Plant ingredients in Thai food: a well-rounded diet for natural bioactive associated with medicinal properties
- Published
- Accepted
- Received
- Academic Editor
- Ravinder Kumar
- Subject Areas
- Food Science and Technology, Plant Science
- Keywords
- Bioactive compounds, Thai plants, Food, Anti-inflammatory, Antibacterial, Antiviral agents
- Copyright
- © 2023 Buathong and Duangsrisai
- Licence
- This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
- Cite this article
- 2023. Plant ingredients in Thai food: a well-rounded diet for natural bioactive associated with medicinal properties. PeerJ 11:e14568 https://doi.org/10.7717/peerj.14568
Abstract
Background
Seeking cures for chronic inflammation-associated diseases and infectious diseases caused by critical human pathogens is challenging and time-consuming. Even as the research community searches for novel bioactive agents, consuming a healthy diet with functional ability might be an effective way to delay and prevent the progression of severe health conditions. Many plant ingredients in Thai food are considered medicinal, and these vegetables, herbs, and spices collectively possess multiple biological and pharmacological activities, such as anti-inflammatory, antimicrobial, antidiabetic, antipyretic, anticancer, hepatoprotective, and cardioprotective effects.
Methodology
In this review, the selected edible plants are unspecific to Thai food, but our unique blend of recipes and preparation techniques make traditional Thai food healthy and functional. We searched three electronic databases: PUBMED, Science Direct, and Google Scholar, using the specific keywords “Plant name” followed by “Anti-inflammatory” or “Antibacterial” or “Antiviral” and focusing on articles published between 2017 and 2021.
Results
Our selection of 69 edible and medicinal plant species (33 families) is the most comprehensive compilation of Thai food sources demonstrating biological activities to date. Focusing on articles published between 2017 and 2021, we identified a total of 245 scientific articles that have reported main compounds, traditional uses, and pharmacological and biological activities from plant parts of the selected species.
Conclusions
Evidence indicates that the selected plants contain bioactive compounds responsible for anti-inflammatory, antibacterial, and antiviral properties, suggesting these plants as potential sources for bioactive agents and suitable for consumption for health benefits.
Introduction
Since the pandemic of Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) began in 2019, searching for new potential antiviral agents and prophylactics has driven priorities in public health research and the scientific community. Furthermore, treatment failure, drug side effects, and resistance have broadly inspired a shift in direction to investigating natural plant products as sources of effective bioactive agents. This updates a previous compilation of 207 plant species reported as having antiviral activity against essential and clinically significant viruses such as human immunodeficiency virus (HIV), herpes simplex virus (HSV), influenza, and hepatitis C (Mohan et al., 2020b).
Edible plants have the advantages of featuring milder toxicity profiles and being easy to access. In Indian cuisine, 38 edible plant species used as food or nutraceuticals have shown anti-retroviral activity, some of which also possess anti-inflammatory, immunomodulatory, or angiotensin-converting-enzyme (ACE) inhibitory activity (Patel et al., 2021). Herbal medicine is also a potent source of compounds with therapeutic properties. Antioxidant and antiviral potential has also been demonstrated in a summary of 18 herbal antimicrobial agents including clove, portulaca, tribulus, eryngium, cinnamon, turmeric, ginger, thyme, pennyroyal, mint, fennel, chamomile, burdock, eucalyptus, primrose, lemon balm, mallow, and garlic (Parham et al., 2020). Some similar articles have also been published on selected plant species. For instance, Allium cepa (Amaryllidaceae) juice, methanolic extract, and constituents like allicin, quercetin, and allyl methyl disulfide have shown anti-inflammatory effects in different models and with different mechanisms of action (Marefati et al., 2021). A review article of different plant parts, extraction solvents, and seed oil of Coriandrum sativum (Apiaceae) experimentally demonstrated anti-inflammatory effects in macrophages, mice, and rats (Sari, Bellatasie & Ifora, 2021). A trypsin inhibitor protein from seed of Tamarindus indica (Fabaceae) is proposed to have utility for inhibiting proteases related to SAR-CoV-2 infection in the worsened inflammatory condition in obesity (de Morais et al., 2021). Curcumin from Curcuma longa (Zingiberaceae) is also proposed as a potential prophylactic therapeutic for COVID-19 due to its observed antiviral activity against ten types of enveloped viruses that cause human diseases combined with an immunomodulatory effect (Thimmulappa et al., 2021). Additionally, xanthones in many plant species, including Garcinia cowa (Clusiaceae), can potentially treat inflammatory skin diseases through different mechanisms (Gunter et al., 2020).
Alongside an active lifestyle, a healthy and functional diet is of interest for maintaining and promoting well-being to prevent, delay, and even treat ailments. That is, functional food may help to boost the immune system, reduce risk of noncommunicable diseases, and improve memory or physical condition (Topolska, Florkiewicz & Filipiak-Florkiewicz, 2021). Several edible and medicinal plants serve as daily elements of the diet in traditional Thai cuisine, which emphasizes aromatic components, flavor, and appearance and utilizes a range of preparation methods such as spicy salads, steaming or boiling, stir-frying, frying, and chili pastes for a dip. Moreover, Thai cuisine includes many coconut-milk-based curry pastes with slightly different compositions like red curry, sweet green curry, yellow curry, nutty curry, a fusion of Thai and Indian styles (Massaman curry), and non-coconut-milk based curry pastes such as the famous Tom Yam (hot and sour soup with or without coconut milk), Tom Kah (coconut milk with galangal rhizome and kaffir lime leaves), and Gaeng Som (sour fish curry paste soup) (Kanchanakunjara, Chantachon & Koseyayotin, 2017; Khanthapok & Sukrong, 2019). The unique combination of vegetables, herbs, and spices used in Thai dishes makes Thai food an excellent example of a healthy diet. Notably, many of these plants have also been used in traditional medicine over generations to maintain health or relieve and cure ailments and infectious diseases. With the increasing problems posed by antimicrobial resistance, viral diseases, and inflammatory conditions related to various symptoms and diseases, the ingredients and medicinal plants in Thai dishes could comprise a valuable potential resource for the discovery of bioactive compounds with anti-infective and protective effects.
Here, we highlight different plant species and parts used in Thai food and traditional medicine simultaneously, as part of a functional diet and as phytomedicine; we also discuss their important metabolites, therapeutic uses, and biological and pharmacological activities. Furthermore, this review summarizes an update of recent research papers on plant extracts and, in some instances, isolated compounds that have demonstrated anti-inflammatory effects and antibacterial activity against selected critical antibiotic-resistant bacteria (Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae) or antiviral activity against clinically significant human viruses such as influenza virus, herpes simplex virus, Zika virus, and SARS-CoV-2.
The present review provides an easy-to-access list of edible and medicinal plants as a database, which is vital in developing further applications in clinical practice and drug discovery to comply with the UN goal of sustainable development to promote good health and well-being. Moreover, these plants might be integrated into food processing and manufacturing or added into any diet regimen as ingredients that promote and restore health. Our review can guide further research and offers highly interesting material for other scientists working on several aspects of plant-related life sciences, natural products, and the international plant science community. Thai food is complex, and its plant ingredients are abundant in tropical and subtropical regions; that is, the plants discussed here are not specific to the South-East Asia region. To the best of our knowledge, our work represents one of the most comprehensive indexes of diverse plants from a single cuisine that feature bioactivities that impact human health. It can inform and increase public awareness about the importance of ongoing research activities in plant science, phytochemistry, and pharmacognosy.
Survey methodology
For the development of this review, globally-recognized names of the plant materials selected based on their use in Thai food and folk medicine were obtained from Plants of the World Online (POWO; https://powo.science.kew.org/) and the International Plant Names Index (IPNI; https://www.ipni.org/). Related literature dated from 2017 to 2021 was then sourced from scientific databases including PUBMED, Science Direct, and Google Scholar by searching with the term “Plant name” followed by the keyword “Anti-inflammatory” or “Antibacterial” or “Antiviral.” After carefully considering the obtained literature, we took only those publications that fit our scope of review. We proceeded to develop our database and produce this review. The compiled plant species and associated phytochemicals presented here have demonstrated the most promising health benefits and advantages with regard to targeting lead compounds.
An overview of culinary herbs, spices, and medicinal plants in thai food
We summarized a selection of 69 species (33 families) from edible and medicinal plants used in Thai food, and also Zingiber cassumunar in the family Zingiberaceae. The selection covers plant parts consumed as vegetables or as ingredients in the preparation of many Thai dishes. Based on several phytochemical studies, all of the selected plant species are potential sources of bioactive compounds in various classes; Table 1 presents the main chemical compositions of the different plant families and genera.
Family | Botanical name | Local name | Food preparation | Part | Phytochemicals | References |
---|---|---|---|---|---|---|
Amaranthaceae | Suaeda maritima (L.) Dumort. | Cha kram ชะคราม |
Fresh, boiled, seasoning | Leaves | Essential oil, fatty acids, campesterol (steroid), ethanone (phenolic compound) | Nayak et al. (2018) |
Amaryllidaceae | Allium ascalonicum L. | Hom daeng หอมแดง | Flavoring or seasoning and one of the main components in all Thai curries | Bulb | Organosulfur compounds (allin, allicin), flavonoids, phenolic compounds (quercetin, kamferal) | Ounjaijean et al. (2018) |
Allium cepa L. | Hom yai หอมใหญ่ |
Fresh, flavoring | Bulb | Organosulfur compounds, polyphenols, saponins, flavonoids quercetin, quercetin glycosides, flavonols | Kothari, Lee & Kim (2020), Marefati et al. (2021) | |
A. cepa var. aggregatum G. Don | Ton hom ต้นหอม |
Fresh, flavoring, decorating | Bulblets, leaves | Volatile compound: allyl-propyl disulphide | Saraswathi et al. (2017) | |
Allium sativum L. | Kra thiam กระเทียม |
Flavoring agent in all types of Thai food and usually do not remove the peel entirely to remain the fragrance or used raw as thin slices | Bulb | Organosulfur compounds (alliin, allicin), γ-glutamyl cysteine derivatives | Shao et al. (2020), Rouf et al. (2020) | |
Apiaceae | Apium graveolens L. | Khuen chai คื่นช่าย |
