Zanthoxylum zanthoxyloides (rutaceae) seed oil and sustainable conservation of the species. Int. J. Dev. Res. 2018, 8, 21425–21429. [Google Scholar]
  39. Kosh-Komba, E.; Touckia, I.; Worowounga, X.; Toumnou, A.L.; Mololi, A.; Mukeina, G.; Semballa, S.; Batawilla, K.; Akpagana, K. Case study and phytochemical investigation of Zanthoxylum zanthoxyloids and Zanthoxylum macrophylum (Rutaceae) in the Central African Republic and Togo: A comparative approach. Am. J. PhytoMed. Clin. Ther. 2017, 6, 1. [Google Scholar] [CrossRef]
  40. Zirihi, G.N.; N’guessan, K.; Etien, D.T.; Serikouassi, B.P.H. Evaluation in vitro of antiplasmodial activity of ethanolic extracts of Funtumia elastica, Rauvolfia vomitoria and Zanthoxylum gilletii on Plasmodium falciparum isolates from Côted’Ivoire. J. Anim. Plant. Sci. 2009, 5, 406–413. [Google Scholar]
  41. Zirihi, G.; Yao, D.; Kra-adou, K.; Grellier, P. Phytochemical and pharmacological studies of alcoholic extract of Fagara macrophylla (Oliv) Engl (Rutaceae): Chemical structure of active compound inducing antipaludic activity. J. Chin. Clin. Med. 2007, 2, 205–210. [Google Scholar]
  42. Tarus, P.K.; Coombes, P.H.; Crouch, N.R.; Mulholland, D.A. Benzo[c]phenanthridine alkaloids from stem bark of the Forest Knobwood, Zanthoxylum davyi (Rutaceae). S. Afr. J. Bot. 2006, 72, 555–558. [Google Scholar] [CrossRef] [Green Version]
  43. Sibirina, S.; Djakalia, O.; Mathieu, E.W.; Dossahoua, T. Usages traditionnels de quelques espèces végétales de la forêt marecageuse classée de Port Gauthier, en zone cotière au Sud-ouest de la Côte d’Ivoire. Eur. Sci. J. 2014, 2014, 10. [Google Scholar]
  44. Gaya, C.; Kawaka, J.; Muchugi, A.; Ngeranwa, J. Variation of alkaloids in the Kenyan Zanthoxylum gilletii (De wild Waterman). Afr. J. Plant. Sci. 2013, 7, 438–444. [Google Scholar] [CrossRef]
  45. Kipkore, W.; Wanjohi, B.; Rono, H.; Kigen, G. A study of the medicinal plants used by the Marakwet Community in Kenya. J. EthnoBiol. EthnoMed. 2014, 10, 24. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Omara, T. Antimalarial plants used across Kenyan Communities. Evid.-Based Comp. Alt. Med. 2020, 2020, 4538602. [Google Scholar] [CrossRef] [PubMed]
  47. Die’guez-Hurtado, R.; Garrido-Garrido, G.; Prieto-Gonza´lez, S.; Iznaga, Y.; Gonza´lez, L.; Molina-Torres, J.; Curini, M.; Epifano, F.; Marcotullio, M.C. Antifungal activity of some Cuban Zanthoxylum species. Fitoterapia 2003, 74, 384–386. [Google Scholar] [CrossRef]
  48. Rana, V.S.; Blazquez, M.A. Terpenoid constituents of Zanthoxylum acanthopodium DC. Leaves. J. Essent. Oil Res. 2008, 20, 515–516. [Google Scholar] [CrossRef]
  49. Semenya, S.S.; Maroyi, A. Plants used by Bapedi traditional healers to treat asthma and related symptoms in Limpopo Province, South Africa. Evid.-Based Complementary Altern. Med. 2018, 2018, 2183705. [Google Scholar] [CrossRef]
  50. Cock, I.E.; Van Vuuren, S.F. The traditional use of southern African medicinal plants for the treatment of bacterial respiratory diseases: A review of the ethnobotany and scientific evaluations. J. Ethnopharmacol. 2020, 263, 113204. [Google Scholar] [CrossRef]
  51. Fouda, Y.B.; Tom, E.N.L.; Oumarou, B.A.; Mbolang, L.N.; Kuissu, A.M.T.; Djomeni, P.D.D.; Dimo, T. Aqueous extract of Fagara tessmannii Engl. (Rutaceae) exhibits antihypertensive activity in NO synthase inhibitor-induced hypertensive rats. J. Integr. Cardiol. Open Access 2020, 3, 2–9. [Google Scholar] [CrossRef]
  52. Randrianarivelojosia, M.; Rasidimanana, V.T.; Rabarison, H.; Cheplogoi, P.K.; Ratsimbason, M.; Mulholland, D.A.; Mauclère, P. Plants traditionally prescribed to treat tazo (malaria) in the eastern region of Madagascar. Malar. J. 2003, 2, 25. [Google Scholar] [CrossRef] [Green Version]
  53. Sepsamli, L.; Prihastanti, J.E. Ethnobotany of Balimo (Zanthoxylum nitidum) in the Kanayatn Dayak Community in Tapakng, West Kalimantan. Biosaintifika 2019, 11, 318–324. [Google Scholar] [CrossRef]
  54. Chakthong, S.; Ampaprom, S.; Inparn, S.; Phetkul, U.; Chusri, S.; Limsuwan, S.; Voravuthikunchai, S.P. New alkylamide from the stems of Zanthoxylum nitidum. Nat. Prod. Res. 2019, 33, 153–161. [Google Scholar] [CrossRef]
  55. Han, Z.Z.; Li, R.L.; Yang, T.C.; Zhan, R.T.; Chen, W.W. The effect of Zanthoxylum nitidum on gastric ulcer rats induced by hydrochloric acid and ethanol. J. Guangzhou Univ. Tradit. Chin. Med. 2012, 29, 292–294. [Google Scholar]
  56. Lu, Q.; Li, C.; Wu, G. Insight into the inhibitory effects of Zanthoxylum nitidum against Helicobacter pylori urease and jack bean urease: Kinetics and mechanism. J. Ethnopharmacol. 2020, 249, 112419. [Google Scholar] [CrossRef]
  57. Enechi, O.C.; Amah, C.C.; Okagu, I.U.; Ononiwu, C.; Azidiegwu, V.C.; Ugwuoke, E.O.; Onoh, A.P.; Ndukwe, E.E. Methanol extracts of Fagara zanthoxiloides leaves possesses antimalarial effects and normalizes haematological and biochemical status of Plasmodium berghei-passaged mice. Pharm. Biol. 2019, 57, 577–585. [Google Scholar] [CrossRef] [Green Version]
  58. Tamdem, S.B.G. Phytochemical, Chemopreventive and Antimalarial Activity Evaluation of Five Selected Medicinal Plants from the Cameroonian flora. Ph.D. Thesis, John Moores University, Liverpool, UK, 2019. [Google Scholar]
  59. Burkill, H.M. The Useful Plants of West Tropical Africa; Royal Botanic Gardens: Kew, UK, 1985; pp. 4–6. [Google Scholar]
  60. Ngoumfo, R.M.; Jouda, J.B.; Mouafo, F.T.; Komguem, J.; Mbazoa, C.D.; Shiao, T.C.; Choudhary, M.I.; Laatsch, H.; Legault, J.; Pichette, A.; et al. In vitro cytotoxic activity of isolated acridones alkaloids from Zanthoxylum leprieurii Guill. et Perr. Bioorg. Med. Chem. 2010, 18, 3601–3605. [Google Scholar] [CrossRef]
  61. Ouédraogo, L.; Nacoulma, A.P.; Compaoré, M.; Lagnika, L.; Kiendrebeogo, M. Stem bark of Zanthoxylum zanthoxyloïdes a possible substitute of root bark for the conservation of the species in Burkina Faso. Afr. J. Biotech. 2019, 18, 197–205. [Google Scholar] [CrossRef]
  62. Chaaib, F.; Queiroz, E.F.; Ndjoko, K.; Diallo, D.; Hostettmann, K. Antifungal and antioxidant compounds from the root bark of Fagara zanthoxyloides. Planta Med. 2003, 69, 316–320. [Google Scholar] [CrossRef]
  63. Hwang, K.A.; Kwon, J.E.; Noh, Y.; Park, B.; Jeong, Y.J.; Lee, S.M.; Kim, S.Y.; Kim, I.; Kang, S.C. Effects of Zanthoxylum piperitum ethanol extract on osteoarthritis inflammation and pain. Biomed. Pharm. 2008, 105, 481–490. [Google Scholar] [CrossRef]
  64. Lee, S.; Lim, K. Glycoprotein of Zanthoxylum piperitum DC has a hepatoprotective effect via anti-oxidative character in vivo and in vitro. Toxicol. In Vitro 2008, 22, 376–385. [Google Scholar] [CrossRef]
  65. Kim, M.H.; Lee, H.J.; Park, J.C.; Hong, J.; Yang, W.M. Zanthoxylum piperitum reversed alveolar bone loss of periodontitis via regulation of bone remodeling-related factors. J. Ethnopharmacol. 2017, 195, 137–142. [Google Scholar] [CrossRef]
  66. Hatano, T.; Inada, K.; Ogawa, T.; Ito, H.; Yoshida, T. Aliphatic acid amides of the fruits of Zanthoxylum piperitum. Phytochemistry 2004, 65, 2599–2604. [Google Scholar] [CrossRef]
  67. Cui, H.Z.; Choi, H.R.; Choi, D.H.; Cho, K.W.; Kang, D.G.; Lee, H.S. Aqueous extract of Zanthoxylum schinifolium elicits contractile and secretory responses via β1-adrenoceptor activation in beating rabbit atria. J. Ethnopharmacol. 2009, 126, 300–307. [Google Scholar] [CrossRef]
  68. Burkill, H.M. The Useful Plants of West Tropical Africa, Families M-R, 2nd ed.; The Royal Botanic Garden: Kew, UK, 1998; Volume 4, pp. 1–969. [Google Scholar]
  69. Fonge, B.A.; Egbe, E.A.; Fongod, A.G.N.; Focho, D.A.; Tchetcha, D.J.; Nkembi, L.; Tacham, W.N. Ethnobotany survey and uses of plants in the Lewoh-Lebang communities in the Lebialem highlands, South West Region, Cameroon. J. Med. Plants Res. 2012, 6, 855–865. [Google Scholar]
  70. Sandjo, L.P.; Kuete, V.; Tchangna, R.S.; Efferth, T.; Ngadjui, B.T. Cytotoxic benzophenanthridine and furoquinoline alkaloids from Zanthoxylum buesgenii (Rutaceae). Chem. Cent. J. 2014, 8, 61. [Google Scholar] [CrossRef] [Green Version]
  71. Sagbo, I.J.; Mbeng, W.O. Plants used for cosmetics in the Eastern Cape Province of South Africa: A case study of skin care. Phcog. Rev. 2018, 12, 139–156. [Google Scholar] [CrossRef]
  72. Zhou, X.J.; Chen, X.L.; Li, X.S.; Su, J.; He, J.B.; Wang, Y.H.; Li, Y.; Cheng, Y.X. Two dimeric lignans with an unusual α,β-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production. Bioorg. Med. Chem. Lett. 2011, 21, 373–376. [Google Scholar] [CrossRef]
  73. Kaigongi, M.M.; Lukhoba, C.W.; Yaouba, S.; Makunga, N.P.; Githiomi, J.; Yenesew, A. In vitro antimicrobial and antiproliferative activities of the root bark extract and isolated chemical constituents of Zanthoxylum paracanthum Kokwaro (Rutaceae). Plants 2020, 9, 920. [Google Scholar] [CrossRef]
  74. Charoenying, P.; Teerarak, M.; Laosinwattana, C. An allelopathic substance isolated from Zanthoxylum limonella Alston fruit. Sci. Hort. 2010, 125, 411–416. [Google Scholar] [CrossRef]
  75. Beirigo, P.J.S.; Torquato, H.F.V.; dos Santos, C.H.C.; de Carvalho, M.G.; Castro, R.N.; Paredes-Gamero, E.J.; de Sousa, P.T.; Jacinto, M.J.; da Silva, V.C. [1-8-NαC]-Zanriorb A1, a proapoptotic orbitide from leaves of Zanthoxylum Riedelianum. J. Nat. Prod. 2016, 79, 1454–1458. [Google Scholar] [CrossRef]
  76. Erichsen-Brown, C. Use of Plants for the Past 500 Years; Breezy Creeks Press: Aurora, ON, Canada, 1979. [Google Scholar]
