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Review

Essential Oils and Melatonin as Functional Ingredients in Dogs

by
Domingo Ruiz-Cano
1,
Ginés Sánchez-Carrasco
1,
Amina El-Mihyaoui
2 and
Marino B. Arnao
2,*
1
Alinatur Pet Food, S.L., Pol. Ind. Saprelorca, Lorca, 30817 Murcia, Spain
2
Department of Plant Biology (Plant Physiology), Faculty of Biology, University of Murcia, 30100 Murcia, Spain
*
Author to whom correspondence should be addressed.
Animals 2022, 12(16), 2089; https://doi.org/10.3390/ani12162089
Submission received: 4 July 2022 / Revised: 7 August 2022 / Accepted: 12 August 2022 / Published: 16 August 2022

Abstract

:

Simple Summary

Phytogenics are plant-based compounds with beneficial actions in feed technology and/or animal health. These so-called plant secondary metabolites are very diverse and with wide possible applications in humans and animals. Among them, essential oils (EOs) are the most used in feed for livestock and pets. Lately, melatonin has acquired new and interesting applications in dogs. Recent studies using EOs and/or melatonin in dog feeding and their involvement in health aspects are presented.

Abstract

The use of nutraceuticals or functional ingredients is increasingly widespread in human food; their use is also widespread in animal feed. These natural compounds generally come from plant materials and comprise a wide range of substances of a very diverse chemical nature. In animals, these compounds, so-called phytogenics, are used to obtain improvements in feed production/stability and also as functional components with repercussions on animal health. Along with polyphenols, isoprenoid compounds represent a family of substances with wide applications in therapy and pet nutrition. Essential oils (EOs) are a group of complex substances with fat-soluble nature that are widely used. Melatonin is an indolic amine present in all living with amphiphilic nature. In this work, we present a review of the most relevant phytogenics (polyphenol, isoprenoid, and alkaloid compounds), their characteristics, and possible uses as nutraceuticals in dogs, with special emphasis on EOs and their regulatory aspects, applied in foods and topically. Additionally, a presentation of the importance of the use of melatonin in dogs is developed, giving physiological and practical aspects about its use in dog feeding and also in topical application, with examples and future projections. This review points to the combination of EOs and melatonin in food supplements and in the topical application as an innovative product and shows excellent perspectives aimed at addressing dysfunctions in pets, such as the treatment of stress and anxiety, sleep disorders, alopecia, and hair growth problems, among others.