Flavoring | Leaves, stem | Phthalides and derivatives, flavonoids: quercetin, apigenin, chrysoeriol, luteolin; glycosides, steroids, alkaloids, furocoumarins, phenols, sesquiterpenes alcohol, phenolic acids, tocopherol, terpenoids, essential oils | Salehi et al. (2019b), Emad et al. (2020), Khairullah et al. (2021) |
Centella asiatica (L.) Urb. | Bua bok บัวบก |
Fresh, beverage | Leaves | Triterpene asiaticoside, asiatic acid, madecassoside, madecassic acid | Sun et al. (2020), Hafiz et al. (2020) | |
Apiaceae | Coriandrum sativum L. | Phak chi ผักชี |
Leaves and stems are eaten fresh, root is typically mixed with garlic and pepper, seed is used in making curry paste | Whole plant | Flavonoids, essential oil, tannins, phenolics, alkaloids, terpenoids, fatty acids, sterols, glycosides | Kothalawala et al. (2020), Sari, Bellatasie & Ifora (2021) |
Cuminum cyminum L. | Yira ยี่หร่า |
Roasted seed to heighten fragrance before used as a flavoring and condiment in many curry dishes | Seed | Cuminaldehyde and cuminic alcohol, roasted seeds contain substituted pyrazines, 2-ethoxy-3-isopropylpyrazine, 2-methoxy-3-sec-butylpyrazine, 2-methoxy-3-methylpyrazine flavoalkaloids (flavonoid alkaloids) |
Srinivasan (2018), Kang et al. (2019) |
|
Eryngium foetidum L. | Phak chi farung ผักชีฝรั่ง |
Fresh, flavoring | Leaves | (E)-2-dodecenal, 13-tetradecenal, dodecanal, 2,4,5-trimethylbenzaldehyde | Thomas et al. (2017) | |
Apocynaceae | Telosma cordata (Burm. f.) Merr. | Khachon ขจร |
Boiled, stir fired, sour curry paste soup | Flower buds | Phenolics, volatile components: geraniol, beta-ionone, dihydro-beta-ionone, dihydro-beta-ionol, cis-and trans-theaspirane | Nguyen (2020) |
Basellaceae | Basella alba L. | Phak plung ผักปลัง |
Boiled, soup | Leaves | Betacyanin, carotenoids, bioflavonoids, β-sitosterol, lupeol | Chaurasiya et al. (2021) |
Caricaceae | Carica papaya L. | Malako มะละกอ |
Spicy salad “Som Tum”, sour curry paste soup | Unripe fruit | Octadecanoic acid, hexadecenoic acid, hexadecanoic acid, methyl ester, enzymes: papain, chymopapain | Sharma et al. (2020) |
Cleomaceae | Cleome gynandra L. | Phak Sian ผักเสี้ยน |
Pickled vegetable | Leaves | Methyl glucosinolate (glucocapparine), flavonoids, triterpenoids, sitosterol | Adhikari & Paul (2018) |
Clusiaceae | Garcinia cowa Roxb. ex Choisy | Cha moung ชะมวง | Leaves used in soup or stew | – | Prenylated and oxygenated xanthones | Santo et al. (2020) |
Garcinia schomburgkiana Pierre | Ma dan มะดัน |
Fruits used in soup, chili paste | – | Bixanthones (in twigs), xanthones, biphenyls, flavonoids, benzoylphloroglucinols | Do et al. (2020) | |
Cucurbitaceae | Coccinia grandis (L.) Voigt | Tum lueng ตำลึง |
Boiled, soup | Arial part, leaves |
Alkaloids, saponins, flavonoids, phenols, tannins, heptacosane, cephalandrol, β-sitosterol, cephalandrins A and B | Harshitha, Prasanthi & Ramarao (2018) |
Cucurbita moschata Duchesne | Fak Thong ฟักทอง |
Boiled, stir-fried, dessert | Pulp, | Gallic acid, protocatechuic acid, 4-hydroxybenzoic acid, vanillic acid, chlorogenic acid, caffeic acid, rutin, carotenoids, phenolic acids, flavonols | Kulczynski & Gramza-Michałowska (2019) | |
Momordica charantia L. | Mara มะระ |
Fresh vegetable, boiled, stir-fried | Fruit | Charantia (cucurbitane triterpenoids), α-momorcharin, MAP30, saponins, flavonoids, alkaloids, sterols | Villarreal-La Torre et al. (2020) | |
Lagenaria siceraria (Molina) Standl. | Nam Tao น้ำเต้า |
Boiled | Fruit | Cucurbitacin B, mucilage, sterols, terpenoids, flavonoids, saponins | Tyagi ,Sharma & Shrivastava (2017) | |
Luffa acutangular (L.) Roxb. | Bob ream บวบเหลี่ยม |
Boiled, stir-fried, soup | Unripe fruit | Flavonoids, anthraquinone, triterpenes, volatile components | Shendge & Belemkar (2018) | |
Dilleniaceae | Dillenia indica L. | Ma tad มะตาด |
Flavoring | Fruit | Betulin (pentacyclic triterpenoid), betulinic acid, cycloartenone, sterols, glycosides, saponins | Barua, Yasmin & Buragohain (2018) |
Euphorbiaceae | Phyllanthus emblica L. | Ma kham pom มะขามป้อม |
Raw or mixed with chili paste | Fruit | Flavonoids, tannins, diterpenes, gallic acid, ellagic acid, corilagin, chebulagic acid, quercetin | Jantan et al. (2019) |
Fabaceae | Acacia pennata (L.) Willd. | Cha om ชะอม |
Fried, sour curry paste | Leaves | Flavonoids: apigenin, quercetin- and kaempferol diglycoside, isorhamnetin mono-glycoside, isovitexin, flavanol glycosides, terpenoids | Aye et al. (2019), El-Taher et al. (2021) |
Clitoria ternatea L. | Anchan อัญชัน |
Colorant, beverage, fresh, stir-fried | Flower | Flavonol glycosides anthocyanins, rutin (flavone), epicatechin (flavanol); polyphenolic acids: gallic acid, protocatechuic acid, chlorogenic acid; ternatins A1-3, B1-4, C1-5, D1-3 | Gollen, Mehla & Gupta (2018), Oguis et al. (2019) | |
Neptunia prostrata (Lam.) Baill. | Phak kra ched ผักกระเฉด |
Raw, boiled, stir-fried | Leaves | Pheophorbide a, phenolic compounds, derivatives of quercetin, kaempferol, apigenin | Sagolshemcha & Singh (2017), Lee et al. (2019) | |
Leucaena leucocephala (Lam.) de Wit | Kra tin กระถิน |
Raw, boiled | Leaves | Flavones, flavonols, flavanone, flavanonol, flavonol glycosides, 1,2-benzenedicarboxylic acid, mono (2-ethylhexyl) ester, betulin, lupeol, androstan-17-one,3-ethyl-3-hydroxy-, (5à)-, 9,12,15-octadecatrienoic acid, methyl ester, (Z,Z,Z)-, betamethasone, β-sitosterol | Xu et al. (2018), Zayed, Wu & Sallam (2019) | |
Parkia speciosa Hassk. | Sataw สะตอ |
Raw, stir-fried | Seeds | Cyclic polysulfides, 1,2,4-trithiolane, propanoic acid), 3,3-thiobis-didodecyl ester, phenols, flavonoids, alkaloids, terpenoids, fatty acids | Chhikara et al. (2018), Saleh et al. (2021) | |
Sesbania grandiflora (L.) Pers. | Dok Kae ดอกแค |
Boiled and sour curry paste | Flower | Flavonoids, tannins, anthraquinones, steroids, terpenoids | Mohiuddin (2019) | |
Senna siamea (Lam.) H.S.Irwin & Barneby | Khilek ขี้เหล็ก |
Boiled and then cooked with curry and coconut milk | Leaves | Polyphenols, anthraquinone, anthocyanins, alkaloids, cardiotonic glycosides, saponins, steroids, terpenoids | Ntandou et al. (2018) | |
Fabaceae | Tamarindus indica L. | Ma kham มะขาม |
Unripe fruit juice used as flavoring in Pad Thai, sour curry paste soup, tamarind sauce | Fruit | Alkaloids, flavonoids, tannins, phenols, saponins, triterpenoids, fatty acids, steroids | Komakech et al. (2019) |
Gnetaceae | Gnetum gnemon L. | Phak lueng ผักเหลียง |
Stir-fried | Leaves | 2,3-dihydroxypropyl icosanoate, oleic acid, ursolic acid, phenylheptanoid gnetumal, callyspinol, cassipourol, (+)-dehydrovomifoliol, p-coumaric acid, ferulic acid | Dutta et al. (2018), Le et al. (2020) |
Hypericaceae | Cratoxylum formosum (Jacq.) Benth. & Hook.f. ex Dyer | Phak tiu ผักติ้ว |
Soup | Leaves root |
Vismiaquinone, naringenin and 2,3-trans-dihydro-kaempferol Xanthones, anthraquinones, triterpenes |
Juanda et al. (2019), Rodanant et al. (2017) |
Lamiaceae | Mentha × cordifolia Opiz ex Fresen. | Saranae สะระแหน่ |
Flavoring, raw, garnish | Leaves | Volatile oil: monoterpenoids like carvone, limonene, menthone, menthol, pulegone, dihydrocarveol, s-carvone | Sevindik (2018) |
Ocimum sanctum L. | Kaphrao กระเพรา |
Flavoring | Leaves | Flavones (cirsilineol, circimaritin, isothymusin, apigenin), terpenoid (carvacrol and caryophyllene) | Kaur et al. (2020) | |
Ocimum gratissimum L. | Yira ยี่หร่า |
Flavoring, raw | Leaves | Essential oils, phenolic compounds: rutin, quercetin, caffeic acid, rosmarinic acid, circhoric acid, sitosterol, ursolic acid, salvigenin, transferulic acid; tannins, saponins, flavonoids, anthraquinone glycosides | Ajayi et al. (2017), Alabi et al. (2018) | |
Ocimum × africanum Lour. | Maeng lak แมงลัก |
Flavoring, raw | Leaves | Essential oils: linalool, eugenol, 1,8-cineole, and camphor | Marrelli et al. (2020) | |
Ocimum basilicum L. | Horapha โหระพา |
Flavoring, raw | Leaves | Linalool, methyl chavicol, eugenol, bergamotene, methyl cinnamate, flavonoids, steroids, saponins, tannin | Shahrajabian, Sun & Cheng (2020) | |
Lauraceae | Cinnamomum verum J.Presl | Ob chei อบเชย |
Yellow curry, stew | Stem bark | Trans-cinnamaldehyde, p-cymene, eugenol, o-methoxycinna-maldehyde, cinnamyl alcohol, benzyl benzoate, cinnamic acid, coumarin, phenolics compounds | Schink et al. (2018), Parham et al. (2020) |
Meliaceae | Azadirachta indica A. Juss. var. siamensis Valeton | Sadao สะเดา |
Vegetable, boiled | Leaves, | Triterpenoids, nimbin, glycosides nimbanene, 6-desacetylnimbinene, nim-bandiol, nimbolide, ascorbic acid, n-hexacosanol, amino acid, 7-desacetyl-7-benzoylazadiradione, 7-desacetyl-7-benzoylgedunin, 17-hydroxyazadiradione, nimbioland; flavonoids, saponins, tannins, alkaloids, limonoids, catechins, sterols, gallic acid | Islas et al. (2020) |
Menispermaceae | Cissampelos pareira L. | Khruea ma noi เครือหมาน้อย |
leaf juice is rich of pectin used in cooking or jelly dessert | Leaves | Alkaloids: isoquinoline alkaloids, benzylisoquinoline alkaloids (lau-danosine), aporphines (nuciferine, corytuberine, bulbocarpine, nor-N-magnoflorine, flavonoids, fatty acids | Iram et al. (2017), Kumari et al. (2021) |
Tiliacora triandra Diels | Yanang ย่านาง |
Boiled with bamboo shoots and eaten as vegetable | Leaves | Phenolic compounds: gallic acid, cyanidin, quercetin, catechin; hydrocarbon compounds: phytol, 1-cyclohexenylacetic acid, oleamide, oleic acid | Weerawatanakorn et al. (2018), Pasachan et al. (2021) | |
Moringaceae | Moringa oleifera Lam. | Ma rum มะรุม |
Leaves and pods can be boiled, stir-fried, and soup | Leaves seeds |
Kaempferol, gallic acid, vanillic acid, coumaric acid, quercetin Isothiocyanate-1, glycosidic glucosinolates, isothiocyanates, nitriles, carbamates, thiocarbamates |
Saleem, Saleem & Akhtar (2020) Jaja-Chimedza et al. (2017) |
Musaceae | Musa × paradisiaca L. | Hua Plee หัวปลี |
Banana blossom is consumed raw as vegetable with “Pad Thai” and cooked | Flowers | Phenolics, flavonoids, saponins | Shubham et al. (2019) |
Myristicaceae | Myristica fragrans Houtt. | Luke Chan thet ลูกจันทน์เทศ |
Flavoring, Thai Mussaman curry | Seeds | Essential oils, terpene hydrocarbons (sabinene, pinene, camphene, p-cymene, phellandrene, terpinene, limonene, and myrcene) oxygenated terpenes (linalool, geraniol, terpineol, aromatic ethers (myristicin, elemicin, safrole, eugenol, and eugenol) | Matulyte et al. (2020), Suthisamphat et al. (2020) |
Myrtaceae | Syzygium aromaticum (L.) Merr. & L.M.Perry | Kanplu กานพลู |
Flavoring, Thai Mussaman curry | Flower buds | Essential oils, eugenol, eugenyl acetate, β-caryophyllene, glycosides, saponins, flavonoids, hidroxiphenyl propens, hidroxicinamic acids, steroids, tannins, alkaloids, terpenes | Batiha et al., (2020a) |
Syzygium cumini L. | Luke wa ลูกหว้า |
Drink, dessert, jam | Fruit | Malic acid, oxalic acid, gallic acid, tannins, anthocyanins: cyanidin di-glucosides, delphinidin, petunidin; liquitrigenin, scopoletin, umbelliferon, rosmanol | Abdin et al. (2020), Qamar et al. (2021) | |
Nymphaeaceae | Nymphaea pubescens Willd. | Bua sai บัวสาย |
Coconut milk soup or stir-fried | Stem, seeds, flower | Phenolic compounds, flavonoids, gallic acid, shikimic acid | Aimvijarn et al. (2018), Rivas-García et al. (2021) |
Pandanaceae | Pandanus amaryllifolius Roxb. | Bai tei ใบเตย |
Colorant and flavoring | Leaves | Flavonoids, phenolic acids, alkaloids | Reshidan, Abd Muid & Mamikutty (2019) |
Pedaliaceae | Sesamum indicum L. | Nga งา |
Flavoring, decorating, dessert Thai crispy rolls or “Thong Muan” | Seeds | Lignans: sesamin, sesamol, sesaminol, sesamolin; tocopherols, phytosterols, ferulic acid, 5-hydroxy coniferyl alcohol, p-hydroxyphenylacetic acid, other methoxyphenol derivatives | Deme, Narasimhulu & Parthasarathy (2018), Wu et al. (2019) |
Phyllanthaceae | Sauropus androgynus (L.) Merr. | Phak waan baan ผักหวานบ้าน |