  77. Moerman, D.E. Native American Ethnobotany; Timber Press Inc.: Portland, OR, USA, 1998. [Google Scholar]
  78. Pachón, G.; Rasoanaivo, H.; Azqueta, A.; Rakotozafy, J.C.; Raharisololalao, A.; de Cerain, A.L.; de Lapuente, J.; Borra’s, M.; Moukha, S.; Centelles, J.J.; et al. Anticancer effect of a new benzophenanthridine isolated from Zanthoxylum madagascariense (Rutaceline). In Vivo 2007, 21, 417–422. [Google Scholar]
  79. Halstead, C.W.; Forster, P.I.; Waterman, P.G. Alkaloids from the stem bark of an Australian population of Zanthoxylum ovalifolium. Nat. Prod. Res. 2006, 20, 940–945. [Google Scholar] [CrossRef]
  80. Pavani, P.; Naika, R. Evalution of anti-bacterial activity of zanthoxylum ovalifolium wight (Rutaceae) against selected pathogenic bacteria. Plant. Arch. 2020, 20, 2591–2594. [Google Scholar]
  81. Gonzaga, W.A.; Weber, A.D.; Giacomelli, S.R.; Dalcol, I.I.; Hoelzel, S.C.S.; Morel, A.F. Antibacterial alkaloids from Zanthoxylum Rhoifolium. Planta Med. 2003, 69, 371–374. [Google Scholar] [CrossRef] [PubMed]
  82. Sarkar, F.H.; Yiwei, L. Harnessing the fruits of nature for the development of multi-targeted cancer therapeutics. Cancer Treat. Rev. 2009, 35, 597–607. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Cebrián-Torrejón, G.; Assad-Kahn, S.; Lagarde, N.; Castellano, F.; Leblanc, K.; Rodrigo, J.; Molinier-Frenkel, V.; Rojas de Arias, A.; Ferreira, M.E.; Thirant, C.; et al. Antiproliferative activity of trans-avicennol from Zanthoxylum chiloperone var. angustifolium against human cancer stem cells. J. Nat. Prod. 2012, 75, 257–261. [Google Scholar] [CrossRef]
  84. Choi, H.J.; Song, J.H.; Kwon, D.H.; Baek, S.H.; Ahn, Y.J. Antiviral activity of Zanthoxylum species against influenza virus. Korean J. Med. Crop. Sci. 2008, 16, 273–278. [Google Scholar]
  85. Guleria, S.; Tiku, A.K.; Kurl, A.; Gupta, S.; Sign, G.; Razdan, V.K. Antioxidant and antimicrobial properties of the essential oil and extracts of Zanthoxylum alatum grown in North-Western Himalaya. Sci. World J. 2013, 2013, 790580. [Google Scholar] [CrossRef] [Green Version]
  86. Phuyal, N.; Jha, P.K.; Raturi, P.P.; Rajbhandary, S. Total phenolic, flavonoid contents, and antioxidant activities of fruit, seed, and bark extracts of Zanthoxylum armatum DC. Sci. World J. 2020, 2020, 8780704. [Google Scholar] [CrossRef] [Green Version]
  87. Sandberg, F.; Perera-Ivarsson, P.; El-Seedi, H.R. A Swedish collection of medicinal plants from Cameroon. J. Ethnopharmacol. 2005, 102, 336–343. [Google Scholar] [CrossRef]
  88. Zirihi, G.N.; Mambu, L.; Guédé-Guina, F.; Bodo, B.; Grellier, P. In vitro antiplasmodial activity and citotoxicity of 33 West African plants used for treatment of malaria. J. Ethnopharmacol. 2005, 98, 281–285. [Google Scholar] [CrossRef]
  89. Ntchapda, F.; Maguirgue, K.; Adjia, H.; Etet, P.F.S.; Dimo, T. Hypolipidemic, antioxidant and anti-atherosclerogenic effects of aqueous extract of Zanthoxylum heitzii stem bark in diet-induced hypercholesterolemic rats. Asian Pac. J. Trop. Med. 2015, 2015, 359–365. [Google Scholar] [CrossRef]
  90. Binutu, O.A.; Cordell, G.A. Constituents of Zanthoxylum sprucei. Pharm. Biol. 2000, 38, 210–213. [Google Scholar] [CrossRef]
  91. Chou, S.; Peng, H.; Chang, C.; Yang, J.; Chung, H.; Yang, S.; Wood, W.G.; Chung, J. Zanthoxylum ailanthoides Sieb and Zucc. extract inhibits growth and induces cell death through G2/M-phase arrest and activation of apoptotic signals in Colo 205 human colon adenocarcinoma cells. Anticancer Res. 2011, 31, 1667–1676. [Google Scholar]
  92. Cao, X.L.; Xu, J.; Bai, G.; Zhang, H.; Liu, Y.; Xiang, J.F.; Tang, Y. Isolation of anti-tumor compounds from the stem bark of Zanthoxylum ailanthoides Sieb. & Zucc. by silica gel column and counter-current chromatography. J. Chromatogr. B 2013, 929, 6–10. [Google Scholar] [CrossRef]
  93. Ahsan, M.; Haque, M.R.; Hossain, M.B.; Islam, S.N.; Gray, A.I.; Hasan, C.M. Cytotoxic dimeric quinolone-terpene alkaloids from the root bark of Zanthoxylum rhetsa. Phytochemistry 2014, 103, 8–12. [Google Scholar] [CrossRef]
  94. Adesina, S.K.; Olugbade, T.A.; Akinwusi, D.D.; Bergenthal, D. Extractives from Zanthoxylum lemairei root and stem. Pharmazie 1997, 52, 720–724. [Google Scholar]
  95. Patiño, L.O.J.; Prieto, R.J.A.; Cuca, S.L.E. Zanthoxylum Genus as Potential Source of Bioactive Compounds. In Bioactive Compounds in Phytomedicine; Rasooli, I., Ed.; InTech Open: London, UK, 2012; pp. 185–218. [Google Scholar] [CrossRef] [Green Version]
  96. Costa, R.S.; Lins, M.O.; Le Hyaric, M.; Barros, T.F.; Velozo, E.S. In vitro antibacterial effects of Zanthoxylum tingoassuiba root bark extracts and two of its alkaloids against multiresistant Staphylococcus aureus. Braz. J. Pharmacol. 2017, 27, 195–198. [Google Scholar] [CrossRef]
  97. Ladino, O.J.P.; Suárez, L.E.C. Chemical constituents of the wood from Zanthoxylum quinduense Tul. (Rutaceae). Quim. Nova 2010, 33, 1019–1021. [Google Scholar] [CrossRef] [Green Version]
  98. Xiong, Y.; Huang, G.; Yao, Z.; Zhao, C.; Zhu, X.; Wu, Q.; Zhou, X.; Li, J. Screening effective antifungal substances from the bark and leaves of Zanthoxylum avicennae by the bioactivity-guided isolation method. Molecules 2019, 24, 4207. [Google Scholar] [CrossRef] [Green Version]
  99. Kusuda, M.; Inada, K.; Ogawa, T.; Yoshida, T.; Shiota, S.; Tsuchiya, T.; Hatano, T. Polyphenolic constituent structures of Zanthoxylum piperitum fruit and the antibacterial effects of its polymeric procyanidin on methicillin-resistant Staphylococcus aureus. BioSci. BioTechnol. BioChem. 2006, 70, 1423–1431. [Google Scholar] [CrossRef] [Green Version]
  100. Awouafack, M.D.; Kusari, S.; Lamshöft, M.; Fernandes, C.C.; Vieira, P.C.; Da Silva, V.C.; Dall’Oglio, E.L.; Da Silva, L.E.; De Sousa, P.T. 6-Acetonyl-N-methyl-dihydrodecarine, a new alkaloid from Zanthoxylum riedelianum. J. Braz. Chem. Soc. 2009, 20, 379–382. [Google Scholar]
  101. Mbaze, L.M.; Poumale, H.M.P.; Wansi, J.D.; Lado, J.A.; Khan, S.N.; Iqbal, M.C.; Ngadjui, B.T.; Laatsch, H. α-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae). Phytochemistry 2007, 68, 591–595. [Google Scholar] [CrossRef]
  102. Kosh-Komba, E.; Toumnou, L.A.; Zinga, I.; Touckia, I.; Lembo, P.U.N.Z.W.; Mukeina, G.; Semballa, S.; Yongo, O.D.; Syssa-Magale, J.L. Phytochemical screening, antifungal and antibacterial effect of Zanthoxylum zanthoxyloides and Zanthoxylum macrophylum used in traditional medicine in Yamboro (Central African Republic). Eur. J. Med. Plants 2017, 19, 1–11. [Google Scholar] [CrossRef] [Green Version]
  103. Tine, Y.; Yang, Y.; Renucci, F.; Costa, J.; Wélé, A.; Paolini, J. LC-MS/MS analysis of flavonoid compounds from Zanthoxylum zanthoxyloides extracts and their antioxidant activities. Nat. Prod. Commun. 2017, 12, 1865–1868. [Google Scholar]
  104. Tine, Y.; Diop, A.; Diatta, W.; Desjobert, J.; Boye, C.S.B.; Costa, J.; Wélé, A.; Paolini, J. Chemical diversity and antimicrobial activity of volatile compounds from Zanthoxylum zanthoxyloides Lam. according to compound classes, plant organs and Senegalese sample locations. Chem. Biodivers. 2017, 14, e1600125. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  105. Queiroz, E.F.; Hay, A.; van Diemen, D.; Chaaib, F.; Diallo, D.; Hostettmann, K. New and Bioactive Aromatic Compounds from Zanthoxylum Zanthoxyloides. Planta Med. 2006, 72, e213–e216. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  106. Ogunbolude, Y.; Ibrahim, M.; Elekofehinti, O.O.; Adeniran, A.; Abolaji, A.O.; Rocha, J.B.T.; Kamdem, J.P. Effects of Tapinanthus globiferus and Zanthoxylum zanthoxyloides extracts on human leukocytes in vitro. J. Intercult. EthnoPharm. 2014, 3, 167–172. [Google Scholar] [CrossRef] [PubMed]
  107. Masinde, W.R.G. Phytochemical Investigation of Zanthoxylum gilletii (Rutaceae) for Antiplasmodial Biomolecules. Ph.D. Thesis, University of Nairobi, Nairobi, Kenya, 2014. [Google Scholar]
  108. Djeukeu, K.C.; Kenmogne, K.A.; Azebaze, G.B.A.; Kedi, B.E.P.; Vardamides, J.C.; Sewald, N.; Wansi, D.J. A new aromatic amide from the roots of Zanthoxylum tessmannii (Rutaceae). Chem. Biodivers. 2019, 16, e1800590. [Google Scholar] [CrossRef]
  109. Jirovetzl, L.; Buchbauer, G.; Fleischhacker, W.; Ngassoum, M.B. Analysis of leaf volatiles of Zanthoxylum gilletti used in folk medicine of Cameroon. Planta Med. 1999, 65, 181–183. [Google Scholar] [CrossRef]
  110. Yang, C.H.; Cheng, M.J.; Lee, S.J.; Yang, C.W.; Chang, H.S.; Chen, I.S. Secondary metabolites and cytotoxic activities from the stem bark of Zanthoxylum Nitidum. Chem. Biodiv. 2009, 6, 846–857. [Google Scholar] [CrossRef]
  111. Wangensteen, H.; Ho, G.T.T.; Tadesse, M.; Miles, C.O.; Moussavi, N.; Mikolo, B.; Malterud, K.E. A new benzophenanthridine alkaloid and other bioactive constituents from the stem bark of Zanthoxylum heitzii. Fitoterapia 2016, 109, 196–200. [Google Scholar] [CrossRef]
  112. Ouattara, B.; Jansen, O.; Angenot, L.; Guissou, I.P.; Frederich, M.; Fondu, P.; Tits, M. Antisickling properties of divanilloylquinic acids isolated from Fagara zanthoxyloides Lam. (Rutaceae). Phytomedicine 2009, 16, 125–129. [Google Scholar] [CrossRef]
  113. Wu, J.; Mei, W.L.; Dai, H.F. A new monoterpenoid glycoside from roots of Zanthoxylum simulans. Chin. Tradit. Herb. Drug 2007, 38, 488–490. [Google Scholar]