1. Introduction

Functional ingredients are increasingly used in diets to improve some aspects of health. Also called nutraceuticals, they are presented as complementary ingredients to diets that can help prevent possible diseases or dysfunctions. These functional ingredients are included in the diet as dietary supplements in the form of pills, capsules, liquids, or tablets, or they can also be included in foodstuffs as enrichers, reinforcing them [1,2]. Although we can find lists of functional ingredients according to their possible role in general health or specific dysfunctions, the most common is to classify them by their chemical structure or biosynthetic origin [3,4].
Table 1, Table 2 and Table 3 show detailed lists of the most widely used functional ingredients, mainly from plants, classified according to the chemical structure of active ingredients. We did not include those well-established functional ingredients in the food/feeds such as mono- and polyunsaturated fatty acids (MUFA, PUFA), vitamins (A, E, C, etc.), and the so-called prebiotics (polysaccharides, dietary fiber, short-chain fatty acids, etc.) and probiotics (live microorganisms) [4,5].
Polyphenols are a category of secondary plant metabolites that incorporates a large number and variety of compounds (Table 1) [6,7,8]. Such a variety of compounds incorporates a great variety of possible benefits, being able to find several beneficial effects for the same subclass and common effects in different classes and subclasses [9,10,11]. Of all the polyphenols studied as nutraceuticals or functional ingredients, we can highlight those that are better known as curcuminoids, betalains, and stilbenes, such as resveratrol, quinones as ubiquinol, and various flavonoids very studied, such as luteolin, genistein, hesperetin, quercetin, catechinsm and anthocyanidins (Table 1) [12,13].
Another group or class of functional ingredients of great interest are terpenes/terpenoids/isoprenoids (Table 2). These compounds of oily nature, but without being fatty acids, are widely distributed in the plant kingdom, constituting the first line of chemical defense for plants [14,15,16]. Monoterpenes and monoterpenoids are the main constituents of essential oils (EOs), which also contain, to a lesser extent, sesquiterpenoids and phenylpropanoids. Mono- and sesquiterpenoids have a huge variety of components, their most studied functions being antibacterial, antifungal, and antiviral, as well as antitumor and anti-inflammatory properties; their possible applications as neuro-protectors and as prebiotics have been recently studied. Triterpenes/triterpenoids are well known and used, especially phytosterols as cholesterol-lowering agents. Saponins and limonoids still have a wide field of study to cover, while steroid triterpenoids such as cardenolides, classified as cardiac glycosides, are widely applied in heart dysfunctions (Table 2) [12,17,18,19].
The list of known alkaloids is equally extensive, although in this case, their use as functional ingredients is much more restricted due to their more widespread action on the nervous system (Table 3). However, new functions of many alkaloids and new alkaloids with new properties are being discovered, which augur new functional applications [12,20,21]. We must highlight the notoriety of glucosinolates, nitrogenous compounds synthesized from amino acids with excellent health properties that, in recent years, have encouraged a large consumption of brassica vegetables such as broccoli, cauliflower, romanesco, cabbages, Brussel sprouts, Pak-choi, turnips, rutabaga, etc., which have the highest content of these interesting compounds that inhibit mitosis and can stimulate apoptosis in human tumor cells (Table 3) [22,23,24,25,26].