Vegetable, boiled, stir-fried, soup | Leaves | Sterols, tannins, saponins, alkaloids, flavonoids, terpenoids, lignan glycosides, phenols, catechol, cardiac glycosides, and acidic compounds | Arif & Shetty (2020) |
Piperaceae | Piper nigrum L. | Phrik Thai พริกไทย |
Black, white, fresh green pepper | Seeds, fruit | Alkaloid: piperine and derivatives isopiperine, chavicine, isochavicine, piperanine, piperettine, piperylin A, piperolein B, pipericine; monoterpenes, sesquiterpenes | Joshi, Shrestha & Adhikari (2018), Tiwari, Mahadik & Gabhe (2020) |
Piper sarmentosum Roxb. | Chaplu ชะพลู |
Salad wrap “Miang Kham”, curry | Leaves | Elemicin, methoxyeugenol, naringenin, methyl piperate, beta-asarone, brachyamide B, piperitol, guineensine, didymin, quercetin, amurensin, hesperidin, difucol | Junairiah & Zuraidassanaaz (2020) | |
Plantaginaceae | Limnophila aromatica (Lam.) Merr. | Phak khayang ผักแขยง |
Raw, soup | Arial part | Essential oil: methyl benzoate, pulegone, limonene, (+)-trans-isolimonene, α-humulene | Dai et al. (2015) |
Poaceae | Cymbopogon citratus (DC.) Stapf | Ta khrai ตะไคร้ |
Flavoring, Tom Yum, deep-fried | Stalk | Essential oils: citral, mycrene, genariol, citronellol (cymbopogonol and cymbopogone); α-oxobisabolene, terpenoids (cymbopogonol and cymbopogone); flavonoids | Oladeji et al. (2019) |
Polygonaceae | Persicaria odorata (Lour.) Soják | Phak paw ผักแพว |
Flavoring, fresh, boiled | Leaves | Essential oils: dodecanal, decanal, cis-caryophyllene, alpha-humulene, caryophyllene oxide, humulene epoxide II, drimenol, E-15-Heptadecenal, 3, 7, 11, 15-tetramethyl-2-hexadecen-1-ol; gallic acid, apigenin, ferulic acid, quercetin, ellagic acid, p-coumaric acid | Chansiw et al. (2018), Ridzuan & Wan Salleh (2019), Řebíčková et al. (2020) |
Rutaceae | Citrus × aurantium L. | Som sa ส้มซ่า |
Fruit juice and peel are used to flavor crispy rice noodles, curry | Peels blossoms |
Essential oils: linalool, limonene Essential oils: linalool, α-terpineol, (R)-limonene, linalyl acetate |
Azhdarzadeh & Hojjati (2016), Shen et al. (2017) |
Citrus hystrix DC. | Makrut มะกรูด |
Leaves, juice, and peel is used in curry paste, flavoring, garnish | Peels leaves |
Phenolic compounds, flavones, terpenoids, mainly β-pinene, limonene, sabinene, furanocoumarins Phenolic compounds, citronellal, terpenoid agrostophillinol, α/β-pinene, limonene, terpinen-4-ol |
Kidarn et al. (2018), Anuchapreeda et al. (2020) | |
Citrus aurantifolia (Christm.) Swingle | Manao มะนาว |
Juice and peel used in flavoring, garnish, beverage | Fruit peels |
Monoterpenes like limonene, β-pinene, β-terpinene, citral; alkaloids, carotenoids, coumarins, flavonoids, phenolic acids, triterpenoids Triterpenoid limonoids; sesquiterpenes p-caryophyllene, santal-10-en-2-ol; monterpenes limonene, p-pinene, geraniol, neral, geranial, citronellal |
Jain, Arora & Popli (2020) | |
Zanthoxylum rhetsa DC. | Ma khwaen มะแขว่น |
Fruit and seed used as spice; shoot consumed as vegetable | Fruit, seeds stem, root bark |
Sabinene, 4-terpineol, germacrene, gramma-terpinene, alpha-terpinene Alkaloids: isoquinoline and quinolone |
Duangyod et al. (2020), Maduka & Ikpa (2021) |
|
Solanaceae | Capsicum frutescens L. | Phrik khinu พริกขี้หนู |
Garnishing, spicy flavoring | Fruit | Capsaicin, dihydrocapsaicin, capsiconinoids, capsinoids; saponin CAY-1 | Batiha et al. (2020b) |
Capsicum annuum L. | Phrik chifah พริกชี้ฟ้า |
Garnishing, flavoring | Fruit | Capsaicinoids (mainly capsaicin and dihydrocapsaicin); sinapoyl and feruloyl glycosides (red pepper), quercetin-3-O-l-rhamnoside (green pepper) | ||
Solanaceae | Lycopersicon esculentum Mill. | Makhuea thet มะเขือเทศ | An ingredient in papaya salad and spicy salad, soup | Fruit | Carotenoids (lycopene and β-carotenoids), phytosterols (β-sitosterol, campesterol and stigmasterol), phenolic acids (quercetin, kaempferol, narin-genin, lutein, caffeic, ferulic and chlorogenic acids) | Ali et al. (2021) |
Solanum stramoniifolium Jacq. | Ma uek มะอึก |
Component of Thai chili paste and northeastern papaya salad recipe | Fruit Root |
Phenolic compounds Alkaloids, flavonoids, tannins, triterpenes, saponins, solasodine glycoalkaloid (solamargine) |
Svobodova et al. (2017) | |
Solanum torvum Sw. | Makhuea puang มะเขือพวง |
Unripe fruit consumed as vegetable and garnish in Thai curries | Fruit Stem |
Spirostanol saponins, alkaloids, flavonoids, phenols, tannins, glycosides, tocopherol Steroidal Saponins |
Lee et al. (2017b), Darkwah et al. (2020), Lacmago et al. (2021) |
|
Zingiberaceae | Alpinia galanga L. | Kah ข่า |
Flavoring in curry paste, soup Tom Yum and Tom Kah | Rhizome | Phenolic compounds: ferulic acid, apigenin, vanillic acid, kaempferol, kaempferol-3-O-methylether, luteolin, chrysin, 1’-acetoxyeugenol acetate, 4-hydroxybenzoic acid; terpenoids: galangalditerpene A-B, 1,8-cineole, α-pinene | Khairullah et al. (2020) |
Boesenbergia rotunda (L.) Mansf. | Krachai กระชาย |
Fish dishes, raw after peeled | Rhizome | Essential oils, flavonoids, polyphenols, chalcone Boesenbergin A, diarylheptanoid panduratin A | Rosdianto et al. (2020), Mohan et al. (2020a), Kanjanasirirat et al. (2020) | |
Curcuma longa L. | Kamin ขมิ้น |
Colorant, flavoring, white turmeric is eaten as a raw vegetable | Rhizome | Polyphenol curcumin, alkaloids, flavonoids, terpenoids | Hewlings & Kalman (2017), Rahaman et al. (2021) | |
Zingiber cassumunar Roxb. | Plai ไพล |
– | Rhizome | Phenylbutenoids, curcuminoids, essential oils, quinines, phenolic compounds, sesquiterpenoids | Han et al. (2021) | |
Zingiberaceae | Zingiber officinale Rosco | Khing ขิง |
Flavoring, spice, beverages, and Thai dessert black sesame dumplings in ginger tea | Rhizome | [6]-gingerol and its derivatives, monoterpenes (phellandrene, camphene, cineole, citral, and borneol), sesquiterpenes (zingiberol, zingiberene, zingiberenol, sesquiphellandrene, s-bisabolene) | Karunakaran & Sadanandan (2019) |
Many compound classes have been screened and identified in the plant species reviewed here and found to possess various medicinal properties. For example, essential oils or volatile oils, which mainly contain terpenes and terpenoids that are known as antioxidant, antimicrobial, anti-inflammatory, antidiabetic, anticancer, and antiallergic compounds, are found in aromatic plants belonging to the families Apiaceae, Clusiaceae, Lamiaceae, Lauraceae, Myristicaceae, Myrtaceae, Rutaceae, and Zingiberaceae (Marrelli et al., 2020; Masyita et al., 2022). Likewise, the alkaloid piperine and its derivatives are found in plants of the family Piperaceae and have several documented biological activities (Tiwari, Mahadik & Gabhe, 2020). Other major classes of phenolic compounds include polyphenols, phenolic acids, flavonoids, tannins, stilbenes, lignins, lignans, and coumarins, which have shown anti-inflammatory, anti-infective, antiproliferative, and antioxidant activities (Luna-Guevara et al., 2018). Curcuminoids are another group of polyphenols found in Curcuma species of the family Zingiberaceae that have been reported as having antioxidant, anti-inflammatory, antimutagenic, antimicrobial, and anticancer properties (Hewlings & Kalman, 2017). Meanwhile, natural xanthones are an important class of compounds in Garcinia species of the family Clusiaceae that have potential for treating inflammatory skin diseases (Gunter et al., 2020). Notably, xanthones are also found in the root part of Cratoxylum formosum in the family Hyperiaceae (Table 1). Hence, non-edible parts of plants should be evaluated for their potential as additional sources of new bioactive compounds (Svobodova et al., 2017; Rodanant et al., 2017; Maduka & Ikpa, 2021). Among the 69 plant species reviewed here, the commercially used species have been thoroughly investigated for constituent bioactive substances (Jantan et al., 2019; Oyeyinka & Afolayan, 2020; Marefati et al., 2021; Sari, Bellatasie & Ifora, 2021). However, there is very little literature on some less-widely used plant species, such as Telosma cordata in the family Apocynaceae (Nguyen, 2020).
Individual plants that are also used in traditional medicine and have shown various pharmacological properties are listed in Table 2. The claimed traditional uses of the selected plants are supported by updated documentation of their pharmacological activities, including antioxidant, antimicrobial, anti-inflammatory, hypolipidemic, antihypertension, antidiabetic, and other like health benefits. In some cases, it is unclear which part of the plant is used to obtain the mentioned therapeutic effect, and there is yet insufficient comparative study of phytochemical and biological activity in different parts of a given plant species. Content of bioactive compounds might vary in different parts of the same plant and in plants of closely related genera (Buathong et al., 2019). Thus, comprehensive studies of the chemical composition and bioactive components in different plant parts and in other genera that have closed taxonomic relationships with the plants listed in this work will open more possibilities for the discovery of new sources and active compounds and hence the expansion of phytomedicine development.
Family | Botanical name | Local name | Part | Ethnomedicinal | Pharmacological properties | References |
---|---|---|---|---|---|---|
Amaranthaceae | Suaeda maritima (L.) Dumort. | Cha kram ชะคราม |
Juice leaves | Hepatitis Liver, heart, and lipid disorders |
Antiviral, hepatoprotective, anti-inflammatory, antioxidant Hepatoprotective, antioxidant |
Nayak et al. (2018), Bilal & Hossain (2019) |
Amaryllidaceae | Allium ascalonicum L. | Hom daeng หอมแดง | Bulb | Relieve fevers, flatulence, infections | Antibacterial, antivirus, anti-diabetic, antioxidant, anti-inflammation | Ounjaijean et al. (2018) |
Allium cepa L. | Hom yai หอมใหญ่ |
Bulb | Stomach diseases, throat infection, hepatitis, fever, headache, cholera, dysentery, common cold, arthritis | Antioxidant, anticancer, hypolipidemic, antidiabetic, cardioprotective, neuroprotective, antimicrobial anti-inflammatory, antiglycemic | Kothari, Lee & Kim (2020), Marefati et al. (2021) | |
Allium sativum L. | Kra thiam กระเทียม |
Bulb | Common cold, fever, coughs, asthma, wounds, prevention of infectious diseases, including sexually transmitted diseases, tuberculosis, respiratory tract | Antibacterial, anti-inflammatory, antiviral, antitumor, improvement of immunity, antioxidant, anticoagulant, protection of the liver, balancing intestinal microbiota | Hussein, Hameed & Hadi (2017), Shao et al. (2020), Rouf et al. (2020) | |
Apiaceae | Apium graveolens L. | Khuen chai คื่นช่าย |
Seeds, leaves, stems | Gout, rheumatism, urinary tract inflammation, arthritis, diuretic for stimulation of the glands, bile, kidney stones, regulate the intestines, increase appetite, prophylaxis for nerve agitation, bronchitis, hepatitis, lower blood pressure, joint problems, libido stimulant, increase breast milk secretion | Antimicrobial, antiparasitic, cardioprotective, gastroprotective, neuroprotective, hypolipidemic, anti-inflammatory, anti-infertility | Salehi et al. (2019b), Emad et al. (2020), Khairullah et al. (2021) |
Apiaceae | Centella asiatica (L.) Urb. | Bua bok บัวบก |
Leaves | Skin, pain, neurological, endocrine, cardiovascular, gastrointestinal, immune, and gynecological diseases, rheumatoid arthritis, ozaena, sore throat, ulcers, burns, leprosy, scrofula | Anti-inflammatory, anti-oxidative stress, anti-apoptotic effects, improvement in mitochondrial function | Sun et al. (2020), Hafiz et al. (2020), Ramli, Xian & Mutalib (2020) |
Coriandrum sativum L. | Phak chi ผักชี |
Whole plant | Disorders of the digestive, urinary, and respiratory systems, as well as diabetes, inflammation | Antidiabetic, diuretic, cholesterol-lowering, anticancer, anti-inflammatory, antifungal, antihelmintic | Kothalawala et al. (2020), Sari, Bellatasie & Ifora (2021) | |