  114. De Moura, N.F.; Morel, A.F.; Dessoy, E.C.; Zanatta, N.; Burger, M.M.; Ahlert, N.; Porto, G.P.; Baldisserotto, B. Alkaloids, amides and antispasmodic activity of Zantoxylum hyemale. Planda Med. 2002, 68, 534–538. [Google Scholar] [CrossRef]
  115. Fan, M.; Tian, Y.; Chen, G.; Sarker, S.D.; Nahar, L.; Wu, J.; Li, N.; Guo, M. Enrichment and analysis of quaternary alkaloids from Zanthoxylum simulans using weak cation exchange solid-phase extraction coupled with LC–MS. Phytochem. Anal. 2019, 2019, 1–8. [Google Scholar] [CrossRef]
  116. Guo, T.; Dai, L.; Tang, X.; Song, T.; Wang, Y.; Zhao, A.; Cao, Y.; Chang, J. Two new phenolic glycosides from the stem of Zanthoxylum armatum DC. Nat. Prod. Res. 2017, 31, 2335–2340. [Google Scholar] [CrossRef]
  117. Mahgoub, M.A.; Abd-Elfattah, A.S. Diabetes mellitus and cardiac function. Mol. Cell BioChem. 1998, 180, 59–64. [Google Scholar] [CrossRef]
  118. Wu, T.; Zhu, Y. Extracts of Zanthoxylum bungeanum regulate cholesterol accumulation induced by sterols and LPS in vitro and in vivo. J. Chin. Pharm. Sci. 2012, 21, 582–590. [Google Scholar] [CrossRef]
  119. Chen, J.J.; Yang, C.K.; Kuo, Y.H.; Hwang, T.L.; Kuo, W.L.; Lim, Y.P.; Sung, P.J.; Chang, T.S.; Cheng, M.J. New coumarin derivatives and other constituents from the stem bark of Zanthoxylum avicennae: Effects on neutrophil pro-inflammatory responses. Int. J. Mol. Sci. 2015, 16, 9719–9731. [Google Scholar] [CrossRef] [Green Version]
  120. Li, L.; Wu, H.; Liu, S.; Wang, G.; Yan, F.; Feng, J. Chemical constituents from the leaves of Zanthoxylum nitidum (Roxb.) DC. BioChem. Syst. Ecol. 2020, 91, 104080. [Google Scholar] [CrossRef]
  121. Chen, I.S.; Lin, Y.C.; Tsai, I.L.; Teng, C.M.; Ko, F.N.; Ishikawa, T.; Ishii, H. Coumarins and anti-platelet aggregation constituents from Zanthoxylum schinifolium. Phytochemistry 1995, 39, 1091–1097. [Google Scholar] [CrossRef]
  122. Tsai, I.L.; Lin, W.Y.; Teng, C.M.; Ishikawa, T.; Doong, S.L.; Huang, M.W.; Chen, Y.C.; Chen, I.S. Coumarins and antiplatelet constituents from the root bark of Zanthoxylum schinifolium. Planta Med. 2000, 66, 618–623. [Google Scholar] [CrossRef]
  123. Negi, J.S.; Bisht, V.K.; Bhandari, A.K.; Bisht, R.; Negi, S.K. Major constituents, antioxidant and antibacterial activities of Zanthoxylum armatum DC. essential oil. Iran. J. Pharm. Ther. 2012, 11, 68–72. [Google Scholar]
  124. Guo, T.; Deng, Y.; Xie, H.; Yao, C.; Cai, C.; Pan, S.; Wang, Y. Antinociceptive and anti-inflammatory activities of ethylacetate fraction from Zanthoxylum armatum in mice. Fitoterapia 2011, 82, 347–351. [Google Scholar] [CrossRef]
  125. Huang, X.; Kakiuchi, N.; Che, Q.; Huang, S.; Hattori, M.; Namba, T. Effects of extracts of Zanthoxylum fruit and their constituents on spontaneous beating rate of myocardial cell sheets in culture. Phytother. Res. 1993, 7, 41–48. [Google Scholar] [CrossRef]
  126. Wang, Y.; Liao, Z.B.; Cao, R.; Li, H.; Wei, A.Z.; Gao, J.M. Isolation, structural characterization and neurotrophic activity of alkylamides from Zanthoxylum Bungeanum. Nat. Prod. Comm 2017, 12, 1121–1124. [Google Scholar] [CrossRef] [Green Version]
  127. Jeong, C.H.; Kwak, J.H.; Kim, J.H.; Choi, G.N.; Kim, D.O.; Heo, H.J. Neuronal cell protective and antioxidant effects of phenolics obtained from Zanthoxylum piperitum leaf using in vitro model system. Food Chem. 2011, 125, 417–422. [Google Scholar] [CrossRef]
  128. Suematsu, N.; Hosoda, M.; Fujimori, K. Protective effects of quercetin against hydrogen peroxide-induced apoptosis in human neuronal SH-SY5Y cells. NeuroSci. Lett. 2011, 504, 223–227. [Google Scholar] [CrossRef]
  129. Fu, Y.H.; Guo, J.M.; Xie, Y.T.; Hu, J.; Dai, Y.Y.; Zhang, W.; Lin, T.C.; Liu, Y.P. Structural characterization, antiproliferative and anti-inflammatory activities of alkaloids from the roots of Zanthoxylum austrosinense. Bioorganic Chem. 2020, 102, 104101. [Google Scholar] [CrossRef]
  130. Park, Y.D.; Lee, W.S.; An, S.; Jeong, T.S. Human acyl-CoA: Cholesterol acyltransferase inhibitory activities of aliphatic acid amides from Zanthoxylum piperitum DC. Biol. Pharm. Bull. 2007, 30, 205–207. [Google Scholar] [CrossRef] [Green Version]
  131. Islam, K.M.; Biswas, N.N.; Saha, S.; Hossain, H.; Jahan, I.A.; Khan, T.A.; Awang, K.; Shilpi, J.A. Antinociceptive and antioxidant activity of Zanthoxylum budrunga Wall (Rutaceae) seeds. Sci. World J. 2014, 2014, 869537. [Google Scholar] [CrossRef] [Green Version]
  132. Bodede, O.; Moodley, R.; Shaik, S.; Singh, M. Phytochemical analysis with antioxidant and cytotoxicity studies of the bioactive principles from Zanthoxylum capense (small knobwood). Anticancer Agents Med. Chem. 2017, 17, 627–634. [Google Scholar] [CrossRef] [PubMed]
  133. Yamazaki, E.; Inagaki, M.; Kurita, O.; Inoue, T. Antioxidant activity of Japanese pepper (Zanthoxylum piperitum DC.) fruit. Food Chem. 2007, 100, 171–177. [Google Scholar] [CrossRef]
  134. Omosa, L.K.; Mbogo, G.M.; Korir, E.; Omole, R.; Seo, E.J.; Yenesew, A.; Heydenreich, M.; Midiwo, J.O.; Efferth, T. Cytotoxicity of fagaramide derivative and canthin-6-one from Zanthoxylum (Rutaceae) species against multidrug resistant leukemia cells. Nat. Prod. Res. 2021, 35, 579–586. [Google Scholar] [CrossRef] [PubMed]
  135. Júnior, J.M.F.; Silva, M.G.V.; Monteiro, J.A.; Barros, A.S.; Falcão, M.J.C.; de Morais, S.M. Evaluation of antioxidant activity and inhibition of corrosion by Brazilian plant extracts and constituents. Int. J. ElectroChem. Sci. 2016, 11, 3862–3875. [Google Scholar] [CrossRef]
  136. Epifano, F.; Curini, M.; Marcotullio, M.C.; Genovese, S. Searching for novel cancer chemopreventive plants and their products: The genus Zanthoxylum. Curr. Drug Targets 2011, 12, 1895–1902. [Google Scholar] [CrossRef]
  137. Nguyen, X.N.; Pham, M.Q.; Nguyen, T.H.V. Alkaloids and their Pharmacology Effects from Zanthoxylum Genus. In Bioactive Compounds in Nutraceutical and Functional Food for Good Human Health; Sharma, K., Mishra, K., Senapati, K.K., Danciu, C., Eds.; IntechOpen: London, UK, 2020; p. 91685. [Google Scholar] [CrossRef] [Green Version]
  138. Martin, J.B. Molecular basis of the neurodegenerative disorder. N. Eng. J. Med. 1999, 340, 1970–1980. [Google Scholar] [CrossRef]
  139. Djordjevic, V.B. Free radicals in cell biology. Int. Rev. Cytol. 2004, 237, 57–89. [Google Scholar]
  140. Tan, B.L.; Norhaizan, M.E.; Liew, W.P.P.; Sulaiman, R.H. Antioxidant and oxidative stress: A mutual interplay in age-related diseases. Front. Pharm. 2018, 9, 1162. [Google Scholar] [CrossRef] [Green Version]
  141. Willcox, J.K.; Ash, S.L.; Catignani, G.L. Antioxidants and prevention of chronic disease. Crit. Rev. Food Sci. Nutr. 2004, 44, 275–295. [Google Scholar] [CrossRef]
  142. Wilson, D.W.; Nash, P.; Buttar, H.S.; Griffiths, K.; Singh, R.; De Meester, F.; Horiuchi, R.; Takahashi, T. The role of food antioxidants, benefits of functional foods, and influence of feeding habits on the health of the older person: An overview. Antioxidants 2017, 6, 81. [Google Scholar] [CrossRef] [Green Version]
  143. Huang, D. Dietary antioxidants and health promotion. Antioxidants 2018, 7, 9. [Google Scholar] [CrossRef] [Green Version]
  144. Goñi, I.; Hernández-Galiot, A. Intake of nutrient and non-nutrient dietary antioxidants. Contribution of macromolecular antioxidant polyphenols in an elderly Mediterranean population. Nutrients 2019, 11, 2165. [Google Scholar] [CrossRef] [Green Version]
  145. Kumar, V.; Khan, A.A.; Tripathi, A.; Dixit, P.K.; Bajaj, U.K. Role of oxidative stress in various diseases: Relevance of dietary antioxidants. J. Phytopharm. 2015, 4, 126–132. [Google Scholar]
  146. Hisatomi, E.; Matsui, M.; Kobayashi, A.; Kubota, K. Antioxidative activity in the pericarp and seed of Japanese pepper (Zanthoxylum piperitum DC). J. Agric. Food Chem. 2000, 48, 4924–4928. [Google Scholar] [CrossRef]
  147. Imaga, N.O.A.; Shaire, E.A.; Ogbeide, S.; Samuel, K.A. In vitro biochemical investigations of the effects of Carica papaya and Fagara zanthoxyloides on antioxidant status and sickle erythrocytes. Afr. J. BioChem. Res. 2011, 5, 226–236. [Google Scholar]
  148. Rizzi, L.; Rosset, I.; Roriz-Cruz, M. Global epidemiology of dementia: Alzheimer’s and vascular types. BioMed Res. Int. 2014, 2014, 908915. [Google Scholar] [CrossRef]
  149. Alzheimer’s Association Report (AAR). 2020 Alzheimer’s disease facts and figures. Alzheimer’s Dement. 2020, 16, 391–460. [Google Scholar] [CrossRef]
  150. GBD 2016 Alzheimer’s disease and other dementia Collaborators (2019). Global, regional, and national burden of Alzheimer’s disease and other dementias, 1990–2016, A systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2019, 18, 88–106. [CrossRef] [Green Version]
  151. Seoposengwe, K.; van Tonder, J.J.; Steenkamp, V. In vitro neuroprotective potential of four medicinal plants against rotenone-induced toxicity in SH-SY5Y neuroblastoma cells. BMC Complementary Altern. Med. 2013, 13, 353. [Google Scholar] [CrossRef] [Green Version]
  152. Bao, M.H.; Dai, W.; YJ, L.; Hu, C.P. Rutaecarpine prevents hypoxia-reoxygenation-induced myocardial cell apoptosis via inhibition of NADPH oxidases. Can. J. Physiol. Pharm. 2011, 89, 177–186. [Google Scholar] [CrossRef]
  153. Cao, Y.; Zhang, L.; Sun, S.; Yi, Z.; Jiang, X.; Jia, D. Neuroprotective effects of syringic acid against OGD/R-induced injury in cultured hippocampal neuronal cells. Int. J. Mol. Med. 2016, 38, 567–573. [Google Scholar] [CrossRef] [Green Version]