2. Essential Oils

Essential oils (EOs) are a complex mixture of oily volatile compounds generated by plants with eco-physiological functions related to the attraction or repulsion of insects and other herbivores. These oils are responsible for the distinctive aroma associated with individual plant species. EOs are generated in special plant structures (uni- or multicellular) such as glands, glandular hairs, papillae, generally named trichomes, and oil ducts. They are mainly found in leaves but also in fruits and flowers. The extraction of EOs, generally by the traditional technique of steam distillation and now by the modern supercritical carbon dioxide extraction technique, has very low yields (around 1%), generating highly concentrated volatile mixtures of EOs [16,27,28,29,30,31,32,33,34].
The composition of the EOs is diverse, depending on the plant species and chemo-types, which vary according to geographical and genetic parameters (chemical polymorphism) [35]. The bioactive compounds of EOs are terpenes and terpenoids, mainly mono-terpenoids (90%) and, in a small percentage, sesqui-, di- and triterpenoids; as very minority components appear some phenylpropanoids (see Table 1) and others (amino acids, polyketides, and sulfur compounds).
Generally, EOs are classified according to their molecular composition considering their main component. Thus, we find the different families of EOs and their denomination; we can cite an example: EOs mostly constituted by hydrocarbons with the ending -ene or -ane (α-pinene, limonene, menthane, carane); if they are alcohols, ending -ol (menthol, geraniol, farnesol), if they are aldehydes, ending -al (citral, neral), if they are ketones, ending -one (α-thujone, carvone, fenchone), if they are oxides, ending -ole (cineole, ascaridole) (Figure 1).
Table 4 shows some examples of EOs widely used as functional ingredients. This is a tiny sample of the number of EOs we can use. Although there are studies with some of the particular components of EOs (mainly terpenoids), most studies in therapy have been done with complete EOs, because it is very difficult to obtain pure samples of many of the components.
Regarding the possible beneficial actions of EOs, the successive scientific studies that are continually appearing generally come to give evidence of the extensive ethnopharmacological knowledge that has been accumulating throughout history and tradition, both from the Western, Asian, and African traditions. Table 1, Table 2 and Table 3 show, in general, many of the beneficial actions of functional ingredients. Among the properties of these ingredients of interest to the pet food sector, we can point out, from general actions for health valued as healthy, energetic, invigorating, restorative, anti-aging, etc., to more or less specific actions such as antibacterial, antifungal, antiviral, and antiparasitic. Additionally, ingredients with regulatory activities of metabolic functions related to cholesterol, triglycerides, glucose, ureides, etc. We can also mention the ingredients against pain, nausea, dizziness, hypertension, vasodilators, etc., and those with the protective systemic activity of the liver, kidneys, heart, lungs, and, also of urinary, circulatory, gastrointestinal, oral, and nasal systems. Of special interest are the compounds intended to regulate or improve mood and sleep, such as antidepressants, relaxants, anxiolytics and sedatives, and finally, those with an activating capacity of the immune system and with anticancer capabilities. Therefore, it is common to find in EOs specifications on health benefits such as analgesic, stimulant, narcotic, hyper-, hypotensive, bronchodilator, antimicrobial, anti-tumoral, vermicide, antimalarial, anticholinergic, cholagogue, emetic, cardiotonic, sympathetic, vasoconstrictor, etc. A whole presumed arsenal of natural compounds to improve and cope with the health dysfunctions of our pets. We must not forget that they are not drugs and, therefore, only proper and generally continued use could, presumably, alleviate some specific health dysfunctions [12].
According to the ECHA (European Chemicals Agency), EOs are defined as a volatile part of a natural product, which can be obtained by distillation, steam distillation, or pressing in the case of citrus fruits. It contains mostly volatile hydrocarbons. EOs are derived from various sections of plants and are “essential” in the sense that they carry a distinctive scent or essence of the plant. The European Federation of Essential Oils (EFEO) and the International Fragrance Association (IFRA) have published guidance for characterizing EOs. In feeds, EOs are studied, considered, and authorized by diverse European Food Safety Authority’s (EFSA) Panels such as Food Additives and Nutrient Sources added to Food, Additives and Products or Substances used in Animal Feed, which provides scientific advice on the safety and/or efficacy of additives and products or substances used in animal feed. These EFSA’s Panels, generally composed of renowned experts from Europe, evaluate their safety and/or efficacy for the target species, the user, the consumer of products of animal origin, and the environment. It also analyzes the efficacy of biological and chemical products/substances intended for deliberate use in animal feed. If EFSA’s opinion is favorable, the European Commission prepares a draft regulation to authorize the additive. This is then discussed and endorsed by the Member States represented in the Standing Committee on Plants, Animals, Food and Feed, Section Animal Nutrition [36]. Scientific opinions were reported in EFSA journals to be considered by the scientific community.
The components of EOs were studied and classified by EFSA, which provides an excellent database of food flavorings containing information on it [37], the FDA Office of Food Additive Safety (OFAS), and the Flavor and Extract Manufacturers Association of the United States (FEMA), founded in 1909, comprise flavor manufacturers, flavor users, flavor ingredient suppliers, and others with interest in the flavor industry, maintained available an online registered of flavorings, including EOs. Additionally, the International Organization of the Flavor Industry (IOFI), a global association representing the industry that creates, produces, and sells flavorings worldwide, provides excellent access to consult natural (complex) substance lists applied to food and feeds [38].