Cuminum cyminum L. | Yira ยี่หร่า |
Seed | Digestive disorders, chronic diarrhoea, dyspepsia, acute gastritis, diabetes, cancer | Antidiabetic, neuroprotective, cardioprotective, chemo preventive, anti-inflammatory | Srinivasan (2018) | |
Eryngium foetidum L. | Phak chi farung ผักชีฝรั่ง |
Leaves | Diabetes, rheumatism, cold, asthma, cough, sinusitis, stomach disorders | Antioxidant, anti-proliferative, antimicrobial, anti-inflammatory, antidiabetic | Thomas et al. (2017), Prabha, Athoibi & Dsouza (2019) | |
Apocynaceae | Telosma cordata (Burm. f.) Merr. | Khachon ขจร |
Flower buds leaves |
Conjunctivitis Wound, scaby, ulcer, headache |
Antimicrobial, antidiabetic, antioxidant - |
Nguyen (2020) |
Basellaceae | Basella alba L. | Phak plung ผักปลัง |
Leaves | Wound healing, androgenic, skin problems, diarrhoea, dysentery, laxative | Anticancer, antiviral, antioxidant, anti-inflammatory, anti-cholesterol, anti-ulcer, antimicrobial, anti-hypoglycemic, antiproliferative | Chaurasiya et al. (2021) |
Caricaceae | Carica papaya L. | Malako มะละกอ |
Fruit, leaves | Dengue fever, diabetes, malaria, fungal infections, skin aging, wound healing, and cancer | Anti-inflammatory, anticancer, antioxidant, antibacterial, and antiviral | Sharma et al. (2020), Haddad et al. (2020), Kong et al. (2021) |
Cleomaceae | Cleome gynandra L. | Phak Sian ผักเสี้ยน |
Leaves seeds root |
Ticks and flea prevention, earache, eye wash Anthelmintic, coughing, applied externally for headage, stomach pain Mild reduce fever |
Anti-inflammatory, antioxidant, anticancer, immunomodulator, antidiabetic | Adhikari & Paul (2018), Kanimathi et al. (2019) |
Clusiaceae | Garcinia cowa Roxb. ex Choisy | Cha moung ชะมวง | – | Wounds, ulcers, dysentery | Antioxidant, anti-inflammatory, leishmanicidal, antiprotozoal | Santo et al. (2020) |
Garcinia schomburgkiana Pierre | Ma dan มะดัน |
– | – | Anti-inflammatory, antibacterial, antioxidant, antitumor, antifungal, anti-HIV | Do et al. (2020) | |
Cucurbitaceae | Coccinia grandis (L.) Voigt | Tum lueng ตำลึง |
Leaves | Diabetics, skin diseases, jaundice, biliary disorders, coughs, spleen disorders, respiratory problems, mucus, leprosy, acne, diabetes, mucus in stool, goiter, antidote to poison, scabies, hypertension, abscess, lack of appetite, vomiting, dysentery, burns | Antioxidant, antimicrobial, cytotoxic, antimutagenic, antiulcer, hepatoprotective, expactorants, analgesic, anthelmintic, antidibetic, mast cell-stabilizing, anti-anaphylactic, antihistaminic, anti-inflammatory | Laboni et al. (2017) |
Cucurbita moschata Duchesne | Fak Thong ฟักทอง |
Seeds pulp peel |
Parasitic diseases caused by worms Reduced blood glucose and increased plasma insulin Hepatic disorders, peptic ulcer, gastrointestinal bleeding, wounds, burn |
Chemopreventive agent, antimicrobial, antihyperglycemic Antimicrobial, antidiabetic, cardioprotective, hypoglycaemic, antioxidative, anticancer, immunomodulatory, neuroprotective, anti-inflammatory Antioxidant, antibacterial |
Shaban & Sahu (2017), Salehi et al. (2019a), Kulczynski & Gramza-Michałowska (2019), Bahramsoltani et al. (2017) |
|
Cucurbitaceae | Momordica charantia L. | Mara มะระ |
Fruit | Hyperglycemia, oxidative stress, cancer, colitis | Antiulcer, anthelmintic, antidiabetic, anti-inflammatory, antimicrobial, antihyperglycemic, anticancer | Villarreal-La Torre et al. (2020), Ünal et al. (2020) |
Lagenaria siceraria (Molina) Standl. | Nam Tao น้ำเต้า |
Fruit | Rheumatism, insomnia, diuretic, urinary disorders, excessive thirst, emetic, sedative, purgative, cooling, diuretic, liver disorder, pectora | Antioxidant, laxative, cardioprotective, diuretic, hepatoprotective, hypolipidemic, central nervous system stimulant, anthelmintic, antihypertensive, immunosuppressive analgesic, adaptogen | Tyagi ,Sharma & Shrivastava (2017) | |
Luffa acutangular (L.) Roxb. | Bob ream บวบเหลี่ยม |
Fruit | Jaundice, swollen hemorrhoids, headache | Hepatoprotective, diabetic, hyperlipidemic, CNS depressant, ulcer, cancer, immunomodulatory, antibacterial | Shendge & Belemkar (2018), Panicker (2020) | |
Dilleniaceae | Dillenia indica L. | Ma tad มะตาด |
Arial part fruit |
Abdominal and joint pain, cough, diarrhoea, fever, tumours, diabetes, toning up the nervous system, removing fatigue Skin inflammation, kidney diseases |
Anti-inflammatory, antimicrobial, antidiabetic, hypolipidemic, antidiarrhoeal Anti-leukemic, anticancer antidiarrheal, antioxidant, CNS depressant, anti-inflammatory |
Kviecinski et al. (2017), Sen, Chakraborty & Kalita (2018) |
Euphorbiaceae | Phyllanthus emblica L. | Ma kham pom มะขามป้อม |
Fruit | Sore throat, cough, dry mouth, diarrhoea, jaundice, inflammation, diabetes mellitus, constipation, asthma | Immunosuppressive, antioxidant and anti-inflammatory, anti-microbial, hepatoprotective | Jantan et al. (2019), Li et al. (2020) |
Fabaceae | Acacia pennata (L.) Willd. | Cha om ชะอม |
Leaves bark root bark |
Body aches, headaches, fevers, helping digestion for infants Asthma and bronchitis Stomach pain, bronchitis, cholera, asthma |
Antinociceptive, anti-inflammatory, antifungal, DNA protection for drug abuse harmful effects, anti-flatulent, anti-parasitic | Aye et al. (2019), El-Taher et al. (2021) |
Clitoria ternatea L. | Anchan อัญชัน |
Various tissue | Enhance cognitive functions, alleviate symptoms of numerous ailments including fever, inflammation, pain, diabetes | Nootropic, anti-convulsant, anti-depressant, anti-anxiety, anti-stress, antioxidant, anti-inflammatory, anti-hyperlipidemic, anti-diabetic, analgesic, cytotoxicity, platelet aggregation inhibitory, hepatoprotective activities | Gollen, Mehla & Gupta (2018), Oguis et al. (2019) | |
Neptunia prostrata (Lam.) Baill. | Phak kra ched ผักกระเฉด |
Leaves | Astringent, sweet, refrigerant, diuretic, antidiarrheal, anti-helmintic, anodyne, dysentery, intestinal infection, fever, earache, poisoning, constipation, gastritis | Antioxidant, α-glucosidase inhibitors, anti-tumor, antibacterial, and α-glucosidase inhibitory, anti-inflammatory, antiulcer, anticancer | Sagolshemcha & Singh (2017), Lee et al. (2019) | |
Leucaena leucocephala (Lam.) de Wit | Kra tin กระถิน |
Leaves | Stomachache, contraceptive, abortifacient agent | Antimicrobial, anticancer, anti-inflammatory, anti-asthma, diuretic, antiarthritic, antifouling, anti-retroviral, anti-diabetic, anti-scabies, antiprotozoal, chemopreventive, immunostimulant, lipoxygenase inhibitor | Zayed, Sallam & Shetta (2018), Zayed, Wu & Sallam (2019) | |
Fabaceae | Parkia speciosa Hassk. | Sataw สะตอ |
Seeds and other | Loss of appetite, kidney disorder, diabetes, cardiovascular diseases, headache, severe cough, bronchitis | Anti-hypertensive, antioxidative, anti-inflammatory, anticancer, antimicrobial, antinociceptive | Chhikara et al. (2018), Saleh et al. (2021) |
Sesbania grandiflora (L.) Pers. | Dok Kae ดอกแค |
Flower leaves |
Astringent, fever, catarrh relief, nyctalopia eyes treatment, headache Thrombosis, diarrhea, inflammatory diseases, bronchitis, cough, vomiting, wounds, ulcer, diarrhea, dysentery, catarrh, headache |
Anti-inflammatory, antipyretic, antimicrobial, hepatoprotective, anti-plaque, anti-tumor | Mohiuddin (2019), Aye et al. (2019) | |
Senna siamea (Lam.) H.S.Irwin & Barneby | Khilek ขี้เหล็ก |
Leaves | Pain, oedema, constipation, infectious diseases | Laxative, anti-inflammatory analgesic | Ntandou et al. (2018), Nas, Oyeyi & Ali (2018) | |
Tamarindus indica L. | Ma kham มะขาม |
Fruit | Inflammation, stomach pain, throat pain, rheumatism, wound healing, diarrhea, dysentery, parasitic, infestation, fever, malaria, respiratory, helminthes infections, constipation, cell cytotoxicity, gonorrhea, eye diseases, aphrodisiac | Anti-inflammatory, analgesic, antioxidant, hypolipidemic, anti-helminthic, antimicrobial, hepatoprotective, anti-asthmatic, weight-reducing | Komakech et al. (2019), Borquaye et al. (2020) | |
Gnetaceae | Gnetum gnemon L. | Phak lueng ผักเหลียง |
Leaves | Malarial related fever, enhance health and stimulate milk production in pregnant women | Antioxidant, antiplasmodial, antibacterial, tyrosinase inhibitory | Dutta et al. (2018), Le et al. (2020) |
Hypericaceae | Cratoxylum formosum (Jacq.) Benth. & Hook.f. ex Dyer | Phak tiu ผักติ้ว |
Leaves | Fevers, diarrhea, itch, ulcer, coughs, stomachache, food poisoning, internal bleeding | Antioxidant, antimicrobial, anti-inflammatory | Rodanant et al. (2017), Juanda et al. (2019) |
Lamiaceae | Mentha × cordifolia Opiz ex Fresen. | Saranae สะระแหน่ |
Leaves | – | Analgesic, antioxidant, insecticidal, antimicrobial, antispasmodic, antiplatelet, anti-inflammatory | Sevindik (2018) |
Ocimum sanctum L. | Kaphrao กระเพรา |
Leaves | Ulcers, skin and mouth infections, fever, coughs, respiratory disorders, heart diseases, enhance memory | Antioxidant, antimicrobial, anti-inflammatory, adaptogen, immunomodulator, antidiabetic, anti-fertility, hepatoprotective, cardioprotective | Kaur et al. (2020), Almatroodi et al. (2020) | |
Ocimum gratissimum L. | Yira ยี่หร่า |
Leaves | Inflammatory bowel diseases, diarrhea, fungal infections, fever, cold catarrh | Anti-colitis, anti-oxidative, anti-inflammatory, antibacterial, antimalarial | Alabi et al. (2018) | |
Ocimum × africanum Lour. | Maeng lak แมงลัก |
Leaves | Cold, fever, parasitic infestations, inflammation of joints, headaches, skin diseases, lowering blood glucose, dysentery, diarrhoea, reduce constipation, lipid peroxidation | Antiarthritic, anti-inflammatory, insecticidal, antimicrobial, antioxidant, anthelmintic, antidiabetic | Marrelli et al. (2020), Chetia et al. (2021) | |
Ocimum basilicum L. | Horapha โหระพา |
Leaves | Kidney disorders, earache, menstrual irregularities, arthritis, anorexia, colds treatment, malaria, fevers, coughs, flu, asthma, bronchitis, influenza, diarrhea | Anti-cancer, radioprotective, antimicrobial, anti-inflammatory, immunomodu-latory, anti-stress, antidiabetic, anti-pyretic, anti-arthritic, antioxidant, prophylactic agent in cardiovascular disease | Shahrajabian, Sun & Cheng (2020) | |
Lauraceae | Cinnamomum verum J.Presl | Ob chei อบเชย |
Stem bark | Prevention of nausea and vomiting, common cold, cardiovascular diseases, chronic gastrointestinal disorders, general stimulant, microbial infections, antiseptic | Antioxidant, antimutagenic, antidiabetic, anticancer, antimicrobial, anti-inflammatory | Schink et al. (2018), Parham et al. (2020) |
Meliaceae | Azadirachta indica A. Juss. var. siamensis Valeton | Sadao สะเดา |
Leaves | Cancer, hypertension, heart diseases, diabetes | antipyretic, fungicidal, antihistamine, antiseptic, anti-inflammatory, antioxidant, antimicrobial, anticancer, antidiabetic | Islas et al. (2020) |
Menispermaceae | Cissampelos pareira L. | Khruea ma noi เครือหมาน้อย |
Leaves, root | Ulcer, rheumatism, fever, asthma, cholera, diarrhoea, rabies, blood purifying, snakebite, malaria, pneumonia | Anti-inflammatory, anti-leukemic, antinociceptive, anti-arthritic, anthelmintic, curariform, cardioprotective, antioxidant, immunomodulatory, chemo-modulatory, antibacterial | Iram et al. (2017), Kumari et al. (2021) |
Tiliacora triandra Diels | Yanang ย่านาง |
Pyretic, bacterial infections, detoxification, immune modulator agent | Antioxidant, anti-inflammatory, hepatic glucose production inhibitory, anticancer, anti-pyretic, acetylcholinesterase inhibitory | Weerawatanakorn et al. (2018), Makinde et al. (2019), Pasachan et al. (2021) | ||
Moringaceae | Moringa oleifera Lam. | Ma rum มะรุม |
Leaves, seed | Skin infection, asthma, diabetes, diarrhea, arthritis, inflammation, cough, fever, headache, cardiovascular and gastrointestinal diseases | Antioxidant, anti-inflammatory, antiarthritic, antitumor, antimicrobial, hepatoprotective | Jaja-Chimedza et al. (2017), Xu, Chen & Guo (2019), Saleem, Saleem & Akhtar (2020) |