  154. Arun, K.; Paridhavi, M. An ethnobotanical, phytochemical and pharmacological utilization of widely distributed species Zanthoxylum: A comprehensive overview. Int. J. Pharm. Invent 2012, 2, 24–35. [Google Scholar]
  155. Kimani, C.N.; Mbaria, J.M.; Suleiman, M.; Gakuya, D.; Kiama, S.G. Antihyperglycemic activity of Zanthoxylum chalybeum stem bark extract in diabetic rats. J. Phytopathol. 2015, 4, 183–189. [Google Scholar]
  156. Jarald, E.; Joshi, S.B.; Jain, D.C. Diabetes and herbal medicines. Iran. J. Pharm. Ther. 2008, 7, 97–106. [Google Scholar]
  157. Agwaya, M.S.; Vuzi, P.C.; Nandutu, A.M. Hypoglycemic activity of aqueous root bark extract Zanthoxylum chalybeum in alloxan-induced diabetic rats. J. Diabetes Res. 2016, 2016, 8727590. [Google Scholar] [CrossRef] [Green Version]
  158. Keter, L.K.; Mutiso, P.C. Ethnobotanical studies of medicinal plants used by traditional health practitioners in the management of diabetes in Lower Eastern Province, Kenya. J. Ethnopharmacol. 2012, 139, 74–80. [Google Scholar] [CrossRef]
  159. Karki, H.; Upadhayay, K.; Pal, H.; Singh, R. Antidiabetic potential of Zanthoxylum armatum bark extract on streptozotocin-induced diabetic rats. Int. J. Green Pharm. 2014, 8, 77–83. [Google Scholar] [CrossRef]
  160. Rynjah, C.V.; Devi, N.N.; Khongthaw, N.; Syiem, D.; Majaw, S. Evaluation of the antidiabetic property of aqueous leaves extract of Zanthoxylum armatum DC. using in vivo and in vitro approaches. J. Trad. Complement. Med. 2018, 8, 134–140. [Google Scholar] [CrossRef]
  161. Alam, F.; Saqib, Q.S.U.; Ashraf, M. Zanthoxylum armatum DC extracts from fruit, bark and leaf induce hypolipidemic and hypoglycemic effects in mice- in vivo and in vitro study. BMC Complement. Altern. Med. 2018, 18, 68. [Google Scholar] [CrossRef] [Green Version]
  162. Gomaa, M.S.; Abd El-Mottaleb, N.A.; Aamer, H.A. Antioxidant and anti-inflammatory activities of alpha lipoic acid protect against indomethacin-induced gastric ulcer in rats. BioMed Pharmacother. 2018, 101, 188–194. [Google Scholar] [CrossRef] [PubMed]
  163. Abubakar, I.; Tillmann, T.; Banerjee, A. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013, A systematic analysis for the Global burden of disease study 2013. Lancet 2015, 385, 117–171. [Google Scholar] [CrossRef]
  164. Byrge, N.; Barton, R.G.; Enniss, T.M.; Nirula, R. Laparoscopic versus open repair of perforated gastroduodenal ulcer: A National surgical quality improvement program analysis. Am. J. Surg. 2013, 206, 957–963. [Google Scholar] [CrossRef] [PubMed]
  165. Ayantunde, A.A. Current opinions in bleeding peptic ulcer disease. J. Gastrointestin Dig. Syst. 2014, 4, 172–180. [Google Scholar] [CrossRef] [Green Version]
  166. Palle, S.; Kanakalatha, A.; Kavitha, C.N. Gastroprotective and antiulcer effects of Celastrus paniculatus seed oil against several gastric ulcer models in rats. J. Diet. Suppl. 2017, 15, 373–385. [Google Scholar] [CrossRef]
  167. Rao, C.V.; Ojha, S.K.; Radhakrishnan, K.; Govindarajan, R.; Rastogi, S.; Mehrotra, S.; Pushpangadan, P. Antiulcer activity of Utleria salicifolia rhizome extract. J. Ethnopharmacol. 2004, 91, 243–249. [Google Scholar] [CrossRef]
  168. Henry, D.A.; Langman, M.J.S. Adverse effects of antiulcer drugs. Drugs 1981, 21, 444–459. [Google Scholar] [CrossRef]
  169. Boye, A.; Koffuor, G.A.; Boampong, J.N.; Amoateng, P.; Ameyaw, E.O.; Ansah, E.O.; Addai, G.M.; Adjei, C.K.; Addo, J.; Penu, D.K.A. Gastroprotective effect and safety assessment of Zanthoxylum Zanthoxyloides (Lam) Waterm root bark extract. Am. J. Pharm. Toxicol. 2012, 7, 73–80. [Google Scholar]
  170. Bhattacharya, S.; Zaman, K. Ameliorative effect of Zanthoxylum nitidum root in chemical and stress induced gastric mucosal lesions in rats. Middle-East. J. Sci. Res. 2012, 12, 1349–1353. [Google Scholar] [CrossRef]
  171. Pang, H.; He, H.; Jian, L.J.; Gao, Z.R.; Wei, Q.; Jia, X.D. Study on the effect of the total alkaloids of Zanthoxylum nitidum on gastric ulcer. Pharm. Clin. Chin. Mater. Med. 2007, 23, 38–39. [Google Scholar]
  172. Pang, H.; He, H.; Jia, X.D.; Jian, L.J.; Wei, Q.; Gao, Z.R. Effect of the total alkaloids from Zanthoxylum nitidum on gastric mucosal defensive factors in rats with gastric ulcer. Lishizhen Med. Mater. Med. Res. 2007, 18, 533–534. [Google Scholar]
  173. Qin, Z.H.; Chen, W.X.; Li, R.L.; Han, Z.Z.; Yang, T.C.; Zhan, R.T.; Chen, W.W. Comparative study on effects of anti-gastritis, gastric mucosal protection and gastrointestinal movement promotion of root and stem of Zanthoxylum nitidum. J. Chin. Med. Mat. 2016, 39, 164–169. [Google Scholar]
  174. Freitas, F.F.B.P.; Fernandes, H.B.; Piauilino, C.A.; Pereira, S.S.; Carvalho, K.I.M.; Chaves, M.H.; Soares, P.M.G.; Miura, L.M.C.V.; Leite, J.R.S.A.; Oliveira, R.C.M.; et al. Gastroprotective activity of Zanthoxylum rhoifolium Lam. in animal models. J. Ethnopharmacol. 2011, 137, 700–708. [Google Scholar] [CrossRef] [Green Version]
  175. Hur, J.M.; Park, J.G.; Yang, K.H.; Park, J.C.; Park, J.R.; Chun, S.S.; Choi, J.S.; Choi, J.W. Effect of methanol extract of Zanthoxylum piperitum leaves and of its compound, protocatechuic acid, on hepatic drug metabolizing enzymes and lipid peroxidation in rats. BioSci. BioTechnol. BioChem. 2003, 67, 945–950. [Google Scholar] [CrossRef] [Green Version]
  176. Verma, N.; Khosa, R.L. Hepatoprotective activity of leaves of Zanthoxylum armatum DC in CCl4-induced hepatotoxicity in rats. Indian J. BioChem. Biophys. 2010, 47, 124–127. [Google Scholar]
  177. Talluri, M.R.; Gummadi, V.P.; Battu, G.R.; Killari, K.N. Evaluation of hepatoprotective activity of Zanthoxylum armatum on paracetamol-induced liver toxicity in rats. Indian J. Pharm. Sci. 2019, 81, 138–145. [Google Scholar] [CrossRef]
  178. Sabir, S.M.; Rocha, J.B.T.; Boligon, A.A.; Athayde, M.L. Hepatoprotective activity and phenolic profile of Zanthoxylum alatum Roxb. fruit extract. Pak. J. Pharm. Sci. 2017, 30, 1551–1556. [Google Scholar]
  179. Islam, M.K.; Acharzo, A.K.; Saha, S.; Hossain, H.; Shilpi, J.A.; Das, A.K.; Biswas, N.N. Bioactivity studies on Zanthoxylum budrunga Wall (Rutaceae) root bark. Clin. Phytosci. 2018, 4, 24. [Google Scholar] [CrossRef] [Green Version]
  180. Wu, T.; Zhong, L.; Hong, Z.; Li, Y.; Liu, X.; Pan, L.; Xin, H.; Zhu, Y. The effects of Zanthoxylum bungeanum extract on lipid metabolism induced by sterols. J. Pharm. Sci. 2015, 127, 251–259. [Google Scholar] [CrossRef] [Green Version]
  181. Gwon, S.Y.; Ahn, J.Y.; Kim, T.W.; Ha, T.Y. Zanthoxylum piperitum DC ethanol extract suppresses fat accumulation in adipocytes and high fat diet-induced obese mice by regulating adipogenesis. J. Nutr. Sci. Vitam. 2012, 58, 393–401. [Google Scholar] [CrossRef] [Green Version]
  182. Lee, H.; Kang, R.; Hahn, Y.; Yang, Y.; Kim, S.S.; Cho, S.H.; Chung, S.I.; Yoon, Y. Antiobesity effect of baicalin involves the modulatons of proadipogenic and antiadipogenic regulators of the adipogensis pathway. Phytother. Res. 2009, 23, 1615–1623. [Google Scholar] [CrossRef]
  183. Mulvihill, E.E.; Assini, J.M.; Sutherland, B.G.; DiMattia, A.S.; Khami, M.; Koppes, J.B.; Swyez, C.G.; Whitman, S.C.; Huff, M.W. Naringenin decreases progression of atherosclerosis by improving dyslipidemia in high-fat-fed low-density lipoprotein receptor-null mice. Arteioscler. Thromb. Vasc. Biol. 2010, 30, 742–748. [Google Scholar] [CrossRef] [Green Version]
  184. Miranda, R.A.; da Silva Franco, C.C.; de Oliveira, J.C.; Barella, L.F.; Tófolo, L.P.; Ribeiro, T.A.; Pavanello, A.; da Conceição, E.P.S.; Torrezan, R.; Armitage, J.; et al. Cross-fostering reduces obesity induced by early exposure to monosodium glutamate in male rats. Endocrine 2017, 55, 101–112. [Google Scholar] [CrossRef]
  185. Li, X.; Kim, H.Y.; Cui, H.Z.; Cho, K.W.; Kang, D.G.; Lee, H.S. Water extract of Zanthoxylum piperitum induces vascular relaxation via endothelium-dependent NO-cGMP signaling. J. Ethnopharmacol. 2010, 129, 197–202. [Google Scholar] [CrossRef]
  186. Fouda, Y.B.; Tom, E.N.L.; Atsamo, A.D.; Bonabe, C.; Dimo, T. Effects of stem bark aqueous extract of Fagara tessmannii Engl (Rutaceae) on cardiovascular risks related to monosodium glutamate-induced obesity in rat: In vivo and in vitro assessments. J. Ethnopharamacol. 2020, 260, 112972. [Google Scholar] [CrossRef]
  187. Sihotang, Y.; Silalahi, J.; Anjelisa, P. Cardioprotective effect of ethylacetate extract of Zanthoxylum acanthopodium Dc. against doxorubicin-induced cardiotoxicity in rats. Int. J. PharmTech. Res. 2016, 9, 249–253. [Google Scholar]
  188. Dhalla, N.S.; Pierce, G.N.; Innes, I.R.; Beamish, R.E. Pathogenesis of cardiac dysfunction in diabetes mellitus. Can. J. Cardiol. 1985, 1, 263–281. [Google Scholar]
  189. Lenzen, S. The mechanisms of alloxan and streptozotocin-induced diabetes. Diabetologia 2008, 51, 216–226. [Google Scholar] [CrossRef] [Green Version]
  190. Agwaya, M.S.; Nandutu, A.M.; Vuzi, P.C. Protective effects of Zanthoxylum chalybeum in diabetes-induced myocardial dysfunction in rats. Eur. J. Med. Plants 2016, 12, 1–10. [Google Scholar] [CrossRef]
  191. Chen, L.; Deng, H.; Cui, H.; Fang, J.; Zuo, Z.; Deng, J.; Li, Y.; Wang, X.; Zhao, L. Inflammatory responses and inflammation-associated diseases in organs. Oncotarget 2018, 9, 7204–7218. [Google Scholar] [CrossRef] [Green Version]