The EOs are more to be considered as flavorings. Generally, the EOs used in treating diseases in humans are also recommended for animals, with some exceptions, especially in cats. The use of EOs in animal/pet food requires, as in humans, some precautions and recommendations. According to the FDA, “GRAS” is an acronym for “Generally Recognized As Safe”. This term is applied to EOs. Most EOs and their components are classified as GRAS. FEMA, through its Food Additives Committee, has been publishing since 1960 multiple reports providing valuable information on EOs, giving their average dose of application and their maximum limits of use in various foods. Furthermore, since the publication of the first edition in 1971, Fenaroli’s Guide, a handbook that remains the standard reference for flavor ingredients worldwide, including GRAS substances recognized by FEMA and FDA [39]. In short, a Panel’s evaluation of an EOs or other substance performs a toxicity study observation, its relevance to observed effects on human/animal health is evaluated, and the dose at which no adverse effects (NOAEL) are observed is determined. NOAEL values are often used as reference points in the calculation of margins of safety (MOS) by taking the ratio between the NOAEL and the estimated intake for the substance under consideration. NOAEL values have commonly been used as a point of reference for the calculation of MOS, acceptable daily intake, and similar values by regulatory bodies. Mathematical modeling of the dose–response data was applied to estimate the benchmark dose corresponding to a specific change in response compared to the background, increasing relevance in safety evaluations [40].
According to the EC Regulation on additives for use in animal nutrition (EC1831/2003, Annex I), EOs could be included in different categories considering their possible action. Therefore, the added EOs can be considered a sensory additive if it exerts an improvement in the smell or palatability of the feed and also as a zootechnical additive, improving feed digestibility and/or gut microflora, but also as physiological stabilizers because the EOs can favorably affect animal health, for example by improving stress tolerance or safeguarding against possible infections. Although EOs can also be considered as technological additives, specifically as preservatives and antioxidants, protecting feed against deterioration by microorganism and oxidation [41,42]. In the United States, pet food products do not require premarket approval by the FDA.
Phytogenics is the term applied to plant-based compounds with some positive effects on animal growth and health. These phytogenics can occur in various forms, such as herbs, spices, raw plants and their extracts, oleoresins, EOs, vegetable oils, and hydrolates [43,44]. Very often, the format is not specified, being a very important feature to know its composition, characteristics, and possible beneficial possibilities in animal nutrition. In many cases, the lack of specificity in the type of phytogenic used has led to results largely inconsistent with limited understanding. Thus, to conduct systematic and comprehensive evaluations of the efficacy and safety of phytogenic compounds due to their complex composition, a better classification of phytogenics in animal nutrition studies may be necessary [43]. In addition to herbs and spices, widely used in feeds, EOs have been widely studied in animal nutrition, especially since restrictions on the use of antibiotics appeared. Studies on the bactericidal, fungicidal, and viricidal activities of many EOs are numerous, especially in pigs and poultry [45]. Also in dogs, there are numerous studies on EOs and their application as possible sepsis controllers [46,47,48,49,50].
Table 5 shows some examples of the use of EOs in dogs, indicating the dosage and possible beneficial effect. Generally, EOs have been used in dogs to improve their general health and immunological response, but also in specific therapies such as those aimed at improving liver, renal, cardiovascular, gastrointestinal, muscular-joint, and skin health, among others.
Although most of the applications of EOs are their topical use to avoid or reduce infestations and/or dermal affections [61], in some cases, EOs were included in food supplements, that is, as a nutritional supplement to the dog’s usual diet. Due to the lipophilic nature of the EOs, it is necessary to apply a fat matrix for perfect solubilization of the EOs, such as salmon oil. In this case, in addition to the beneficial qualities of salmon oil (richness in omega-3) and its natural content in tocopherols and carotenoids, the EOs come to complement their antioxidant properties. Increasing the intake of certain functional ingredients (vitamin D, omega-3 PUFA, phytogenic such as some essential oils and tea catechins) positively affects immunological function, improving defenses and reducing the risk of infection [67]. One of these products has recently been marketed, containing a range of EOs with functional specificities such as antiparasitic action, with savory, sagebrush, and clove EOs, or joint-articular improvement, with eucalyptus, ginger, and marjoram EOs [68].
Although EOs are classified as safe substances (GRAS) for use in animal nutrition, as discussed above, we cannot stress enough that aspects of animal food safety are crucial when using EOs. Gossypol toxicity is a well-known example. The intensive search for more affordable protein sources in fish nutrition in aquaculture led to the use of cottonseed protein concentrate, a product with excellent nutritional qualities, except for the existence of gossypol, a sesquiterpene aldehyde, toxic at accumulated high levels. The existence of gossypol causes intestinal inflammatory problems, as has been demonstrated in Nile tilapias, grass carps, and turbots, also in cattle acts as a cardiac and reproductive toxicant [69]. Perhaps, only ruminant microflora appears to have the ability to inactivate the presence of gossypol in feed [70].