Musaceae | Musa × paradisiaca L. | Hua Plee หัวปลี |
Flower juice | Stimulate breastmilk (Thailand), bronchitis, constipation, ulcers, inflammation of eyes, nervous debilities | Antioxidant, anti-inflammatory, antimicrobial, anti-obesity, pancreatic lipase inhibition, antimalarial | Shubham et al. (2019) |
Myristicaceae | Myristica fragrans Houtt. | Luke Chan thet ลูกจันทน์เทศ |
Seeds | Stomach disorders, peptic ulcer, nausea, dyspepsia, gastrointestinal tract | Antibacterial, anti-inflammatory, antioxidant, anticancer, antiseptic, antiparasitic | Suthisamphat et al. (2020) |
Myrtaceae | Syzygium aromaticum (L.) Merr. & L.M.Perry | Kanplu กานพลู |
Flower | Vomiting, flatulence, nausea; liver, bowel, and stomach disorders; microbial infectious diseases, dentistry | Analgesic, antioxidant, anticancer, antiseptic, anti-depressant, antispasmodic, anti-inflammatory, antiviral, antifungal, and antibacterial | Batiha et al. (2020a) |
Syzygium cumini L. | Luke wa ลูกหว้า |
Fruit | Cardiometabolic disorders, gastric issues, diabetes, dysentery | Antidiabetic, antihyperglycemic, antihyperlipidemic, anti-inflammatory, cardioprotective, antioxidant | Abdin et al. (2020), Qamar et al. (2021) | |
Nymphaeaceae | Nymphaea pubescens Willd. | Bua sai บัวสาย |
Flower | Circulatory system syndrome | Anticancer, antioxidant, neuroprotective | Aimvijarn et al. (2018), Rivas-García et al. (2021) |
Pandanaceae | Pandanus amaryllifolius Roxb. | Bai tei ใบเตย |
Leaves | Energize body, reduce fever, flatulence, diabetes mellitus | Antidiabetic, antioxidant, xanthine oxidase inhibitory, | Shukor et al. (2018), Reshidan, Abd Muid & Mamikutty (2019) |
Pedaliaceae | Sesamum indicum L. | Nga งา |
Seeds | Pain, fever, inflammation, constipation, diuretic, healing burns and wounds | Anti-inflammatory, antiaging, anticancer, antidiabetes, antioxidant, anticancer, antinociceptive, hepatoprotective, antiarthritic antihypertensive, chemoprotective | Deme, Narasimhulu & Parthasarathy (2018), Wu et al. (2019), Afroz et al. (2019) |
Phyllanthaceae | Sauropus androgynus (L.) Merr. | Phak waan baan ผักหวานบ้าน | Leaves | Body weight reduction, postpartum recovery, enhance lactation in feeding mothers, breast milk production, cholecystosis, diorrhea, oral thrush, nasal ulcers, and yaws; erythrema, measles | Anti-inflammatory, antidiabetic, anti-obesity, lactation inducing activity, anti-obesity, antimicrobial, anticancer, analgesic, antipyretic, aphrodisiac, anti-cholesterol, wound healing | Arif & Shetty (2020), Fikri & Purnama (2020) |
Piperaceae | Piper nigrum L. | Phrik Thai พริกไทย | Seeds | Rheumatism, diabetes, muscular ache, diuretic, increase salivary secretion, promote digestion, cold, cough, germicidal, blood purifier | Anti-inflammatory, anticancer, antimicrobial, anti-larvicidal, pesticide, anti-Alzheimer’s, antidepressant, bioavailability enhancer, immunomodulatory, anti-allergic, antidiabetic | Joshi, Shrestha & Adhikari (2018), Stojanović-Radić et al. (2019), Tiwari, Mahadik & Gabhe (2020) |
Piper sarmentosum Roxb. | Chaplu ชะพลู |
Leaves | Headache, relieve muscle weakness and pain; toothache, fungoid dermatitis on feet, coughing asthma, pleurisy, hypertension | Antimicrobial, antioxidant, reduced blood sugar level, neuromuscular blocking activity, anti-plasmodial, reduced blood pressure, anti-atherosclerotic | Bactiar & Fahami (2019), Fauzy et al. (2019), Sundar et al. (2019) | |
Plantaginaceae | Limnophila aromatica (Lam.) Merr. | Phak khayang ผักแขยง |
Whole plant | Jaundice, fever, digestion system, vascular dysfunction | Anti-inflammatory, anti-tumor, antioxidant | Dai et al. (2015) |
Poaceae | Cymbopogon citratus (DC.) Stapf | Ta khrai ตะไคร้ |
Stalk, leaves | Mosquito repellent in Thailand, analgesic, antipyretic, diuretic | Anti-obesity, antibacterial, antifungal, antinociceptive, antioxidants, antidiarrheal, anti-inflammatory, anti-rheumatic, cardioprotective, restrain platelet composition, cure diabetes, gastrointestinal infections, anxiety, or depression, antimalarial, pneumonia | Oladeji et al. (2019) |
Polygonaceae | Persicaria odorata (Lour.) Soják | Phak paw ผักแพว |
Leaves | Treat flatulence, relieve constipation | Anti-inflammatory, antioxidant, anticancer, anti-hemolytic, antibacterial | Chansiw et al. (2018), Ridzuan & Wan Salleh (2019) |
Rutaceae | Citrus × aurantium L. | Som sa ส้มซ่า |
Blossoms | Cough, phlegm, headache, flatulence | Anti-inflammatory, sedative, anti-anxiety, antidepressant, antibacterial, antifungal, | Shen et al. (2017) |
Rutaceae | Citrus hystrix DC. | Makrut มะกรูด |
Leaves Fruit |
Teeth and gum for nourishing dental health Herbal shampoo, inflammatory aliments, fever, headache, bad breath, digestion, flu, sore throats |
Anti-inflammatory, neuroprotective, anticancer, antioxidant, antibacterial |
Kidarn et al. (2018) Anuchapreeda et al. (2020), Pattarachotanant & Tencomnao (2020) |
Citrus aurantifolia (Christm.) Swingle | Manao มะนาว |
Fruit | Relieve sore throat and moisten the throat in Thailand, hypertension | Anticancer, antimicrobial, antioxidant, antiulcer, anti-inflammatory, hypolipidemic, antityphoid, hepatoprotective, anti-obesity, cardiovascular, anti-cholinesterase | Jain, Arora & Popli (2020) | |
Zanthoxylum rhetsa DC. | Ma khwaen มะแขว่น |
Fruit, seeds Bark |
Toothache, dizzy, bloating, reduce muscle strain, cholera, asthma, bronchitis, heart troubles, piles, relief of hiccup, diarrhea, rheumatism Cardiac, respiratory diseases, tooth infection, stomach infection, rheumatism |
Adulticidal, larvicidal, pupicidal, oviposition deterrent, herbicidal, antimalarial, anti-tuberculosis, anti-inflammatory, antiseptic, anticholera Antibacterial, anti-inflammatory, analgesic, anticancer, thrombolytic, photoprotective |
Soonwera & Phasomkusolsil (2017), Duangyod et al. (2020), Maduka & Ikpa (2021) |
|
Solanaceae | Capsicum frutescens L. | Phrik khinu พริกขี้หนู |
Fruit | Arthritis, rheumatism, stomach aches, skin rashes, wound healing, stimulate appetite | Antibacterial, antifungal, insecticidal, anthelmintic, larvicidal, antioxidant, anti-inflammatory | Batiha et al. (2020b) |
Capsicum annuum L. | Phrik chifah พริกชี้ฟ้า |
Fruit | Analgesic and inflammatory | Antimicrobial, anti-inflammatory, cardiovascular, anti-obesity, immunosuppressant, memory enhancing, antidiabetic | ||
Solanaceae | Lycopersicon esculentum Mill. | Makhuea thet มะเขือเทศ | Fruit | – | Anti-inflammatory, antioxidant, anti-atherosclerotic, anti-obesity, antihypertensive, antiplatelet, and lipid lowering | Mozos et al. (2018) |
Solanum stramoniifolium Jacq. | Ma uek มะอึก |
Fruit Leaves, root |
- Thrush, cold, venereal diseases, inflammation, asthma, arthritis, liver problems, malaria, and cancer |
Antibacterial Antibacterial, antioxidant, anti-inflammatory, cytotoxicity |
Svobodova et al. (2017) | |
Solanum torvum Sw. | Makhuea puang มะเขือพวง |
Fruit Leaves |
Fever, cough, wounds, pain, liver troubles, tooth decay, reproductive problems, arterial hypertension, antidote - |
Antioxidant, anti-inflammatory, antimicrobial, antiulcer, cardioprotective, analgesic, nephro-protective Hepatoprotective, immunomodulatory |
Darkwah et al. (2020) Innih, Agu & Eze (2018) |
|
Zingiberaceae | Alpinia galanga L. | Kah ข่า |
Rhizome | Respiratory diseases, stomach disorders, diarrhea, rheumatism, inflammation, diabetes, neurological disorders | Antimicrobial, anti-inflammatory, antioxidant, anti-hepatotoxic, antidiabetic, immunomodulatory, anti-ulcer, antitumor, anti-allergic, anti-HIV | Khairullah et al. (2020) |
Boesenbergia rotunda (L.) Mansf. | Krachai กระชาย |
Rhizome | It is believed to promote a healthy immune system, alleviating many gastrointestinal disorders | Anti-inflammatory, antimicrobial, anticancer, antimutagenic, antiparasitic, antiulcer, antileukemia, hepatoprotective, anti-SARS-CoV-2 | Rosdianto et al. (2020), Kanjanasirirat et al. (2020), Mohan et al. (2020a) | |
Curcuma longa L. | Kamin ขมิ้น |
Rhizome | Body mask (Thai folk), stomach ulcers, skin diseases, chest pain, cough, diabetes, rheumatism | Antioxidant, anti-inflammatory, antimutagenic, antimicrobial, anticancer | Hewlings & Kalman (2017), Rahaman et al. (2021) | |
Zingiberaceae | Zingiber cassumunar Roxb. | Plai ไพล |
Rhizome | Relieve flatulence and diarrhea, combined with other herbs as an herbal ball to alleviate muscle and musculoskeletal pain, inflammation, bruise, sprain, and strain | Antimicrobial, anticancer, anti-inflammatory, neuroprotective, antioxidant, anti-aging, skin-whitening, analgesic, antipyretic | Chongmelaxme et al. (2017), Li et al. (2019), Han et al. (2021) |
Zingiber officinale Rosco | Khing ขิง |
Rhizome | Cold, headache, coughs, aphthous ulcers, nausea, colic, heart palpitations, stimulates appetite, digestion-stimulation, rheumatism | Anti-inflammatory, antiviral, radioprotective, antioxidant, anticancer, antidiabetic, nephroprotective, hepatoprotective, larvicidal, analgesic, immunomodulatory | Mutthuraj et al. (2020), Dissanayake, Waliwita & Liyanage (2020) |
An updated list of bioactivities of the selected plants
Inflammation is divided into two types: acute and chronic. Acute inflammation is a defense mechanism induced in response to harmful stimuli such as infections, injuries, and chemicals and is recognized by swelling, redness, fever, and pain. Chronic inflammation will occur if acute inflammation lingers for a long time, eventually leading to oxidative stress-mediated diseases, heart disease, diabetes, cancer, arthritis, and bowel diseases like ulcerative colitis (Marefati et al., 2021). Infectious diseases caused by microorganisms and pathogenic viruses can also induce cellular responses, activating signaling molecules such as NO and ROS that contribute to the inflammatory process by triggering the release of a cytokine storm that includes pro-inflammatory cytokines like TNF-α and interleukin (IL-1β, IL-6); this results in cell death (apoptosis) that can lead to acute respiratory distress or syndrome (ARDS), as seen after infection with SARS-CoV-2 (Donma & Donma, 2020). In this regard, we provide a recent backdated review to update the field on the discovery of many extracts and isolated compounds from plant species, with a specific focus on anti-inflammatory properties observed upon administration in study models and on antimicrobial effects demonstrated against antibiotic-resistant bacteria and clinically significant viruses.
Anti-inflammatory activity
Many researchers and scientists have attempted to demonstrate the potential of selected plants as bioactive anti-inflammatory agents; this activity is assessed by decreasing and inhibiting different mediators and pathways, and by microscopic changes. Among the selected species, a total of 49 species in 24 families have recently been investigated for their anti-inflammatory effects through in vitro and in vivo experimental studies (Table 3). Crude extracts, fractions, juice, and isolated compounds of Thai food plant ingredients have all demonstrated the potential to complement searches for anti-inflammatory drugs. For example, supplementation with water-soluble polysaccharide from Allium sativum (Apiaceae) can attenuate dextran sulfate sodium-induced colitis in mice (Shao et al., 2020). Daily oral supplementation with anthocyanin extract from Clitoria ternatea (Fabaceae) for 1 week effectively reduced carrageenan-induced paw edema in rats as compared with ibuprofen (Yanti et al., 2020). Similarly, administration of a polyphenol-rich extract from Occimum gratissimum (Apiaceae) promoted repair of colonic mucosa injuries in a dosage-dependent manner in experimental colitis rats (Alabi et al., 2018).