  192. Modi, C.M.; Mody, S.K.; Patel, H.B.; Dudhatra, G.B.; Kumar, A.; Avale, M. Toxicopathological overview of analgesic and anti-inflammatory drugs in animals. J. Appl. Pharm. Sci. 2012, 2, 149–157. [Google Scholar]
  193. Harirforoosh, S.; Asghar, W.; Jamali, F. Adverse effects of nonsteroidal antinflammatory drugs: An update of gastrointestinal, cardiovascular and renal complications. J. Pharm. Pharm. Sci. 2013, 16, 821–847. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  194. Gabriel, S.E.; Jaakkimainen, L.; Bombardier, C. Risk for serious gastrointestinal complications related to use of non-steroidal anti-inflammatory drugs. A meta-analysis. Ann. Intern. Med. 1991, 328, 1313–1316. [Google Scholar]
  195. Salmon, S.D. Cyclooxygenase-2 inhibitors and cardiovascular risk. Curr. Opin. Cardiol. 2006, 21, 613–617. [Google Scholar] [CrossRef]
  196. Thu, N.B.; Trung, T.N.; Ha, D.T. Zanthoxylum rhetsa stem bark extract inhibits LPS-induced COX-2 and iNOS expression in RAW264.7 cells via the NF-κB inactivation. Nat. Prod. Sci. 2010, 16, 265–270. [Google Scholar]
  197. Oyedapo, O.O.; Famurewa, A.J. Antiprotease and membrane stabilizing activities of extracts of Fagara zanthoxyloides, Olax subscorpioides and Tetrapleura tetraptera. Int. J. Pharm. 1995, 33, 65–69. [Google Scholar] [CrossRef]
  198. Aloke, C.; Nwachukwu, N.; Ugwuja, E.I.; Idenyi, J.N.; Nwachi, E.U.; Obasi, I.O.; Oga, O. Effects of Zanthoxylum zanthoxyloides leaves on blood glucose, lipid profile and some liver enzymes in alloxan induced diabetic rats. Int. J. Sci. Nat. 2012, 3, 497–501. [Google Scholar]
  199. Ha, S.Y.; Youn, H.; Song, C.S.; Kang, S.C.; Bae, J.J.; Kim, H.T.; Lee, K.M.; Eom, T.H.; Kim, I.S.; Kwak, J.H. Antiviral effect of flavonol glycosides isolated from the leaf of Zanthoxylum piperitum on influenza virus. J. MicroBiol. 2014, 52, 340–344. [Google Scholar] [CrossRef]
  200. Wang, Y.; Li, C.H.; Luo, B.; Sun, Y.N.; Kim, Y.H.; Wei, A.Z.; Gao, J.M. Isobutylhydroxyamides from Zanthoxylum bungeanum and their suppression of NO production. Molecules 2016, 21, 1416. [Google Scholar] [CrossRef] [Green Version]
  201. Yang, S.Y.; Tai, B.H.; Song, S.B.; Li, W.; Yan, X.T.; Sun, Y.N.; Thao, N.P.; Kim, Y.H. NF-κB activation and PPAR transactivational effects of a new aliphatic acid amide from pericarps of Zanthoxylum piperitum. Bull. Korean Chem. Soc. 2014, 35, 2361–2366. [Google Scholar] [CrossRef] [Green Version]
  202. Wang, J.Q.; Li, X.W.; Liu, M.; Wang, S.C.; Cao, Z.F. Inhibitory effect of Zanthoxylum bungeanum seed oil on ovalbumin-induced lung inflammation in a murine model of asthma. Mol. Med. Rep. 2016, 13, 4289–4302. [Google Scholar] [CrossRef] [Green Version]
  203. Lei, X.; Cheng, S.; Peng, H.; He, Q.; Zhu, H.; Xu, M.; Wang, Q.; Liu, L.; Zhang, C.; Zhou, Q.; et al. Anti-inflammatory effect of Zanthoxylum bungeanum-cake-separated moxibustion on rheumatoid arthritis rats. Afr. J. Tradit. Complement. Altern. Med. 2016, 13, 45–52. [Google Scholar] [CrossRef] [Green Version]
  204. Rahman, M.T.; Alimuzzaman, M.; Ahmad, S.; Chowdhury, A.A. Antinociceptive and antidiarrhoeal activity of Zanthoxylum rhetsa. Fitoterapia 2002, 73, 340–342. [Google Scholar] [CrossRef]
  205. Engeu, P.E.; Tumusiime, R.; Agwaya, M.; Mugisha, G.; Grace, N.; Galiwango, B.; Paul, W. Repeat-dose effects of Zanthoxylum chalybeum root bark extract: A traditional medicinal plant used for various diseases in Uganda. Afr. J. Pharm. Pharmacol. 2008, 2, 101–105. [Google Scholar]
  206. Chen, W.X.; Qin, Z.H.; Zeng, D.; Han, Z.Z.; Zhan, R.T.; Tan, Y.; Chen, W.W. Comparative study on effects of anti-contusion injury, analgesia and antiinflammation of root and stem of Zanthoxylum nitidum. Zhong Yao Cai 2015, 38, 2358–2363. [Google Scholar]
  207. Barros, G.S.G.; Matos, F.J.A.; Vieira, J.E.V.; Souza, M.P.; Medeiros, M.C.J. Pharmacological screening of some Brazillian plants. Pharm. Pharmac. 1970, 22, 116–118. [Google Scholar] [CrossRef]
  208. Alam, F.; Shah, A.J. Butyrlycholine esterase inhibitory activity and effects of extracts (fruit, bark and leaf) from Zanthoxylum armatum DC in gut, airways and vascular smooth muscles. BMC Complement. Altern. Med. 2019, 19, 180. [Google Scholar] [CrossRef]
  209. Shi, X.; Pan, X.; Li, Y.; Ma, W.; Wang, H.; Xu, C.; Li, L. Xanthoplanine attenuates macrophage polarization towards M1 and inflammation response via disruption of CrkL-STAT5 complex. Arch. BioChem. Biophys. 2020, 683, 108325. [Google Scholar] [CrossRef]
  210. Xia, L.; You, J.; Li, G.; Sun, Z.; Suo, Y. Compositional and antioxidant activity analysis of Zanthoxylum bungeanum seed oil obtained by supercritical CO2 fluid extraction. J. Am. Oil Chem. Soc. 2011, 88, 23–32. [Google Scholar] [CrossRef]
  211. Kim, M.H.; Lee, H.; Ha, I.J.; Yang, W.M. Zanthoxylum piperitum alleviates the bone loss in osteoporosis via inhibition of RANKL-induced c-fos/NFATc1/NF-κB pathway. Phytomedicine 2021, 80, 153397. [Google Scholar] [CrossRef]
  212. Lembè, D.M.; Gasco, M.; Gonzales, G.F. Synergistic effect of the hydroalcoholic extract from Lepidium meyenii (Brassicaceae) and Fagara tessmannii (Rutaceae) on male sexual organs and hormone level in rats. Pharm. Res. 2013, 6, 80–86. [Google Scholar] [CrossRef] [Green Version]
  213. Umaru, H.A.; Clarkson, W.P.; Christopher, K. Effect of stem bark extract of Fagara zanthoxyloides on bile secretion in rats. Am. J. Res. Commun. 2019, 7, 1–9. [Google Scholar]
  214. Anokbonggo, W.W.; Odoi-Adome, R.; Oluju, P.M. Traditional methods in management of diarrhoeal diseases in Uganda. Bull. WHO 1990, 68, 359–363. [Google Scholar]
  215. Ntchapda, F.; Maguirgue, K.; Kemeta, A.D.R.; Jean, M.; Djedouboum, A.; Dimo, T. Acute toxicity studies of the stem bark extract of Zanthoxylum heitzii A. & P. (Rutaceae) on haematological parameters, and body temperature. Int. J. Pharma Res. Health Sci. 2015, 3, 630–642. [Google Scholar]
Molecules 26 04023 g001 550
Figure 1. Representative compounds from the different classes of phytochemicals isolated from Zanthoxylum species.
Figure 1. Representative compounds from the different classes of phytochemicals isolated from Zanthoxylum species.
Molecules 26 04023 g001
Table
Table 1. Ethnobotanical applications of Zanthoxylum species around the world.
Table 1. Ethnobotanical applications of Zanthoxylum species around the world.
Plant SpeciesPart UsedRegion or CountryTraditional UsesRefs.
Z. nitidum (Roxb.) DC.S, RKanayatn Dayak Community, West Kalimantan, IndonesiaBoiled with water or chewed raw to prevent alcohol intoxication and heal respiratory diseases[53]
SThailandFor treating toothache and oral pathogens[54]
R, S, LChina and PortugalFor treating ulcer[55,56]
Z. zanthoxyloides Waterman (Syn. Fagara zanthoxyloides Lam.RB, S, SB, LNigeriaFor treating rheumatism, sickle cell anemia, toothache, malaria, urinary tract infection and venereal diseases[34,35,36,57]
RBUgandaFor treating elephantiasis, toothache, sexual impotence, gonorrhea, malaria, dysmenorrhea and abdominal pain[20,21]
SCote D’ IvoirePrepared as a decoction to relieve tooth pains and to treat infection by oral pathogens[37]
LTogoFor treating wounds[38]
RBFor treating toothache, swellings, and worms and induce lactation post-partum
S, SBFor relieving pains
SBGhanaPrepared as a decoction for treating malaria[8]
DPYamboro Community of Central African RepublicFor healing diseases of circulatory and respiratory systems, malaria, diabetes, and hypertension[39]
FCameroonFor managing fever, malaria, tumors and sickle cell anemia[58]
SB, R, LTo suppress pains, and treat arthritis, leprosy, stomachache and venereal diseases[59,60]
S, RBurkina FasoFor treating sickle cell[61]
Z. gilletii (De Wild) P.G. Waterman (Syn. Z. marcrophylla or F. gilletii)RB, SB, LCôte d’IvoireRoot bark, stem bark and leaves are used for treating malaria
stem bark is used for treating fungal infection		[40]
BKenyaFor treating malaria, rheumatism, cough, urinary tract infection and many kinds of pains[44,46]
SBCameroon and MadagascarFor treating microbial infection, cancer, inflammation, hypertension and related disorders[3,51]
Z. clava-herculis L. (Syn. Z. macrophyllum Nutt.)SB, LCameroonFor treating microbial infection, diabetes, and hypertension[39]
Z. davyi Waterm.L, S, R, SBZulu, South Africa
Vhavenda, South Africa		Leaves and stem are powdered and used to dress wounds from snakebite and decoction from these parts are used in for treating severe coughs and colds
Spines for treating infected wounds, leaves for chest pains, stem bark to treat boils, pleurisy and toothache while for mouth ulcers, sore throats and as an aphrodisiac		[42]
Z. bungeanum Maxim. (Syn. Z. piperitum Benn.)L, SChinaFor treating infection and bone diseases[62,63,64,65]
L, F, BJapanFor treating bacterial and fungal infections[66]
Z. schinifolium Siebold & Zucc.L, R, SEastern AsiaFor healing stomach pains, diarrhea, jaundice, all kinds of pain and cold[67]
Z. buesgenii (Engl.) P.G. WatermanL, R, SSierra LeoneFor treating inflammatory conditions like arthritis and rheumatism as well as venereal diseases[68]
South-Western CameroonTo increase libido and improve fertility in males[69,70]
Z. capense HarvL, R
R
B, RB		South Africa
Limpopo province
Zulu people		For treating abdominal pain, wounds, infections, asthma
The roots are powdered with C. laureola root and taken as oral preparation for respiratory tract and oral infection
Prepared as a decoction for treating tuberculosis		[16,17,18,19,71]
[49]
[50]