3. Melatonin

Melatonin, an indoleamine synthesized from tryptophan and with multiple functions in mammals, was discovered in 1958 in cows [71] and in 1959 in humans [72,73]. This molecule, considered the sleep hormone, received this name due to its first studied action, its aggregator effect of melanocytes in frogs, tadpoles, and some fish, but not in mammals [71]. Melatonin is structurally N-acetyl-5-methoxytryptamine, a derivative of serotonin (5-hydroxytryptamine) that acts as a hormone on multiple endogenous rhythms such as temperature, mood, immune system, and other hormones and metabolic pathways [74,75,76,77]. Melatonin is secreted by the pineal gland to the cerebrospinal fluid and then to the bloodstream, with maximality during the middle of the night. The best-known action mechanism of melatonin is its regulatory role in sleep–wake cycles. Melatonin acts as a signal of darkness, providing information to the brain and other organs, synchronizing endocrine rhythms. Melatonin adjusts the timing of oscillator elements of the central and peripheral biological clocks. For this reason, melatonin is often recommended to relieve the symptoms of jet lag, a disorder in sleep rhythms due to transoceanic or long-haul flights crossing multiple time zones [78,79,80].
Melatonin is also an excellent antioxidant, presenting an antioxidant capacity several times greater than classical antioxidant molecules such as ascorbic acid, glutathione (GSH), and vitamin E. The scavenging activity of melatonin against reactive oxygen species (ROS) and reactive nitrogen species (RNS) has been clearly demonstrated by Reiter’s group and others, both in vitro and in vivo assays. This antioxidant action of melatonin has been reinforced by an antioxidative cascade that occurs due to the generation of some of its reaction products such as cyclic-3-hydroxymelatonin, N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK) and N1-acetyl-5-methoxykynuramine (AMK), in vitro and in vivo detected [81]. In addition, melatonin activates the expression of antioxidant enzymes in animal tissues in response to oxidative stress and exposure to toxic agents. Thus, superoxide dismutases (SOD), catalases, GSH peroxidases, GSH transferases, GSH synthases, and others are clearly up-regulated by melatonin to cope with possible distress situations. Generally, melatonin can regulate ROS/RNS levels by (i) a direct chemical action, scavenging its, in a receptor-independent action, and (ii) regulating antioxidant enzyme expression in a receptor-dependent action to control the redox network [82].
Although the possible beneficial actions of melatonin in diseases of mammals are very diverse (Figure 2) [83], relevant beneficial effects have been verified in studies on neurological dysfunctions (chronic fatigue, age-thermoregulation, migraine, multiple sclerosis, fibromyalgia, depression, schizophrenia, etc.), sleep disorders (jet-lag, insomnia, delayed sleep-phase, night-shift work sleep, sleep quality in blindness and autism), and others such as gastrointestinal, cardiovascular, in pre- and post-operative stress. Currently, research focuses on its role as an adjuvant in radio- and chemotherapies against several types of cancer, its role in neuro-dysfunctions such as Alzheimer’s and Parkinson’s, in diabetes and metabolic syndrome, and in immunological diseases, and its role as a relevant anti-inflammatory agent, having been proposed as a therapy against SARS-CoV-2 [74,75,84,85,86,87,88,89,90,91,92,93,94,95].
In dogs, melatonin has been used in various therapies. The use of melatonin is authorized, and it is the veterinarian who must prescribe its treatment in case of canine diseases or dysfunctions. Melatonin is usually given to the pet in the form of pills, powder, drops, or gelatin capsules, although it is often added to the feed in the form of a powder or liquid. It is also possible to apply it in creams or lotions in the case of skin treatments. There are at least three applications of interest related to melatonin. These are: (1) seasonal (recurrent) alopecia of the flanks; (2) anxiety and nervousness about noise or disorientation; and (3) sleep disorders in elderly dogs.