Family | Botanical name | Local name | Tested samples | Assay/Study model | Results and mechanisms | References |
---|---|---|---|---|---|---|
Amaryllidaceae | Allium ascalonicum | Hom daeng หอมแดง | Juice | Lipopolysaccharide (LPS)-stimulated on human vascular endothelial cells | Significantly attenuated the level of IL-6 released | Ounjaijean et al. (2018) |
Allium sativum | Kra thiam กระเทียม | Water-soluble polysaccharide extract | Dextran sulfate sodium (DSS)-induced colitis in mice | Reduce DSS-induced colitis by improving mucosal barriers, blocking proinflammatory cytokines IL-6, TNF-α, and IL-1β, and modulating gut microbiota in colitis mice | Shao et al. (2020) | |
Apiaceae | Apium graveolens | Khuen chai คื่นช่าย | Methanol root extract | Acetaminophen-induced hepato-toxicity (AAH) rats. | Lowered serum levels of AST, ALT, ALP, TNF-α, and IL-1β | Emad et al. (2020) |
Centella asiatica | Bua bok บัวบก |
Ethanolic raw extract | In vitro LPS-stimulated RAW 264.7 cells and in vivo Sprague Dawley rats | Suppressed the level of pro-inflammatory cytokine/mediators and oxidative stress and consistent to the LPS-induced neuroinflammation Sprague Dawley rats’ model. | Hafiz et al. (2020) | |
Coriandrum sativum | Phak chi ผักชี |
Concoction with Coscinium fenestratum (Gaertn.) Colebr. | Carrageenan-induced rat paw-edema | Potent in vivo anti-inflammatory activity, significant reduction of ROS, and NO production by rat peritoneal cells and lack of iNOS expression confirmed the low NO production | Kothalawala et al. (2020) | |
Cuminum cyminum | Yira ยี่หร่า |
Isolated atypical nitrogen-containing flavonoid | LPS-stimulated RAW 264.7 cells | Exhibited inhibitory effect on nitride oxide, with IC50 of 5.25 μM | Kang et al. (2019) | |
Eryngium foetidum | Phak chi farung ผักชีฝรั่ง |
Hydro-methanolic extract | Heat-induced denaturation of protein and red blood cell (RBC) membrane stabilization | Inhibited heat induced protein denaturation and RBC membrane stabilization at different concentrations | Prabha, Athoibi & Dsouza (2019) | |
Basellaceae | Basella alba | Phak plung ผักปลัง | Aqueous leaf extract | Streptozotocin-induced diabetic rats | Stimulates the recovery of beta-islet morphology by modulating the peripheral production of inflammatory cytokines. | Arokoyo et al. (2018) |
Caricaceae | Carica papaya | Malako มะละกอ |
Freeze-dried leaf juice | AG129 mice infected with DEN-2 dengue virus | The inflammatory cytokine genes: CCL6/MRP-1, CCL8/MCP-2, CCL12/MCP-5, CCL17/TARC, IL1R1, IL1RN/IL1Ra, NAMPT/PBEF1 and PF4/CXCL4 were downregulated. | Norahmad et al. (2019) |
Cucurbitaceae | Coccinia grandis | Tum lueng ตำลึง |
Methanolic leaf extract | In vitro scratch wound healing of human keratinocyte and fibroblast | Increased the wound healing process from its antioxidant capacity that acted as a proton donor to neutralize reactive oxygen species and protected the human fibroblasts and keratinocytes from hydrogen peroxide-induced oxidative stress by increasing cell survival rate. | Namchaiw et al. (2021) |
Cucurbita moschata | Fak Thong ฟักทอง |
Tendrils extract Oleic acid ester of hydroxy oleic acid |
NLRP3 inflammasome activation in murine macrophages and human trophoblast cell LPS-stimulated dendritic cells |
Attenuated NLRP3 inflammasome activation and suppressed IL-1β secretion dose-dependently, without affecting IL-6 secretion. Moreover, it inhibited NLRP3-dependent pyroptosis in LPS-primed bone marrow-derived macrophages and significantly inhibited IL-1β secretion and pyroptotic cell death in human trophoblast cells. Reduced inflammation in adipose tissue by inhibiting the expression of cytokines IL-12, IL-1β, and TNF-α. |
Park et al. (2020), Dong et al. (2021) |
|
Momordica charantia | Mara มะระ |
Crude extract | 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis in rat | Showed protective anti-inflammatory effect | Ünal et al. (2020) | |
Luffa acutangular | Bob ream บวบเหลี่ยม |
Ethanolic fruit extract | Carrageenan-induced paw edema in Wistar albino rats | Exhibited moderate anti-inflammatory activity | Palash et al. (2017) | |
Dilleniaceae | Dillenia indica | Ma tad มะตาด |
Ethyl acetate fruit extract | Ultraviolet radiation-induced psoriasis-like wounds in rats | Healing effect within 16 days after wound induction which betulinic acid may be an active constituent | Kviecinski et al. (2017) |
Euphorbiaceae | Phyllanthus emblica | Ma kham pom มะขามป้อม |
Ethanolic fruit extract | LPS-induced RAW 264.7 cells | Exhibited antioxidant activity and decreased releasing of pro-inflammatory mediators | Li et al. (2020) |
Fabaceae | Clitoria ternatea | Anchan อัญชัน |
Anthocyanin extract | Carrageenan-induced rat paw edema | Protective activity via down-regulating genes of phosphoinositide 3-kinase signaling pathway | Yanti et al. (2020) |
Leucaena leucocephala | Kra tin กระถิน |
Leaf extract | Oxidized low density lipoprotein (oxLDL) and glucose-induce oxidative stress in human umbilical vein | Reduced oxidative stress condition in impaired fasting blood glucose patients that induce vascular endothelial dysfunction in diabetic and hyperlipidemia | Chatchanayuenyong, Sujayanont & Vuttivirojana (2018) | |
Parkia speciosa | Sataw สะตอ |
Ethyl acetate fraction of empty pod extract | Tumor necrosis factor-α (TNF-α)-induced inflammation human umbilical vein endothelial cells and H9c2 cardiomyocytes | Exhibited anti-inflammatory properties by modulating the NFκB and p38 MAPK pathways |
Sevindik (2018), Gui et al. (2019) |
|
Sesbania grandiflora | Dok Kae ดอกแค |
Leaf methanolic extract | Carrageenan-induced and formalin-induced rat paw edema | Inhibited formalin and carrageenan induced paw edema in 1–2 h of induction | Karale et al. (2018) | |
Senna siamea | Khilek ขี้เหล็ก |
Aqueous leaf extract | Carrageenan-induced rat paw edema and granuloma cotton pellet | Significant inhibition activity against acute and chronic inflammation. Moreover, the extract also significantly decreases the latency of the first fecal excretion increased the fecal excretion rate for laxative effects. | Ntandou et al. (2018) | |
Tamarindus indica | Ma kham มะขาม |
Fruit pulp extract Root and stem bark extracts |
LPS stimulated RAW 264.7 macrophages Carrageenan-induced paw edema in chicks |
Inhibit the production of nitric oxide and the iNOS gene expression Exhibited dose-dependent reduction of inflammation |
Leya & Anitha (2019) Borquaye et al. (2020) |
|
Gnetaceae | Gnetum gnemon | Phak lueng ผักเหลียง |
Seed extract | In vivo C57BL/6J mice fed with high-fat diet with 1% extract added | Induces brown adipose tissue (BAT) thermogenesis and reduces obesity-associated adipose tissue inflammation, hepatic steatosis, and insulin resistance | Yoneshiro et al. (2018) |
Hypericaceae | Cratoxylum formosum | Phak tiu ผักติ้ว |
Isolated lupeol Leaves crude extract |
LPS-stimulated phorbol-12-myristate-13-acetate (PMA)-stimulated-monocytes L-arginine methyl ester hydrochloride treated rats |
Inhibited the expression of TNF-α. Significantly alleviated left ventricular hypertrophy associated with reducing oxidative stress markers |
Rodanant et al. (2017), Potue et al. (2020) |
Lamiaceae | Ocimum gratissimum | Yira ยี่หร่า |
Polyphenol-rich extract | DSS-induced rat colitis | Showed potential to repair colonic mucosa injury in experimental colitis by regulating pro-inflammatory cytokines production and oxidative stress | Alabi et al. (2018) |
Ocimum basilicum | Horapha โหระพา |
Leaf extracts | Co-culture of 3T3-L1 Adipocytes and RAW264.7 Macrophages | Anti-inflammatory effect against adipocyte-induced inflammation, possibly through suppression of inflammatory signaling Tnfrsf9 expression (a member of the TNF super-family) as same as reduced expression of inflammatory cytokine mRNA on a co-culture | Takeuchi et al. (2020) | |
Lauraceae | Cinnamomum verum | Ob chei อบเชย |
Bark extract, p-cymene, trans-cinnamal-dehyde |
LPS-stimulated THP-1 monocyte-macrophage cell line | Mitigated the phosphorylation of Akt and IκBα. Moreover, trans-cinnamaldehyde and p-cymene significantly reduced the LPS-dependent IL-8 secretion in THP-1 monocytes. | Schink et al. (2018) |
Meliaceae | Azadirachta indica | Sadao สะเดา |
Leaf extract | Cigarette smoke and LPS-induced pulmonary inflammation in lungs mice | Decreased the production of ROS and the activity of neutrophil elastase in bronchoalveolar lavage fluid, blocking proinflammatory cytokines and the activation of extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK), and other pathways | Lee et al. (2017a) |
Menispermaceae | Cissampelos pareira | Khruea ma noi เครือหมาน้อย |
Pectin | LPS-stimulated RAW264.7 macrophages | DPPH and NO scavenging, NO production is inversely correlated to pectin concentration | Wisidsri & Thungmungmee (2019) |
Tiliacora triandra | Yanang ย่านาง |
Lyophilized leaf juice | LPS-stimulated RAW264.7 macrophages | Down-regulated the induction of inflammatory iNOS and COX-2 proteins | Weerawatanakorn et al. (2018) | |
Moringaceae | Moringa oleifera | Ma rum มะรุม |
Leaf extract | Wistar rats by formaldehyde induced arthritis | Significant antioxidant and anti-arthritic potential by in vitro anti-inflammatory assays such as protein denaturation, membrane stabilization and anti-proteinase activities | Saleem, Saleem & Akhtar (2020) |
Myristicaceae | Myristica fragrans | Luke Chan thet ลูกจันทน์เทศ |
Ethanolic aril extract | LPS-induced RAW264.7 cell line | Inhibited NO release and has cytotoxic activity against gastric cancer cell lines (Kato III) | Suthisamphat et al. (2020) |
Myrtaceae | Syzygium aromaticum | Kanplu กานพลู |
Formulated essential oil in absorption base ointment with added oleic and propylene glycol | Croton oil-induced inflammatory mice | Treatment showed less COX-2 expression, number of inflammatory cells, and epidermal thickness | Sugihartini et al. (2019) |
Myrtaceae | Syzygium cumini | Luke wa ลูกหว้า |
Isolated malvidin 3,5-diglucoside | LPS-induced RAW264.7 macrophages | Inhibited NO release and pro-inflammatory mediators like mouse IL-6, IL-1β) and TNF-α | Abdin et al. (2020) |
Pandanaceae | Pandanus amaryllifolius | Bai tei ใบเตย |
Leaf aqueous extract | Fructose-induced metabolic syndrome rat | Improved obesity parameters with neutral effects on inflammatory biomarkers | Reshidan, Abd Muid & Mamikutty (2019) |
Pedaliaceae | Sesamum indicum | Nga งา |
Methoxy phenol compounds in aqueous extract of sesame oil | LPS-induced monocyte-derived macrophages and RAW 264.7 cells | Attenuates inflammatory cytokines | Deme, Narasimhulu & Parthasarathy (2018) |
Phyllanthaceae | Sauropus androgynus | Phak waan baan ผักหวานบ้าน | Leaf patch | Carrageenan-induced rats | At 400 mg/kg showed healing activity after patch application. | Desnita et al. (2018) |
Piperaceae | Piper nigrum | Phrik Thai พริกไทย | Green pepper ethanolic extract | LPS-induced RAW 264.7 cells | Significantly suppressed nitrite production and inducible NO synthase expression without being cytotoxic. It also suppressed the LPS-induced phosphorylation of mitogen-activated protein kinases. | Kim et al. (2020) |
Piper sarmentosum | Chaplu ชะพลู |
Aqueous leaf extract | TNF-α-treated human umbilical vein endothelial cells | Promotes endothelial NO production by stimulating DDAH activity and reducing asymmetric dimethylarginine (ADMA) level, an endogenous inhibitor of endothelial nitric oxide synthase | Sundar et al. (2019) | |
Rutaceae | Citrus × aurantium | Som sa ส้มซ่า |
Essential oils from the flower | LPS-induced RAW 264.7 cells | Significant anti-inflammatory activities by inhibiting production of NO, IL6, TNF-α, IL-1β and decreased COX-2 gene and protein expression levels, inhibited NF-κB | Shen et al. (2017) |
Citrus hystrix | Makrut มะกรูด |
Isolated furanocoumarins | LPS-interferon gamma-induced cell lines | Inhibited NO and iNOS in RAW264.7 cells and COX-2 production in HT-29 and HCT116 cells. | Kidarn et al. (2018) | |
Rutaceae | Citrus hystrix | Makrut มะกรูด |
Isolated terpenoid agrostophillinol Ethanolic leaf extract, lupeol |
Leukemic and RAW264.7 cells LPS-stimulated and NLRP3 adenosine triphosphate-induced macrophages |
Showed anti-leukemic and anti-inflammatory by significantly inhibited IL-6 secretion Significantly reduced the release of pro-inflammatory cytokines and suppressed the expression of both inflammasome genes and NF-κB proteins and NLRP3 signaling pathways |
Anuchapreeda et al. (2020), Buakaew et al. (2021) |
Citrus aurantifolia | Manao มะนาว |
Peel extract | Balb/c mice infected by Salmonella typhi | Decreased serum level of IL6 | Kasim et al. (2020) | |
Zanthoxylum rhetsa | Ma khwaen มะแขว่น |
Pericarp and seed essential oil extracts | LPS-induced RAW 264.7 macrophages | Showed inhibition of inflammatory mediators (NO, TNF-α, and PGE2) | Imphat et al. (2021) | |
Solanaceae | Solanum stramoniifolium | Ma uek มะอึก |
Root extract | LPS-induced RAW 264.7 macrophages | Inhibited NO production | Svobodova et al. (2017) |
Solanum torvum | Makhuea puang มะเขือพวง |
Isolated spirostanol derivatives | RBL-2H3 basophilic leukemia cell line | Showed anti-metastatic and anti-inflammatory effects against interleukin-4 (IL-4) release in inflammation-associated tumors | Lee et al. (2017b) | |
Zingiberaceae | Boesenbergia rotunda | Krachai กระชาย |
Isolated boesenbergin A | Ethanol-induced gastric ulcer in vivo | Reduced ulcerated and haemorrhagic areas by boosting gastric mucus production, suppressed inflammatory mediators (TNF-α and IL-6 cytokines) and modulated the oxidative stress response | Mohan et al. (2020a) |
Curcuma longa | Kamin ขมิ้น |
Co-treatment with Allium hookeri extract | Carrageenan-induced air pouch and LPS-induced RAW 264.7 cells | Ratio as 3:7 suppressed inflammatory cytokines and inhibited NF-κB/COX-2/iNOS pathway | Lee et al. (2020) | |
Zingiberaceae | Zingiber cassumunar | Plai ไพล |
Gel containing Plai oil–encapsulated niosomes (E)-3-(3,4-dimethoxyphenyl)-2-propenal; 1-feruloyloxy cinnamic acid; (1E,4E,6E)-1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one; bisdemethoxycurcumin; and curcumin |
Inflamed subcutaneous Wistar rat skin by therapeutic ultrasound LPS-induced mouse macrophages cell (RAW264.7) |
Decreased skin temperature and blood flow to the lowest level compared to the application of neurofen drug Five active compounds showed anti-inflammatory potentials with NO generation inhibition |
Leelarungrayub, Manorsoi & Manorsoi (2017) Li et al. (2019) |
Zingiber officinale | Khing ขิง |
Essential oil extract | Administering with fresh and dry ginger essential oil (external apply) on Arthritis patients | Decreased rheumatoid arthritis factor and level of c-reactive protein produced | Mutthuraj et al. (2020) |
Additionally, plant parts besides the edible ones have shown anti-inflammatory properties, such as with an ethyl acetate fraction of empty pod extract of Parkia speciosa (Fabaceae) (Sevindik, 2018; Gui et al., 2019), root and stem bark extract of Tamarindus indica (Fabaceae) (Borquaye et al., 2020), and flower essential oil of Citrus aurantium (Rutaceae) (Shen et al., 2017). Some bioactive candidates for anti-inflammatory effect have lately been identified, for example: an atypical nitrogen-containing flavonoids from Cuminum cyminum (Apiaceae) (Kang et al., 2019); oleic acid ester of hydroxy oleic acid from Cucurbita moschata (Cucurbitaceae) (Dong et al., 2021); lupeol from Cratoxylum formosum (Hypericaceae) (Rodanant et al., 2017) and Citrus hystrix (Rutaceae) (Buakaew et al., 2021); the terpenoid agrostophillinol (Anuchapreeda et al., 2020) and furanocoumarins (Kidarn et al., 2018) also from Citrus hystrix (Rutaceae); p-cymene and trans-cinnamaldehyde from Cinnamomum verum (Lauraceae) (Schink et al., 2018); pectin from Cissampelos pareira (Menispermaceae) (Wisidsri & Thungmungmee, 2019); malvidin 3,5-diglucoside from Syzygium cumini (Myrtaceae) (Abdin et al., 2020); methoxy phenol compounds from Sesamum indicum (Pedaliaceae) (Deme, Narasimhulu & Parthasarathy, 2018); spirostanol derivatives from Solanum torvum (Solanaceae) (Lee et al., 2017b); boesenbergin A from Boesenbergia rotunda (Zingiberaceae) (Mohan et al., 2020a), and the compounds (E)-3-(3,4-dimethoxyphenyl)-2-propenal, 1-feruloyloxy cinnamic acid, (1E,4E,6E)-1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one, bisdemethoxycurcumin, and curcumin from Z. cassumunar (Li et al., 2019), also of the family Zingiberaceae.