Z. usambarense (Engl.)
Kokwaro		R, F, B, S, LKenyaFor treating malaria[46]
Z. tessmannii EnglSBCameroon;
Madagascar		For boosting libido and treating tumor, gonorrhea and other infections, swellings, erectile dysfunction, hypertension and heart diseases[9,51,72]
Z. chalybeum Engl.SBKenyaFor treating malaria[46]
Z. paracanthum KokwaroSBKenyaFor treating tumor and abdominal infection[73]
Z. lepreurii Guill. & Perr.,SBCôte D’Ivoire; NigeriaFor treating malaria and sickle cell[14,15,35]
Z. limonella (Dennst.) Alston.EOMexico; ThailandIn suppressing muscle spasm and as natural herbicide[74,75]
Z. fagara (L.) Sarg. (Syn. Z. affine Kunth and Z. hyemale A. St.-Hil.)AP, BCubaFor treating diarrhea, cardiac disorders, fever and many types of pains such as ear and muscle pain and toothaches[47]
Z. elephantiasis Macfad.APCubaFor treating diarrhea, cardiac disorders, fever and many types of pains such as ear and muscle pain and toothaches[47]
Z. martinicense (Lam.) DC.APCubaFor treating diarrhea, cardiac disorders, fever and many types of pains such as ear and muscle pain and toothaches[47]
Z. riedelianum Engl.LBrazilFor treating tumors and suppressing toothache and pains[75]
Z. acanthopodium DC.APChinaAs contraceptives and in suppressing pains and in parasite control[48]
Z. rhetsa DC. (Syn. Z. budrunga DC.)APThailandFor treating infections[1]
Z. americanum Mill.DPUSA; CanadaFor treating tumors and fungal infections of skin, and respiratory, urinary, genital and gastrointestinal tract[76,77]
Z. madagascariense BakerSBMadagascarFor treating cancer and tuberculosis[78]
Z. ovalifolium (Engl.) FinkelsteinSBAustraliaFor treating cancer[79]
FIndiabacterial and fungal infections[80]
Z. rhoifolium Lam.SBBrazil; FranceMicrobial infection of the mouth, malaria, skin and wounds[81]
Z. tsihanimposa H. PerrierSBMadagascarTreating inflammation, skin diseases, microbial infection and malaria[52]
Z. schreberi (J.F.Gmel.) Reynel ex C.Nelson (Syn. Z. monophylum (Lam.) P.Wilsom)R, BColombiaMemory loss and related conditions[11]
Z. caribaeum Lam. (Syn. Z. chiloperone var. angustifolium Engl.)SBFrance; PortugalFor treating cancer and swellings[82,83]
Z. armatum DC. (Syn. Z. alatum Roxb. and Z. planispinum Siebold & Zucc.)F, B, L, RAbbottabad; NepalTreating oral pathogens, cough, diabetes, tumor, microbial infections[84,85,86]
Z. heitzii (Aubrev. & Pellegr.) P.G. WatermanSBCameroonTreating urogenital infections, malaria, cancer, cardiopathies, and hypertension and weight management[87,88,89]
Z. sprucei Engl.SBPeruTreating tumor[90]
Z. parachanthum KokwaroSBKenyaFor treating tumors[2]
Z. ailanthoides Seibold. & Zucc.SB, SChinaFor treating tumors and HIV[91,92,93]
Z. lemairei (De Wild) P.G. WatermanSBNigeriaFor healing malaria and running stomach[94]
Z. tingoassuiba A. St.-Hil.BBrazilMicrobial infections, inflammation, stomach ache, muscle pains and as analgesic[95,96]
Z. quinduense Tul.SBColombiaFor treating fungal infection of humans and plants[97]
Z. avicennae (Lam.) DC.B, LChina; KoreaFor treating fungal infection of humans and plants[98]
Z. coreanum NakaiLKoreaFor treating oral pathogens and cough[84]
SB = stem bar, L = leaves, S = seeds, RB = RB, AP = Aerial part, R = whole root, F = fruits EO = essential oil; DP = all parts/different parts.
Table
Table 2. Alkaloidal compounds isolated from Zanthoxylum species with their biological activities.
Table 2. Alkaloidal compounds isolated from Zanthoxylum species with their biological activities.
Isolated CompoundBiological ActivitiesPart of PlantRefs.
Zanthoxylum alkaloids with anti-obesity activities
6-HydroxypellitorineAnti-obesity activityZ. heitzii stem bark [111]
HeitziquinoneAnti-obesity activityZ. heitzii stem bark [111]
IsoarnottianamideAnti-obesity activityZ. heitzii stem bark [111]
Rhoifoline BAnti-obesity activityZ. heitzii stem bark [111]
SylvamideAnti-obesity activityZ. heitzii stem bark [111]
Zanthoxylum alkaloids with antioxidant, gastroprotective and anti-inflammatory activities
N,N-dimethyllindicarpinAntioxidant activityZ. zanthoxyloides root bark[105]
1,8-di-O-(3-methoxy-4-hydrobenzoyl)-3,6-dihydroxycyclooctane-2,7-endoperoxideAntioxidant activityZ. zanthoxyloides root bark[105]
FagaronineAntioxidant activityZ. zanthoxyloides root bark[105]
NorchelerythrineAntioxidant activityZ. zanthoxyloides root bark[105]
Trans-fagaronine Antioxidant activityZ. zanthoxyloides root bark[105]
8-AcetonyldihydrochelerythrineAntioxidant activityF. zanthoxyloides root bark and Z. paracanthum stem bark [62,73]
Myrtopsineantioxidant activityZ. zanthoxyloides fruits[58]
RibalinineAntioxidant activityZ. zanthoxyloides fruits[58]
N-isobutyl-(2E,4Z)-octa-2,4-dienamide, N-isobutyl-(2E,4Z)-deca-2,4-dienamideAntioxidant activityF. zanthoxyloides root bark [62]
Burkinabin AAntioxidant activityF. zanthoxyloides root [112]
Burkinabin BAntioxidant activityF. zanthoxyloides root [112]
Burkinabin CAntioxidant activityF. zanthoxyloides root [112]
SanguinarineGastroprotective activity Z. gilletii bark, root and leaves and Z. nitidum root [56,113]
Fagarine IAnti-inflammatory activityZ. gilletii bark, root and leaves [44]
Zanthoxylum alkaloids with multiple biological activities
PeroxysimulenolineAnti-inflammatory and anti-platelet aggregation activitiesZ. gilletii bark, root and leaves and Z. austrosinense root [44,113]
SkimmianineAntioxidant and chemopreventive activitiesZ. zanthoxyloides fruits[58]
XanthoplanineAnti-inflammatory and analgesic activitiesZ. bungeanum roots[63,65]
Zanthoxylum alkaloids with antispasmodic and anti-thrombotic activities
(-)-R-GeilbalansineAntispasmodic activity Z. fagara stem bark [114]
HyemalineAntispasmodic activity Z. fagara stem bark [114]
O-MethylbalsamideAntispasmodic activity Z. fagara stem bark [114]
ZanthoxylineAntispasmodic activity Z. fagara stem bark [114]
PalmatineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ChelerythrineAnti-thrombotic activity Different parts of Z. bungeanum[115]
8--O--DemethylchelerythrineAnti-thrombotic activity Different parts of Z. bungeanum[115]
N--MethylcanadineAnti-thrombotic activity Different parts of Z. bungeanum[115]
N-MethyltetrahydrocolumbamineAnti-thrombotic activity Different parts of Z. bungeanum[115]
10--Demethyl--magnoflorineAnti-thrombotic activity Different parts of Z. bungeanum[115]
3--GlucosideAnti-thrombotic activity Different parts of Z. bungeanum[115]
MagnocurarineAnti-thrombotic activity Different parts of Z. bungeanum[115]
IsotembetarineAnti-thrombotic activity Different parts of Z. bungeanum[115]
8--Methoxy--isotembetatrineAnti-thrombotic activity Different parts of Z. bungeanum[115]
MagnoflorineAnti-thrombotic activity Different parts of Z. bungeanum[115]
SimulenolineAnti-thrombotic activity Different parts of Z. bungeanum[115]
BenzosimulineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ZanthodiolineAnti-thrombotic activity Different parts of Z. bungeanum[115]
(–)-N-AcetylanonanineAnti-thrombotic activity Different parts of Z. bungeanum[115]
(–)-N-AcetylnornuciferineAnti-thrombotic activity Different parts of Z. bungeanum[115]
N-AcetyldehydroanonaineAnti-thrombotic activity Different parts of Z. bungeanum[115]
Benzo [C] phenanthridineAnti-thrombotic activity Different parts of Z. bungeanum[115]
DecarineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ArnottianamideAnti-thrombotic activity Different parts of Z. bungeanum[115]
7-FagarineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ZanthosimulineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ZanthobugeanineAnti-thrombotic activity Different parts of Z. bungeanum[115]
HuajiaosimulineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ZanthobisquinoloneAnti-thrombotic activity Different parts of Z. bungeanum[115]
EdulitineAnti-thrombotic activity Different parts of Z. bungeanum[115]
ArborininAnti-thrombotic activity Different parts of Z. bungeanum[115]
Aesculetin dimethyl etherAnti-thrombotic activity Different parts of Z. bungeanum[115]
OxynitidineAnti-thrombotic activity Z. nitidum stem bark[116]
OxyavicineAnti-thrombotic activity Z. nitidum stem bark[116]
OxychelerythrineAnti-thrombotic activity Z. nitidum stem bark[116]
DihydrochelerythrineAnti-thrombotic activity Z. nitidum stem bark[116]
6-AcetonyldihydrochelerythrineAnti-thrombotic activity Z. nitidum stem bark[116]
ArnottianamideAnti-thrombotic activity Z. nitidum stem bark[116]
LiriodenineAnti-thrombotic activity Z. nitidum stem bark[116]
N-Acetyldehydroanonaine Anti-thrombotic activity Z. nitidum stem bark[116]
N-AcetylanonaineAnti-thrombotic activity Z. nitidum stem bark[116]
Epizanthocadinanine AAnti-thrombotic activity Z. nitidum stem bark[116]
Zanthoxylum alkaloids with no reported biological activity
BocconolineNot specifiedZ. davyi stem bark [42]
6-HydroxydihydrochelerythrineNot specifiedZ. davyi stem bark [42]
6-Methoxy-7-demethyldihydrochelerythrine Not specifiedZ. davyi stem bark [42]
Table
Table 3. Flavonoids and their derivatives isolated from Zanthoxylum species with anti-inflammatory, antioxidant, hypolipidemic, antispasmodic and cardioprotective activities.
Table 3. Flavonoids and their derivatives isolated from Zanthoxylum species with anti-inflammatory, antioxidant, hypolipidemic, antispasmodic and cardioprotective activities.
Isolated CompoundBiological ActivitiesPart of PlantRefs.
QuercitrinAnti-inflammatory activityZ. zanthoxyloides leaves [103]
AfzelinAnti-inflammatory and antioxidant activities Z. bungeanum leaves [112,117]
Datiscin Antioxidant activityZ. zanthoxyloides root and leave[103]
NeohesperidinAntioxidant activityZ. zanthoxyloides root and stem[103]
Eriocitrin Antioxidant activityZ. zanthoxyloides fruits[103]
HyperosideAntioxidant activityZ. zanthoxyloides root and stem[103]
HesperidinAntioxidant activityZ. zanthoxyloides root and stem[103]
HesperetinAntioxidant activityZ. zanthoxyloides fruits[58]
HyperinHypolipidemic activityZ. bungeanum fruit [112]
DiosmetinAntispasmodic activity Z. nitidum leaves[118]
VitexinAntispasmodic activity Z. nitidum leaves[118]
IsoquercitrinCardioprotective activityZ. bungeanum fruits [112]
MyricetinCardioprotective activityZ. bungeanum fruits [112]
MyricitrinCardioprotective activityZ. bungeanum fruits [112]
RutinHypolipidemic, antioxidant and anti-inflammatory activities Z. bungeanum fruit [112]
Quercetin Antioxidant and chemoprotective activitiesZ. zanthoxyloides leaves [103]
Quercetin-3-O-glucopyranosideAntioxidant and chemoprotective activitiesZ. zanthoxyloides leaves [103]
Table
Table 4. Coumarins and their derivatives isolated from Zanthoxylum species with anti-inflammatory, antioxidant, antispasmodic and anti-thrombotic activities.
Table 4. Coumarins and their derivatives isolated from Zanthoxylum species with anti-inflammatory, antioxidant, antispasmodic and anti-thrombotic activities.
Isolated CompoundBiological ActivitiesPart of the PlantRefs.