3.1. Seasonal (Recurrent) Alopecia of the Flanks

Cyclic flank alopecia is a follicular dysplasia characterized by altered coat quality, as well as alopecia that affects the sides and trunk [96]. As the skin is exposed, dry skin and hyperpigmentation frequently occur. It was thought to be due to seasonal changes, but it has been proven that, although seasonal changes can influence, it does not have to be related. It usually occurs cyclically or recurrently with loss of follicles and is of unknown etiology. Generally, the skin has no itching or inflammation. It usually occurs between autumn and winter. The breeds in which this process has been described the most are Boxer, Doberman, Rhodesian, Schnauzer, French and English Bulldog, and some types of Terriers such as Airedale. However, it can also appear in their crosses. A certain predisposition in females has also been described. Moreover, although initially it was believed that this alopecia was triggered by some hormonal imbalance, it has been shown that this is not the cause [96,97,98,99,100,101,102,103].
Melatonin intake seems to help in the regrowth of new hair, invigorating the hair follicles and giving rise to a renewed and healthy coat. In some recurrent breeds, melatonin is usually given as a preventive treatment a few weeks before the date on which alopecia occurred the previous year. In a Boxer dog study, the supply of 6 mg of melatonin per day induced partial hair regrowth in 2 months and its complete regeneration at 4 months [104]. Studies have also been described in which melatonin treatment has not been successful against alopecia, possibly due to a defect in dose or other causes [105,106]. In other dermatological assays in dogs, unequal results in melatonin treatments have been described [107].
A similar dysfunction, so-called Alopecia X (also known as an adrenal hyperplasia-like syndrome, hyperadrenocorticism, or Cushing’s syndrome), is characterized by partial to complete alopecia of the neck, tail, dorsum, perineum, thighs, and trunk. In addition, the skin may become hyperpigmented, primarily in areas of alopecia, occurring in both female and male young and adult dogs.
Behrend and Kennis (2010) review the possible hormonal aspects that affect Cushing’s syndrome (hyperadrenocorticism). With respect to melatonin, data and arguments for and against the syndrome were presented [108]. Thus, as data in favor, a trial with 29 dogs with Alopecia X in melatonin treatments at doses between 3 and 6 mg/kg, every 12 h for 4 months, where 15 of the patients showed hair regrowth [109]. Against in the same study, treating dogs with melatonin and mitotane (a toxic inhibitor of steroid hormone production that results in a decrease in cortisol levels), partial or complete hair regrowth was observed in only 62% of all dogs. Increasing the dose of melatonin in 8 dogs only showed hair regrowth in one of them. Of the five dogs whose hair did not grow back while receiving melatonin, two exhibited complete hair regrowth, one partial hair regrowth, and two were unable to regrow hair while receiving mitotane [109]. Additionally, in 15 Pomeranians with Alopecia X, melatonin (1.0–1.7 mg/kg, twice a day) for 3 months, only 40% had mild to moderate hair regrowth [110].
Mammalian skin is not only a target of melatonin bioactivity but also an important site of biosynthesis, regulation, and metabolism, where melatonin was detected in hair follicles as a modulator of hair growth and/or pigmentation [111,112], also as an antiaging cream treatment [113]. The scarce data on dogs are supported by previous studies on humans [114]. In a randomized controlled trial, women with androgenetic alopecia treated topically with daily 0.1% melatonin solutions for 6 months had a significant induction of the anagen phase of hair [115], not without criticism [116]. Additionally, in an open-label study of women and men with androgenetic alopecia, melatonin (33 ppm) topical application reduced the alopecia degree, and the TrichoScan technique showed a 29.2% increase in the hair count in 54.8% of patients after 3 months, and a 42.7% increase in 58.1% of patients after 6 months, demonstrating improvements in hair texture, decreased hair loss, and a reduction in seborrheic dermatitis, in safety and tolerant topical application of a cosmetic melatonin solution [117]. An exhaustive and recent revision of melatonin action in melanocyte physiology in humans and other mammals can be consulted [118].
In this regard, our preliminary data show that topical melatonin plus EOs application in dogs with Leishmaniosis showed a significant improvement in the affectation, decreasing the area of dermatitis, skin itching, and therefore, erosion wounds gradually improved in treatments with melatonin + EOs cream every 2 days, for 4–5 weeks (Figure 3).