Reports of bioactivity have also been published for gel, ointment, and patch formulations, and for co-treatment with selected plants (Table 3). In one case, a concoction of Coriandrum sativum (Apiaceae) with Coscinium fenestratum showed potent in vivo anti-inflammatory activity (Kothalawala et al., 2020). Anti-inflammatory effects with potential in product development have also been exhibited by essential oil from Syzygium aromaticum (Myrtaceae) formulated in an absorption base ointment with added oleic and propylene glycol (Sugihartini et al., 2019), a leaf patch from Sauropus androgynus (Phyllanthaceae) (Desnita et al., 2018), and a gel containing encapsulated niosomes of Plai oil (Z. cassumunar, Zingiberaceae) (Leelarungrayub, Manorsoi & Manorsoi, 2017). Finally, co-treatment using Curcuma longa (Zingiberaceae) and Allium hookeri extracts at a ratio of 3:7 showed optimal anti-inflammatory properties, indicating a synergistic plant-plant combination effect (Lee et al., 2020).
However, there still remains a need to establish a direct link between a plant extract and its putative bioactive compounds, for example flavonoids and essential oils, to further elucidate the anti-inflammatory role and help design clinical research and address the current insufficient body of evidence. This will allow developing a better understanding and implementation that might promote health maintenance and prevent numerous health conditions and diseases related to the inflammatory response.
Antibacterial
Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae have been listed as antibiotic-resistant bacteria by the World Health Organization (WHO) since 2017. Of those, P. aeruginosa (carbapenem-resistant) and Enterobacteriaceae like K. pneumoniae and E. coli (carbapenem-resistant) can produce extended-spectrum beta-lactamases (ESBLs) to interfere with beta-lactam antibiotics, and are accordingly ranked as of the utmost priority, followed by S. aureus (methicillin-resistant and vancomycin-intermediate and -resistant) (Magryś, Olender & Tchórzewska, 2021). Moreover, as noted in a previous systematic review article, these bacteria have been ranked as the top four targeted pathogenic bacteria for a decade, indicating the ongoing need to combat their antibiotic-resistant strains (Chassagne et al., 2021). The authors also pointed out in that review that among the 15 most represented plant families, those most reported as having antibacterial activities are Lamiaceae, Fabaceae, and Asteraceae.
Here, we provide recent scientific articles on plants used in Thai food, covering a total of 51 plant species in 25 families that have been reported as having antibacterial effects against the abovementioned human pathogenic bacteria (Table 4). In short, several studies have demonstrated broad antibacterial activity against both Gram-positive and Gram-negative bacteria in plant genera belonging to the families of Amaranthaceae (Nayak et al., 2018; Bilal & Hossain, 2019), Amaryllidaceae (Anyaegbunam et al., 2019; Enejiyon et al., 2020; Magryś, Olender & Tchórzewska, 2021), Apiaceae (Salehi et al., 2019b; Ali & Malik, 2020; Aboody, 2021), Cleomaceae (Ganesh, Muthusamy & Jaganathan, 2018; Kanimathi et al., 2019), Fabaceae (Anantaworasakul et al., 2017; Ghasemzadeh et al., 2018; Nas, Oyeyi & Ali, 2018; Noviany et al., 2020; Muhialdin, Abdul Rani & Hussin, 2020), Lamiaceae (Mittal, Kumar & Chahal, 2018; Jesuwenu & Michael, 2017; Melo et al., 2019), Menispermaceae (Uthpala & Raveesha, 2019), Myristicaceae (Dzotam et al., 2018; Kiarsi et al., 2020), Myrtaceae (Moemenbellah-Fard et al., 2020), Poaceae (Subramaniam, Yew & Sivasamugham, 2020), Rutaceae (Sreepian et al., 2019; Srifuengfung et al., 2020), Solanaceae (Obiang et al., 2019), and Zingiberaceae (Beristain-Bauza et al., 2019).
Family | Botanical name | Local name | S. aureus | E. coli | P. aeruginosa | K. pneumoniae | References |
---|---|---|---|---|---|---|---|
Amaranthaceae | Suaeda maritima | Cha kram ชะคราม |
+ | + | + | + | Nayak et al. (2018), Bilal & Hossain (2019) |
Amaryllidaceae | Allium cepa | Hom yai หอมใหญ่ |
+ | + | + | + | Anyaegbunam et al. (2019), Enejiyon et al. (2020) |
Allium sativum | Kra thiam กระเทียม |
+ | + | + | + | Magryś, Olender & Tchórzewska (2021) | |
Apiaceae | Apium graveolens | Khuen chai คื่นช่าย |
+ | NA | + | + | Salehi et al. (2019b), Aboody (2021) |
Centella asiatica | Bua bok บัวบก |
+ | + | + | + | Soyingbe, Mongalo & Makhafola (2018) | |
Coriandrum sativum | Phak chi ผักชี |
+ | + | + | NA | Ali & Malik (2020) | |
Cuminum cyminum | Yira ยี่หร่า |
+ | + | NA | NA | Wongkattiya et al. (2019) | |
Eryngium foetidum | Phak chi farung ผักชีฝรั่ง | + | + | NA | NA | Dalukdeniya & Rathnayaka (2017) | |
Basellaceae | Basella alba | Phak plung ผักปลัง |
+ | + | NA | NA | Deka et al. (2017) |
Caricaceae | Carica papaya | Malako มะละกอ |
+ | + | + | NA | Ukaegbu-Obi, Anyaegbunam & Enya (2018) |
Cleomaceae | Cleome gynandra | Phak Sian ผักเสี้ยน |
+ | + | + | + | Ganesh, Muthusamy & Jaganathan (2018), Kanimathi et al. (2019) |
Cucurbitaceae | Coccinia grandis | Tum lueng ตำลึง |
+ | + | + | NA | Laboni et al. (2017) |
Cucurbita moschata | Fak Thong ฟักทอง |
– | NA | + | + | Dash & Ghosh (2018) | |
Momordica charantia | Mara มะระ |
+ | + | + | NA | Villarreal-La Torre et al. (2020) | |
Lagenaria siceraria | Nam Tao น้ำเต้า |
– | NA | + | + | Ahmed & Ashiq (2018), Dash & Ghosh (2018) | |
Dilleniaceae | Dillenia indica | Ma tad มะตาด |
+ | + | NA | NA | Meeprathom, Jongrattanavit & Kooprasertying (2018) |
Euphorbiaceae | Phyllanthus emblica | Ma kham pom มะขามป้อม | + | + | NA | + | Ashalatha, Hemalatha & Raveesha (2019) |
Fabaceae | Clitoria ternatea | Anchan อัญชัน |
+ | + | NA | NA | Mahmad et al. (2018) |
Neptunia prostrata | Phak kra ched ผักกระเฉด |
+ | NA | NA | NA | Chakraverty et al. (2019) | |
Leucaena leucocephala | Kra tin กระถิน |
+ | NA | NA | + | Umaru, Samling & Umaru (2018) | |
Parkia speciosa | Sataw สะตอ |
+ | + | + | NA | Ghasemzadeh et al. (2018), Muhialdin, Abdul Rani & Hussin (2020) | |
Sesbania grandiflora | Dok Kae ดอกแค |
+ | + | + | + | Anantaworasakul et al. (2017), Noviany et al. (2020) | |
Senna siamea | Khilek ขี้เหล็ก |
NA | + | + | + | Nas, Oyeyi & Ali (2018) | |
Tamarindus indica | Ma kham มะขาม |
+ | + | NA | NA | Adeniyi et al. (2017) | |
Gnetaceae | Gnetum gnemon | Phak lueng ผักเหลียง |
+ | + | + | NA | Parhusip et al. (2019), Dayoh & Rahayu (2021) |
Lamiaceae | Ocimum sanctum | Kaphrao กระเพรา |
+ | NA | NA | + | Mittal, Kumar & Chahal (2018) |
Ocimum gratissimum | Yira ยี่หร่า |
+ | + | NA | + | Jesuwenu & Michael (2017), Melo et al. (2019) | |
Ocimum × africanum | Maeng lak แมงลัก |
+ | + | NA | NA | Chetia et al. (2021) | |
Ocimum basilicum | Horapha โหระพา |
NA | + | NA | NA | Juliet et al. (2019) | |
Lauraceae | Cinnamomum verum | Ob chei อบเชย |
+ | + | + | NA | Kwak, Kim & Kim (2017), Parham et al. (2020) |
Meliaceae | Azadirachta indica | Sadao สะเดา |
+ | + | + | NA | Maleki et al. (2018) |
Menispermaceae | Cissampelos pareira | Khruea ma noi เครือหมาน้อย |
+ | + | + | + | Uthpala & Raveesha (2019) |
Tiliacora triandra | Yanang ย่านาง |
+ | + | NA | NA | Makinde et al. (2019) | |
Moringaceae | Moringa oleifera | Ma rum มะรุม |
+ | + | + | + | Bancessi et al. (2020) |
Myristicaceae | Myristica fragrans | Luke Chan thet ลูกจันทน์เทศ |
+ | + | + | + | Dzotam et al. (2018), Kiarsi et al. (2020) |
Myrtaceae | Syzygium aromaticum | Kanplu กานพลู |
+ | + | + | + | Moemenbellah-Fard et al. (2020) |
Syzygium cumini | Luke wa ลูกหว้า |
+ | + | + | NA | Sharma et al. (2017) | |
Phyllanthaceae | Sauropus androgynus | Phak waan baan ผักหวานบ้าน | + | + | + | NA | Kuttinath, Haritha & Rammohan (2019) |
Piperaceae | Piper nigrum | Phrik Thai พริกไทย |
+ | + | NA | + | Hikal, 2018; Reshmi & Raj (2020) |
Piper sarmentosum | Chaplu ชะพลู |
+ | NA | + | + | Ibrahim & Nazir (2019) | |
Poaceae | Cymbopogon citratus | Ta khrai ตะไคร้ |
+ | + | + | + | Subramaniam, Yew & Sivasamugham (2020) |
Polygonaceae | Persicaria odorata | Phak paw ผักแพว |
+ | – | – | NA | Chansiw et al. (2018) |
Rutaceae | Citrus hystrix | Makrut มะกรูด |
+ | + | + | + | Sreepian et al. (2019), Srifuengfung et al. (2020) |
Citrus aurantifolia | Manao มะนาว |
NA | + | NA | + | Zage, Tajo & Ali (2018) | |
Solanaceae | Lycopersicon esculentum | Makhuea thet มะเขือเทศ |
+ | NA | NA | + | Shamshirgaran et al. (2020) |
Solanum stramoniifolium | Ma uek มะอึก |
NA | + | + | + | Svobodova et al. (2017) | |
Solanum torvum | Makhuea puang มะเขือพวง |
+ | + | + | + | Obiang et al. (2019) | |
Zingiberaceae | Boesenbergia rotunda | Krachai กระชาย |
+ | + | NA | NA | Atun, Handayani & Rakhmawati (2018) |
Curcuma longa | Kamin ขมิ้น |
+ | + | + | NA | Praditya et al. (2019) | |
Zingiber cassumunar | Plai ไพล |
+ | + | + | NA | Taechowisan, Suttichokthanakorn & Phutdhawong (2018) | |
Zingiber officinale | Khing ขิง |
+ | + | + | + | Beristain-Bauza et al. (2019) |
Note:
+, inhibited; −, not inhibited; NA, not analyzed.