8-FormylalloxanthoxyletinAnti-inflammatory activityZ. avicennae stem bark [119]
(Z)-avicennoneAnti-inflammatory activityZ. avicennae stem bark [119]
AlloxanthoxyletinAnti-inflammatory activityZ. avicennae stem bark [119]
AvicennolAnti-inflammatory activityZ. avicennae stem bark [119]
Avicennol methyl etherAnti-inflammatory activityZ. avicennae stem bark [119]
cis-avicennol methyl etherAnti-inflammatory activityZ. avicennae stem bark [119]
AvicenninAnti-inflammatory activityZ. avicennae stem bark [119]
XanthoxyletinAnti-inflammatory activityZ. avicennae stem bark [119]
LuvangetinAnti-inflammatory activityZ. avicennae stem bark [119]
ScopoletinAnti-inflammatory activityZ. avicennae stem bark [119]
Aesculetin dimethyl etherAnti-inflammatory activityZ. avicennae stem bark [119]
7,8,9-trimethoxycoumarinAntioxidant activityZ. gilletii root[108]
7,8-dimethoxycoumarinAntioxidant activityZ. gilletii root[108]
IsoscopletinAntispasmodic activity Z. nitidum leaves [120]
ZhebeiresinolAntispasmodic and antioxidant activitiesZ. nitidum leaves [120]
Tetracosyl ferulate Anti-thrombotic activity Different parts of Z. bungeanum[115]
SchinicoumarinAnti-thrombotic activity Z. schinifolium bark [121]
AcetoxyauraptenAnti-thrombotic activity Z. schinifolium bark [121]
EpoxycollininAnti-thrombotic activity Z. schinifolium bark [121]
SchininallylolAnti-thrombotic activity Z. schinifolium bark [121]
SchinilenolAnti-thrombotic activity Z. schinifolium bark [121]
SchinindiolAnti-thrombotic activity Z. schinifolium bark [121]
AuraptenAnti-thrombotic activity Z. schinifolium bark [121]
CollininAnti-thrombotic activity Z. schinifolium bark [121]
EpoxyauraptenAnti-thrombotic activity Z. schinifolium bark [121]
HydrangetinAnti-thrombotic activity Z. schinifolium bark [121]
UmbelliferoneAnti-thrombotic activity Z. schinifolium bark [121]
AcetoxycollininAnti-thrombotic activity Z. schinifolium bark [121]
8-methoxyanisocoumarin HAnti-thrombotic activity Z. schinifolium root bark [122]
Anisocoumarin HAnti-thrombotic activity Z. schinifolium root bark [122]
PlatydesmineAnti-thrombotic activity Z. schinifolium root bark [122]
AmottianamideAnti-thrombotic activity Z. schinifolium root bark [122]
Tetracosyl ferulateAnti-thrombotic activity Z. schinifolium root bark [122]
7-[(E)-7′-hydroxy-3′,7′-dimethylocta-2′,5′-dienyloxy] coumarin Anti-thrombotic activity Z. schinifolium root bark [122]
Table
Table 5. Terpenes and their derivatives isolated from Zanthoxylum species with anti-obesity, antioxidant, anti-thrombotic and hepatoprotective activities.
Table 5. Terpenes and their derivatives isolated from Zanthoxylum species with anti-obesity, antioxidant, anti-thrombotic and hepatoprotective activities.
Isolated CompoundBiological ActivitiesPart of PlantRefs.
IsobauerenolAnti-obesity activityZ. heitzii stem bark [112]
LimoneneAntioxidant activityZ. armatum leaves essential oil[123]
Germacrene D Antioxidant activityZ. zanthoxyloides root and stem bark[104]
MyrceneAntioxidant activityZ. gilletti leaves [109]
4′-(4”-hydroxy-3”-methylbutyloxy)-2-phenylethanolAntioxidant activityF. zanthoxyloides root bark [62]
CymeneAntioxidant activityZ. armatum leaves essential oil [123]
α-CopaeneAntioxidant activityZ. armatum leaves essential oil [123]
γ-TerpineneAntioxidant activityZ. armatum leaves essential oil [123]
BornylacetateAntioxidant activityZ. armatum leaves essential oil [123]
CampheneAntioxidant activityZ. armatum leaves essential oil [123]
LinaloolAntioxidant activityZ. armatum leaves essential oil [123]
β-OcimeneAntioxidant activityZ. armatum leaves essential oil [123]
transcaryophylleneAntioxidant activityZ. armatum leaves essential oil [123]
Germacrene Antioxidant activityZ. armatum leaves essential oil [123]
α-Terpinolene Antioxidant activityZ. armatum leaves essential oil [123]
β-AmyrenoneAnti-thrombotic activityDifferent parts of Z. bungeanum[115]
β-AmyrinAnti-thrombotic activity Different parts of Z. bungeanum[115]
FriedelinAnti-thrombotic activity Z. schinifolium bark [122]
LupeolHepatoprotective effectZ. armatum root [86]
Table
Table 6. Lignans and their derivatives isolated from Zanthoxylum species with anti-inflammatory, antispasmodic, anti-thrombotic, antioxidant, cardioprotective and antiulcer activities.
Table 6. Lignans and their derivatives isolated from Zanthoxylum species with anti-inflammatory, antispasmodic, anti-thrombotic, antioxidant, cardioprotective and antiulcer activities.
Isolated CompoundBiological ActivitiesPart of PlantRefs.
Zanthpodocarpins A and B,Anti-Inflammatory activityZ. bungeanum barks[63,65]
EudesminAnti-inflammatory activityZ. bungeanum barks[63,65]
(1R,2R,5R,6S)-2-(3,4-Dimethoxyphenyl)-6-(3,4-dihydroxyphenyl)-3,7-ioxabicyclo[3.3.0]octaneAnti-inflammatory activityZ. bungeanum barks[63,65]
Magnone AAnti-inflammatory activityZ. bungeanum barks[63,65]
rel-(1R,5R,6S)-6-(4-hydroxy-3-Methoxyphenyl)-3,7-dioxabicyclo[3.3.0]octan-2-one Anti-inflammatory activityZ. bungeanum barks[63,65]
Dimethoxysamin Anti-inflammatory activityZ. bungeanum barks[63,65]
Zanthpodocarpins C-H Anti-inflammatory activityZ. bungeanum barks[63,65]
FargesinAnti-inflammatory activityZ. armatum root and stem[124]
KobusinAnti-inflammatory activityZ. armatum root and stem[124]
Planispine AAnti-inflammatory activityZ. armatum root and stem[124]
Pinoresinol-di-3,3-dimethylallylAnti-inflammatory activityZ. armatum root and stem[124]
PinoresinolAntispasmodic activity Z. nitidum leaves [120]
MedioresinolAntispasmodic activity Z. nitidum leaves [120]
Piperitol-3,3-dimethylallyl etherAnti-thrombotic activity Z. nitidum stem bark[110]
(+)-SesaminAntioxidant and chemopreventive activitiesZ. zanthoxyloides fruits[58]
Hydroxy-α-sanshoolCardioprotective activityZ. bungeanum fruits [125]
hydroxy-β-sanshoolCardioprotective activityZ. bungeanum fruits [125]
L-sesamin Antiulcer activityZ. nitidum root [56]
Table
Table 7. Amides isolated from Zanthoxylum species and their biological activities.
Table 7. Amides isolated from Zanthoxylum species and their biological activities.
Isolated CompoundClass of CompoundBiological ActivitiesPart of PlantRefs.
Zanthoxylum amides with anti-inflammatory, antioxidant, antispasmodic, hypolipidemic and neuroprotective activities
Zanthoamide AAlkylamide Anti-inflammatory activityZ. bungeanum pericarps [126]
Zanthoamide BAlkylamide Anti-inflammatory activityZ. bungeanum pericarps [126]
Zanthoamide CAlkylamide Anti-inflammatory activityZ. bungeanum pericarps [126]
Zanthoamide DAlkylamide Anti-inflammatory activityZ. bungeanum pericarps [126]
Bugeanumamide AAlkylamide Anti-inflammatory activityZ. bungeanum leaves [127,128]
TessmamideAromatic amideAntioxidant activityZ. gilletii root [108]
RobustinAromatic amideAntioxidant activityZ. gilletii root [108]
IntegrifoliodiolAromatic amideAntioxidant activityZ. gilletii root [108]
LupenoneAromatic amideAntioxidant activityZ. gilletii root [108]
Zanthoamide GAlkalimide Antioxidant activityZ. zanthoxyloides fruits[58]
Zanthoamide HAlkalimide Antioxidant activityZ. zanthoxyloides fruits[58]
Zanthoamide IAlkalimide Antioxidant activityZ. zanthoxyloides fruits[58]
(R)-tembamideBenzamideAntispasmodic activity Z. fagara stem bark [129]
O-methyltembamideBenzamideAntispasmodic activity Z. fagara stem bark [129]
4-methoxyquinolin-2-oneCyclic amideAntispasmodic activity Z. nitidum leaves [120]
β-, γ- and hydroxy-β-sanshoolAmideHypolipidemic effectsZ. bungeanum fruit [130]
zanthoamide E and FAlkyamideNeuroprotective activityZ. bungeanum pericarps [126]
ZP-amide A-EAlkyamideNeuroprotective activityZ. bungeanum pericarps [126]
TetrahydrobungeanoolAlkyamideNeuroprotective activityZ. bungeanum pericarps [126]
(2E,7E,9E)-N-(2-hydroxy-2-methylpropyl)-6,11-dioxo-2,7,9-dodecatrienamide AlkyamideNeuroprotective activityZ. bungeanum pericarps [126]
Table
Table 8. Phytosterols and their derivatives, phenol and phenolic acids, tannins, fatty acids, phenylpropanoids and steroid isolated from Zanthoxylum species with their biological activities.
Table 8. Phytosterols and their derivatives, phenol and phenolic acids, tannins, fatty acids, phenylpropanoids and steroid isolated from Zanthoxylum species with their biological activities.
Isolated CompoundBiological ActivitiesPart of PlantRefs.
Zanthoxylum phytosterols and their derivatives
StigmasterolAntioxidant activities Z. paracanthum stem bark[74,131]
β-sitosterolAntioxidant and anti-thrombotic propertiesZ. budrunga leaves and different parts of Z. bungeanum[33,108,115,132]
β-sitostenone Antioxidant and anti-thrombotic activitiesDifferent parts of Z. bungeanum [115]
Zanthoxylum phenylpropanoids
4′-(3′′-methylbut-2′′-enyloxy)-3-phenylpropanolAntioxidant activityF. zanthoxyloides root bark [62]
N-trans-coumaroyl tyramineAntispasmodic activity Z. nitidum leaves [120]
Zanthoxylum phenol and phenolic acids
2-Methoxy-4-hydroxylphenyl-1-O-α-L-rhamnopyranosyl-(1′′→6′)-β-D-glucopyranosideAnti-inflammatory activityZ. armatum stem extract [116]
CuspidiolAntioxidant activityF. zanthoxyloides root bark [62]
DihydrocusidiolAntioxidant activityF. zanthoxyloides root bark [62]
Caffeic acidAntioxidant activityZ. zanthoxyloides stem bark [106]
Chlorogenic acidAntioxidant activityZ. zanthoxyloides stem bark [106]
HydrocuspidiolAntioxidant activityF. zanthoxyloides root bark [62]
Zanthoxylum tannins
1H-[1,2,4]-oxadiazolo-[4,3-α]-quinoxalin-1-one Anti-hypertensive activityZ. bungeanum leaves [133]
Zanthoxylum long-chain fatty acids
Hexadecanoic acidAntioxidant activityZ. zanthoxyloides root and stem bark[103]
Zanthoxylum quinolones
FlindersineAnti-thrombotic activity Z. nitidum stem bark[110]
4-methoxy-1-methyl-2-quinoloneAnti-thrombotic activity Z. nitidum stem bark[110]
4-methoxy-1-methyl-2(1H)-quinolinone Not specifiedZ. davyi stem bark[42]
Table
Table 9. Other chemicals isolated from Zanthoxylum species and their biological activities.
Table 9. Other chemicals isolated from Zanthoxylum species and their biological activities.
Isolated CompoundClass of CompoundBiological ActivitiesPart of PlantRefs.
AtanineAlanine derivativeAntioxidant activityZ. zanthoxyloides fruits[58]
115kDa glycoproteins GlycoproteinAnti-inflammatory activityZ. bungeanum leaves[134]
IsoplatydesmineAromatic compoundsAntioxidant activityZ. zanthoxyloides fruits[58]
N-methylatanineCarboxylic acidAntioxidant activityZ. zanthoxyloides fruits[58]
N-Benzoyltyramine methyl etherDimethyl etherAntioxidant activityZ. gilletii root [108]
DecanalMedium-chain aldehydesAntioxidant activityZ. zanthoxyloides root and stem bark[105]
4-(methylamino)-benzoic acidPhenolic acidAntioxidant and antiulcer activitiesZ. syncarpum branches[135]
N-benzoyl-L-PhenylalaninolPhenylalanine derivativeAntispasmodic activity Z. nitidum leaves [120]
4-methoxy-1-methyl-2-quinoloneQuinoloneAnti-thrombotic activity Z. nitidum stem bark[110]
Isovanillic acid Phenolic acidCardioprotective activityZ. bungeanum fruits [125]
4-methoxy-1-methyl-2(1H)-quinolinone) QuinoloneNot specifiedZ. davyi stem bark[42]
Table
Table 10. Summary of biological activities of Zanthoxylum species.
Table 10. Summary of biological activities of Zanthoxylum species.
Plant Species and Part UsedTest SubstanceResultsRefs.