3.2. Anxiety, Phobia, and Nervousness Due to Noise or Disorientation

Melatonin behaves as an anxiolytic molecule with relevant sedative and calming properties and is used to prevent or treat states of anxiety or depression [119,120,121,122,123,124,125,126], also in menopausal disorders [127]. In the surgical pre-operative, dogs treated with melatonin required lower doses of the anesthetic propofol due to the previous calming action of melatonin [128]. Additionally, similarly, the efficacy of pre-operative sedation with melatonin to reduce intraoperative use of midazolam (a benzodiazepine) in women under total abdominal hysterectomy [129]. As in humans, stress and distress are common problems in pets, and more so when they are alone at home. Taking advantage of the properties of melatonin as a mild sedative, veterinarians may recommend its use in situations of nervousness or phobia. Dogs tend to suffer from various forms of anxiety attacks. Some have noise phobias and get anxious due to thunderstorms, alarms, sirens, vacuum cleaners, and others. Other dogs show signs of anxiety when they must be put in a car. For others, anxiety appears with separation from the owner and being left alone. Many veterinarians treat nervous dogs with melatonin or sedative herbs before they experience the cause of anxiety, inhibiting it. It is advisable to administer a dose of melatonin at least half an hour before anxiety-provoking events occur. Recently, a direct relationship between the relaxing properties of medicinal plants such as valerian roots and phytomelatonin content has been described [130].

3.3. Sleep Disorders in Elderly Dogs

There are multiple pieces of evidence that melatonin deficiency in the blood tends to cause insomnia, especially in older dogs, as it also occurs in humans [131,132,133,134]. The use of melatonin as a nutraceutical in elderly dogs to treat insomnia and anxiety has been proposed [135,136]. Previously, Aronson (1999) suggested the use of melatonin with amitriptyline to manage thunderstorm phobia [137]. Additionally, Fourtillan et al., 2002 presented a study on beagle dogs with melatonin synthetic analogs suggesting that insomnia may be treated by administering hypnotic acetyl metabolites of melatonin or their synthetic analogs [138]. Some authors have recommended melatonin doses of 3–9 mg for dogs and 1.5–6 mg for cats to improve cognitive dysfunction syndrome, sleep-wake disturbances, and anxiety in older pets [139,140,141]. In a clinical study with 14 dogs on sleep behavior disorders, melatonin treatment showed uneven results. Thirteen of the dogs did not show any improvement in insomnia when treated with melatonin, but neither did they with gabapentin, diazepam, diphenhydramine, acepromazine, clonazepam, or phenobarbital. Only one dog had a positive response when 3 mg of melatonin (at night) was added to the potassium bromide treatment, and another dog was reported to have no response to an unknown dose of melatonin. Probably, according to the authors, dosing problems or frequency could explain these results [142]. Zanghi et al. (2016) suggested that in older dogs, the decrease in locomotor activity and insomnia could be related to a gradual degenerative neuronal disconnection between dorsal, dorso-medial, and ventral subparaventricular zones within the paraventral hypothalamic nucleus that regulates circadian melatonin release [143]. Additionally, in a comparative study, Lefman and Prittie (2019) proposed future studies to improve psychogenic stress in hospitalized veterinary patients treated with diazepam, midazolam, alprazolam, lorazepam, dexmedetomidine, trazodone, and melatonin, through therapies less aggressive and healthier [144]. Recently, Bódizs et al. (2020) presented a review on sleep in dogs, which includes the possible roles of melatonin [145].
In addition, the melatonin treatments can be of great help in elderly dogs or even in those that, due to vision problems, are unable to distinguish between daylight and darkness due to the beneficial action of melatonin on the retinal level [146,147].
Other applications of melatonin in dogs are under study. For example, extrapineal melatonin can act as a gastrointestinal protector [148,149,150], in oral surgery and implant dentistry, increasing bone-to-implant contact values and new bone formation [151,152,153], as regenerative in the skin [59,118], also as canine anti-tumoral agent [154,155,156,157].
Regarding possible side effects of melatonin in dogs, very few effects have been described if it is administered correctly and with the appropriate dose. In fact, it is the lack of secondary effects which often makes it a better choice than tranquilizers or other drugs [158]. However, there are some side effects that should be considered and your veterinarian should be informed about them, as they may recommend a lower dose or a different treatment. Some side effects that may occur are upset stomach and cramps, tachycardia, itching, and confusion.