When considering selected genera within a family screened for antibacterial activity, particularly prominent species include Centella asiatica of Apiaceae (Soyingbe, Mongalo & Makhafola, 2018), Coccinia grandis (Laboni et al., 2017), Momordica charantia (Villarreal-La Torre et al., 2020) of Cucurbitaceae, Sesbania grandiflora of Fabaceae (Anantaworasakul et al., 2017; Noviany et al., 2020), Cissampelos pareira of Menispermaceae (Uthpala & Raveesha, 2019), Solanum spp. of Solanaceae (Svobodova et al., 2017; Obiang et al., 2019), and Curcuma longa (Praditya et al., 2019) and Zingiber spp. of Zingiberaceae. Recent publication has rarely investigated all four targeted pathogenic bacteria in a single experimental design. Thus, the evidence is decisive only for the tested antibacterial actions of each plant species. However, some of the selected plant species have demonstrated broad antibacterial activity. For example, among eight bacteria strains tested, fresh Allium sativum (Amaryllidaceae) extract had the lowest MIC value of 6.25% (mg/ml) against S. aureus (MSSA and MRSA), E. coli (ATCC 25922 and MBL), and K. pneumoniae (ESBL) (Magryś, Olender & Tchórzewska, 2021). As another example, fruit extract of Solanum torvum (Solanaceae) showed potent antibacterial activity against multiple clinical bacterial isolates, with MIC values ranging from 1.25–5 μg/mL (Obiang et al., 2019).
In many cases, the antibacterial activity of a plant extract may be ascribed to predominant essential oils, such as in an essential oil extract of Ocimum gratissimum (Lamiaceae) that exhibited MIC values of 1,000 μg/mL against S. aureus and E. coli (Melo et al., 2019). Fruit peel oil and leaf oil of Citrus hystrix (Rutaceae) formulated as oral sprays have demonstrated antibacterial activity against respiratory pathogens, including S. aureus ATCC 29213 (Srifuengfung et al., 2020). Other classes of compounds also function as bioactive antibacterial agents, as demonstrated for the phenylbutanoid (E)-3-(3,4-dimethoxyphenyl)-4-[(E)-3,4-dimethoxystyryl] cyclohex-1-ene isolated from Z. cassumunar (Zingiberaceae), which showed high antibacterial activity against S. aureus and E. coli with MIC values of 16 μg/mL (Taechowisan, Suttichokthanakorn & Phutdhawong, 2018), while also having only weak cytotoxic activity. These findings support that many plant ingredients in Thai food can be taken as supplements for restoring health and can serve as powerful resources for developing antibiotic agents to treat serious and common infectious diseases.
Antiviral activities
Given the pandemic situation for the past few years, new and effective antiviral agents are needed for the development of vaccines and drugs. Currently available synthetic drugs may have adverse effects or cause drug resistance to nucleoside analogs via mutation (Mohan et al., 2020b). For these reasons, plant sources and phytomedicine have gained much interest in relation to antiviral drug discovery. Edible and medicinal plants are a powerful source of bioactive compounds and advantageous in terms of safety. Among the 69 plant species covered here, a few have been well-studied with regard to constituent phytochemicals and have demonstrated broad antiviral activities; these include Allium sativum (Amaryllidaceae) (Rouf et al., 2020) and Curcuma longa (Zingiberaceae) (Praditya et al., 2019; Jennings & Parks, 2020). Antioxidant and antimicrobial effects have also been reported for species including Syzygium aromaticum, Eryngium spp., Cinnamomum spp., Curcuma longa, and Z. officinale (Parham et al., 2020). In the current review, we give an update on 17 plant species (12 families) recently published for their antiviral activity against some human viruses (Table 5). In particular, several studies have demonstrated effectiveness of plant extracts and, in some cases, isolated compounds against important enveloped DNA and RNA viruses that cause human diseases such as influenza A, herpesvirus, Dengue virus, Zika virus, and Chikungunya virus, and against the non-enveloped RNA poliovirus. These viruses cause infectious diseases on scales ranging from individual infections and small local outbreaks to pandemics. As regards plant species, Moringa oleifera (Moringaceae) (Nasr-Eldin, Abdelhamid & Baraka, 2017; Ashraf et al., 2017; Adamu et al., 2020) and Piper nigrum (Piperaceae) (Priya & Kumari, 2017; Nag & Chowdhury, 2020) are of particular interest as they have shown a vaster range of antiviral activities. In the case of Piper nigrum, this might be an effect of the bioactive alkaloid piperine or derivatives, which are known for antiviral effects against HSV and the flu virus (Mohan et al., 2020b), while the activity of Moringa oleifera may be attributable to isothiocyanate-1, which possess anti-inflammatory properties, or to other constituents (Jaja-Chimedza et al., 2017). Moreover, comparing plant species in Table 5 with Table 1 reveals 14 antiviral plants that have exhibited anti-inflammatory properties, suggesting a synergism between immunomodulatory effects and the inhibition of viral invasion or replication.
Family | Botanical name | Local name | Activity | Dose (μg/mL) | References |
---|---|---|---|---|---|
Apiaceae | Centella asiatica | Bua bok บัวบก |
Water extract showed anti-herpes simplex virus (HSV1) Water extract showed anti-herpes simplex virus (HSV2) |
362.40 298.84 |
Garber, Barnard & Pickrell (2021) |
Coriandrum sativum | Phak chi ผักชี |
Aqueous extracts reduced the formation of HSV1 plaques | 350 | Fayyad, Ibrahim & Yaakob (2017) | |
Caricaceae | Carica papaya | Malako มะละกอ |
Fruit pulp extract showed inhibition against the Zika virus Lactic fermented pulp showed inhibition against the Zika virus Leaves extract treated adult dengue patients increased platelet counts compared to placebo group |
0.3 4 >1000 |
Haddad et al. (2020), Sathyapalan et al. (2020) |
Cucurbitaceae | Momordica charantia | Mara มะระ |
Ethanolic extract inhibited human herpes virus-3 (Varicella Zoster virus or HHV-3) Inhibition against the Zika virus |
125 507.2 |
Angamuthu et al. (2019), Vista et al. (2020) |
Fabaceae | Acacia pennata | Cha om ชะอม |
Inhibition against aquatic stages of the dengue virus vector: the 3rd instar larvae and pupae. |
>1000 | Thongwat, Ganranoo & Chokchaisiri (2017) |
Leucaena leucocephala | Kra tin กระถิน |
Inhibition against yellow fever virus (BeH111 strain) Inhibition against dengue 1 virus (Hawaii strain) |
>1000 >1000 |
Kaushik et al. (2018) | |
Tamarindus indica | Ma kham มะขาม |
Inhibition against Newcastle disease virus replication | >1000 | Okoh et al. (2017) | |
Lamiaceae | Ocimum sanctum | Kaphrao กระเพรา |
Crude extract showed highly significant in decreasing the H9N2 virus replication using in ovo model. | >1000 | Ghoke et al. (2018) |
Menispermaceae | Tiliacora triandra Diels | Yanang ย่านาง |
Ethanolic extract strongly inhibited porcine reproductive and respiratory syndrome virus infectivity in MARC-145 cells | >1000 | Arjin et al. (2020) |
Moringaceae | Moringa oleifera | Ma rum มะรุม |
Inhibitory activity against HSV1 and HSV2 Inhibitory activity against Influenza virus Inhibitory activity against Poliovirus |
200 0.78–100 >1000 |
Nasr-Eldin, Abdelhamid & Baraka (2017), Ashraf et al. (2017), Adamu et al. (2020) |
Myrtaceae | Syzygium aromaticum | Kanplu กานพลู |
Inhibition against Newcastle disease virus replication | – | Mehmood, Farooq & Youusaf (2020) |
Piperaceae | Piper nigrum | Phrik Thai พริกไทย | Inhibitory activity against Vesicular stomatitis Indiana virus Inhibitory activity against Human parainfluenza virus Inhibitory activity of Methyltransferase (PDB id 1L9K) of Dengue and VP35 Interferon Inhibitory Domain (PDB id 3FKE) of Ebola virus |
200 600 – |
Priya & Kumari (2017), Nag & Chowdhury (2020) |
Poaceae | Cymbopogon citratus | Ta khrai ตะไคร้ |
Inhibitory activity against dengue virus serotype 2 (DENV-2) | 20 | Rosmalena et al. (2019) |
Solanaceae | Capsicum annuum | Phrik chifah พริกชี้ฟ้า |
Inhibitory activity against HSV1 and HSV2 | 25 | Hafiz et al. (2017) |
Zingiberaceae | Boesenbergia rotunda | Krachai กระชาย |
Extract suppressed coronavirus SARS-CoV-2 infectivity Isolated compound cyclohexenyl chalcone derivative Panduatin A suppressed SARS-CoV-2 infectivity |
3.62 0.81 |
Kanjanasirirat et al. (2020) |
Curcuma longa | Kamin ขมิ้น |
Inhibitory activity against dengue virus serotype 2 (DENV-2) | 147 | Ichsyani et al. (2017) | |
Zingiber officinale | Khing ขิง |
Gingerenone A inhibited Janus Kinase 2 activity against influenza A virus Inhibitory activity against Chikungunya virus |
– 62.5 |
Wang et al. (2020), Kaushik et al. (2020) |
Remarkably, some plant species stand out based on their effectiveness at very low concentrations; these are Carica papaya (Caricaceae) (Haddad et al., 2020), Cissampelos pareira (Menispermaceae) (Ashraf et al., 2017), and B. rotunda (Zingiberaceae) (Kanjanasirirat et al., 2020), and the findings suggest sufficient specificity (extracts were used at concentrations of less than 10 µg/mL) that these might be good candidates for developing antiviral agents and merit further evaluation against a broader group of viruses. Particularly, B. rotunda extract and its isolated component panduratin A have promising antiviral activity against SARS-CoV-2 (COVID-19) (Kanjanasirirat et al., 2020). The authors found that infected Vero E6 cells were rapidly suppressed after treatment with extract or panduratin A, which had IC50 values of 3.62 μg/mL (CC50 = 28.06 μg/mL) and 0.81 μM (CC50 = 14.71 μM), respectively. At the pre-entry phase, panduratin A inhibited SARS-CoV-2 infection with IC50 of 5.30 μM (CC50 = 43.47 μM). However, we have only summarized recent investigations of antiviral activity. Many more plant species on the list might also have potential as sources of antiviral agents, just waiting for other researchers to discover them.
Conclusions
Plants used as ingredients in Thai food are typically also medicinal plants with applications proven long ago in folk medicine. This review describes the great extent of available information on edible and medicinal plants and isolated molecules from Thai food sources, which until now has existed as scattered pieces of information that have never been combined. The plant list includes diverse families with therapeutic importance supported by the various pharmacological activities, significant bioactive metabolites, and updated anti-inflammatory, antibacterial, and antiviral properties for which evidence has been collected in recent years. Based on the literature, plants used as ingredients in Thai food would be justified as elements of a healthy and functional diet and as sources of up-and-coming drug candidates with lesser toxicity. Many plant species have dual activity, demonstrating both anti-inflammatory and antimicrobial effects towards antibiotic-resistant bacteria and clinically significant viruses. In addition, more than one plant species is generally used for a single dish, as in traditional medicine practice. Hence, the effect of plant-plant combinations should be evaluated so as to enhance health restoration, therapeutic effects, and the development of supplementation and pharmaceutical-related products.
In Thailand, Andrographis paniculata (Burm. f.) Wall. ex Nees or Fah Talai Jone, a plant that has been used to treat and relieve common cold symptoms for years, has been included in The National List of Essential Drugs since 1999 and has become of renewed interest because of the COVID-19 pandemic around the globe. Encapsulated powder or extract of Andrographis paniculata with its major component, andrographolide, taken as a dose of 180 mg per day for five consecutive days, was recommended by the department of medicinal services for patients with mild symptoms (Mahajaroensiri et al., 2021). Concerning toxicity, a recent research article indicated that Andrographis paniculata extract and andrographolide respectively had no toxicity and a favorable toxicity profile in six representative human cell lines from the liver, kidney, intestine, lung, and brain. Both extract and andrographolide possess anti-SARS-CoV-2 activity and should be further investigated for their bioavailability and development for clinical applications as a monotherapy or in combination with other drugs (Sa-Ngiamsuntorn et al., 2021). In addition to that exemplar, this review emphasizes a promising plant list that will be of help in encouraging further investigation into mechanisms, synergy with antibiotics, formulations, physicochemical properties, bioavailability, and clinical research for the practical utilization of bioactive plant products. Moreover, the current review shall aid in the better selection of plant parts and species and promote their evaluability as food ingredients, functional foods, beverages, dietary supplements, and herbal medicines to preserve and increase vitality, slow aging, and promote well-being.