Antioxidant properties
Z. budrunga seedsPolyphenol-rich crude ethanol extractGood DPPH radical scavenging effect (IC50 value of 82.60 μg/mL) compared to ascorbic acid (IC50 value of 12.58 μg/mL) and ferric reducing power relative to ascorbic acid standard[179]
Z. bungeanum pericarp and seedMagnoflorine and arbutin isolated from themMagnoflorine and arbutin showed weak antioxidant activities [125]
Z. bungeanum fruitHyperoside and quercitrin isolated from the fruit Strong antioxidant and radical scavenging activities[133]
Z. armatum leavesEssential oilGood DPPH radical scavenging activity (IC50 = 27 μg/mL) relative to ascorbic acid (IC50 = 15.0 μg/mL)[123]
Z. armatum leaves crude methanol extract, Essential oil and ethyl acetate fraction of the crude extractRadical scavenging, ferric reducing and divalent metal chelating potentials[85]
Z. zanthoxyloides fruits, leaves, stems, trunk barks, and root barksmethanol extractHigh radical scavenging and ferric reducing properties[103,180]
Z. capense leaves Acetone extract Good antioxidant and radical scavenging activities [19]
Z. syncarpum Tull. Branchescrude ethanol extract, its alkaloidal fraction and 4-(methylamino)-benzoic acid isolated from itThe crude extract and its alkaloidal fraction inhibited DPPH radical scavenging activities with IC50 values of 140.29 μg/mL and 56.17 μg/mL, respectively relative to quercetin (IC50 = 4.77 μg/mL). The crude extract, the alkaloidal fraction and 4-(methylamino)-benzoic acid potently inhibited hydrochloric acid-induced corrosion; 4-(methylamino)-benzoic acid showed the best corrosion inhibition [135]
Z. leprieurii stem bark hydroethanol and aqueous Good antioxidant activity[15]
Anti-diabetic effects
Z. chalybeum stem bark and root barkAqueous extractHypoglycemic activity and protected β-cells from damage[155,157]
Z. armatum bark Aqueous-ethanol extractAnti-diabetic and hypoglycemic activities[162]
Z. zanthoxyloides leavesDietary formulationExhibited good anti-diabetic, hepatoprotective and hypolipidemic effects against alloxan toxixity in rats[196]
Z. armatum leaves Aqueous extractHypoglycemic and inhibition of lipase, α-amylase and α/β-glucosidases activities[160]
Z. armatum fruits, bark and leaves methanol extractSuppressed glucose level, increased insulin secretion via KATP channel and inhibited β-glucosidases activities (94% by bark extract, 97% by leaf extract and 84% by fruits extract[161]
Gatro-protective effects
Z. zanthxyloides root barkEthanol extractInhibited ulcer index by 71% and 85% at 250 and 500 mg/kg via inhibition of cholinergic, nicotinic and histaminic receptors[135]
Z. nitidum stem bark aqueous extract inhibited ulcer by 31% and 55% at 100 and 200 mg/kg by inhibiting gastric secretion[170]
Z. nitidum roots, stems and leavesAqueous extracts and total alkaloid extractgastroprotective effect by increasing NO, prostaglandin E2 and antioxidant status as well as reducing lipid peroxidation[55]
Z. nitidum root aqueous extract Inhibition of gastric acid secretion and cytotoxic against H. pylori by inhibiting its urease activity[56]
Z. rhoifolium stem barks ethanol extractAntiulcer activity by antioxidant protection of the mucosa from free radical-mediated oxidation, activation of KATP channel and increase in NO availability[173]
Hepatoprotective effects
Z. bungeanum fruitsGlycoproteinHepatoprotective properties by mechanisms related to anti-oxidative and radical scavenging properties[63]
Z. bungeanum leaves crude methanol extractHepatoprotective properties by antioxidant activity and inhibition of lipid peroxidation and aniline hydroxylase activity[174]
Z. armatum leaves crude methanol extractInhibited hepatic damage by antioxidant mechanism[86,175]
Z. armatum fruit aqueous extractProtected liver cells from damage by antioxidant status elevating catalase and vitamin C levels in serum and non-protein thiols in liver homogenate and lowering of malondialdehyde and liver enzyme levels in serum[177]
Lipid-lowering effects
Z. bungeanum fruit and pericarppetroleum ether, Crude ethanol extract, ethyl acetate and n-butanol fractionsHypolipidemic activity by inhibiting in vivo lipid synthesis and increasing breakdown[118,178]
Z. bungeanum fruit Ethanol extractInhibited lipid synthesis, transport and storage in both 3T3-L1 adipocytes and high fat diet-induced obese mouse[179]
Z. heitzii stem bark aqueous extractReduced lipid levels by lipid synthesis inhibition and increasing the breakdown, protected cells from hyperlipidemia damages [89]
Anti-hypertensive effects
Z. bungeanum leaves crude methanol extract and its aqueous, n-hexane, ethyl acetate and n-butanol fractions Induced vasorelaxation of smooth muscles by acting through SOCC- and Akt-eNOS-sGC-cGMP signaling in isolated aorta[208]
Z. gilletii stem barks aqueous extactsReduced systolic and diastolic blood pressures, pulse pressure and heart rate by over 75% through NO signaling[51,148]
Cardioprotective effects
Z. acanthopodium fruit ethyl acetate extract Protected the myocardium from doxorubicin-generated cardiac damage[140]
Z. bungeanum fruitscrude aqueous and alcoholic extracts and hydroxy-α-sanshool, hydroxy-β-sanshool, xanthoxylin, mikanin, hyperin, isoquercitrin, rutin, myricetin, myricitrin, quercitrin and isovanillic acid isolated from themImproved breathing rate in cultured cardiac cells by inducing calcium uptake and modulating sarcoplasmic reticulum Na+/K+- and Ca2+-ATPase activities[125]
Z. chalybeum root barkaqueous extractAttenuated diabetes-related myocardial dysfunction[157,190]
Neuro-protective and Alzheimer′s disease modulatory effects
Z. bungeanum pericarps crude extract and alkylamides isolated from itPotent neuritogenic activity[126]
Z. capense root methanol and ethyl acetate extracts Inhibition of rotenone-elicited neuronal injury in SH-SY5Y neuroblastoma cells [151]
Z. bungeanum leaves crude methanol extract and flavonoid-rich fraction Good antioxidant and radical scavenging activities and Strongly inhibited hydrogen peroxide-induced neuronal cell damage in neuronal PC12 cells[127]
Z. heitzii fruits and barks syringic acid isolated from themPotent neuroprotective activity against ischaemia/reperfusion (OGD/R) neuronal injury[153]
Z. schreberi bark Crude extract and berberine, chelerythrine and columbamine from itStrongly inhibited acetylcholinesterase and butyrylcholinesterase[11]
Z. monophylum bark Crude extract and berberine, chelerythrine and columbamine isolated from itStrongly inhibited acetylcholinesterase and butyrylcholinesterase[11]
Anti-inflammatory and antinociceptive effects
Z. austrosinense rootAlkaloids isolated from ethanol extractStrongly inhibited NO production in LPS-activated mouse macrophage RAW 264.7 cells (IC50 values = 0.89–9.62 μM)[114]
Z. budrunga seedscrude ethanol extractThe extract at 250 and 500 mg/kg inhibited acetic acid-induced writhings in mice by 65.28% and 74.30%, respectively relative to 81.95% inhibition by diclofenac sodium that served as standard. Similarly, the extract at the same doses time and dose-dependently inhibited hot plate induced pain at latency time slightly lower than morphine that served as standard.[203]
Z. capense leaves Acetone extract Good anti-inflammatory activity by inhibiting 15-lipoxygenase activity in vitro and suppressed nitric oxide synthesis in activated RAW 264.7 macrophage by 33–86% at 3.12–32 μg/mL[11]
Z. zanthoxyloides rootaqueous extractStrongly inhibited proteases and membrane damage induced by hypotonic solution[195]
Z. armatum roots and stems Ethanol extract and ethyl acetate fraction Demonstrated good anti-inflammatory activities against several models of inflammation[198]
Z. nitidum root and stem Methanol extractSuppressed feeling of both acute and chronic pain as well as inhibited both acute and chronic inflammation in both in vivo and in vitro models [119]
Z. rhetsa stem barkmethanol extractModerately inhibited acetic acid-generated writhings in mice by 47.82% and 58.89% at 250 and 500 mg/kg, respectively compared to 67.30% by reference drug, aspirin at 100 mg/kg[202]
Z. budrunga root barkethanol extractAt 250 and 500 mg/kg doses, the ethanol extract significantly increased the latency time of response to hot plate induced pain (5.80 and 6.81 s) relative to control (3.29 s) and morphine (9.60 s). The extract potently inhibited acetic acid-provoked writhings in mice by 64.58% and 77.43% at 250 and 500 mg/kg, respectively relative to 81.9% by diclofenac sodium[203]
Z. bungeanum pericarps ethanol extract and amides isolated from itGood anti-inflammatory activities by inhibiting NO production by LPS-stimulated RAW264.7 macrophages[124,197,198,199,200,201,202,203,204,205,206,207,208],
Anti-asthmatic effect
Z. bungeanum seed Essential oilInhibited nitric oxide production and suppressed pulmonary injury and infiltrations of inflammatory cells by inhibiting protein level and gene expression of inflammatory mediators and their receptors[209]
Anti-arthritic effects
different parts of Z. bungeanumEthanol extractInhibited monosodium idoacetate-induced osteoarthritic inflammation and pain as follows: stalks (65%), roots (11.8%), twigs (84.7%), fruits (72.8%) and leaves (91.6%) through inhibition of protein level and mRNA expression of iNOS and COX-2[201]
Z. bungeanum cakeZ. bungeanum-cake-separated moxibustionInhibited Freund’s complete adjuvant-induced rheumatoid arthritis by preventing edema formation, histological markers of inflammatory damages to the tissues and levels of pro-inflammatory cytokines (IL-1β and TNF-α) in serum [63]
Anti-thrombotic effect
Z. schinifolium barkCoumarins, alkaloids and triterpenoids isolated from chloroform fractionSignificantly inhibited platelet aggregatory response[179]
Z. schinifolium root barkExtract and 30 isolated compoundsSignificantly inhibited collagen, arachidonic acid and platelet-activating factor-induced platelet aggregation [122]
Z. nitidum var. tomentosum rootsEthanol extract and toddalolactone isolated from itStrongly inhibited PAI-1 and PAI-1-induced clot formation and induced breakdown of preformed clot in vitro. toddalolactone also inhibited ferric chloride-generated clot formation and hepatic necrosis and increased bleeding time in mice[13]
Anti-spasmodic effect
Z. fagara stem barkCrude ethanol extract Suppressed muscle spasm and modulate muscle tone and contraction in isolated rat ileum, in vitro[114]
Z. armatum fruit, bark and leavesMethanol extractInhibited butyryl cholineesterase activity by 51%, 83% and 38%, respectively and potently relaxed precontracted rabbit jejunum strips, intestine, trachea and thoracic aortic rings[207]
Z. rhoifolium leavesalcoholic and aqueous extracts Suppressed muscle spasm and modulate muscle tone and contraction in isolated rabbit duodenum, in vitro [208]
Oesteoprotective effect
Z. piperitum fruitAqueous-ethanol extract Exerted osteoprotective effects by inhibited the activation of c-fos/NFATc1/NF-κB pathway in osteoclast of receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoporosis in ovariectomized mice[210]
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Okagu, I.U.; Ndefo, J.C.; Aham, E.C.; Udenigwe, C.C. Zanthoxylum Species: A Comprehensive Review of Traditional Uses, Phytochemistry, Pharmacological and Nutraceutical Applications. Molecules 2021, 26, 4023. https://doi.org/10.3390/molecules26134023

AMA Style

Okagu IU, Ndefo JC, Aham EC, Udenigwe CC. Zanthoxylum Species: A Comprehensive Review of Traditional Uses, Phytochemistry, Pharmacological and Nutraceutical Applications. Molecules. 2021; 26(13):4023. https://doi.org/10.3390/molecules26134023

Chicago/Turabian Style

Okagu, Innocent Uzochukwu, Joseph Chinedu Ndefo, Emmanuel Chigozie Aham, and Chibuike C. Udenigwe. 2021. "Zanthoxylum Species: A Comprehensive Review of Traditional Uses, Phytochemistry, Pharmacological and Nutraceutical Applications" Molecules 26, no. 13: 4023. https://doi.org/10.3390/molecules26134023

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