4. Conclusions and Future Perspectives

In this review, an exhaustive list of phytogenics, their classification according to their chemical structure, and some of their beneficial properties were presented. Particular mention is made of essential oils, analyzing their composition and safety aspects, such as nutraceuticals for application in dogs. The most interesting cases and their uneven results were analyzed. As a synergistic therapy, results of the action of melatonin in dogs and also in humans were presented for its application in dysfunctions of interest. The combination of EOs and melatonin is presented as an innovative product of possible topical or oral administration, with excellent properties aimed at dysfunctions of great interest such as the treatment of stress and anxiety, sleep disorders, alopecia and hair growth problems, vision dysfunctions related to advanced age, improvements in the immune and gastrointestinal system, and antitumor actions, among others. Both components have excellent compatibility in terms of solubility, complemented by their respective antioxidant properties, ensuring the high stability of functional solutions [68,82,159,160,161,162].
However, the application of EOs and/or melatonin in pet foods presents some challenges to consider, such as (1) the correct dosage based on safety parameters, where the recommendations of the different authorized agencies (EFSA, FDA) are crucial; (2) ensuring the stability of components against industrial pet food techniques such as extrusion, sterilization, etc., is an important task considering wet or dry pet food formulae; (3) the functionality of the preparations involves important in vitro and in vivo scientific studies; (4) the innovative techniques of nanoencapsulation is presented as a tool to improve functionality and stability; (5) the preferential use of natural components over synthetic substances even with the handicap of cost, e.g., natural EOs versus analogous synthetic substances, and phytomelatonin (of plant origin) versus synthetic melatonin [163]; and (6) adequate information on the pet food labels in order to convey to consumers the most interesting aspects related to the functional properties of food supplements and their components.

Author Contributions

Concept, investigation, writing, D.R.-C.; resources, visualization, funding, G.S.-C.; methodology, data curation, investigation, A.E.-M.; concept, writing, review, project administration, supervision, M.B.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. DeFelice, S.L. The Nutraceutical Revolution: Its Impact on Food Industry R&D. Trends Food Sci. Technol. 1995, 6, 59–61. [Google Scholar]
  2. Pandey, M.; Verma, R.K.; Saraf, S.A. Nutraceuticals: New Era of Medicine and Health. Asian, J. Pharm. Clin. Res. 2010, 3, 11–15. [Google Scholar]
  3. Singh, J.; Sinha, S. Classification, Regulatory Acts And Applications Of Nutraceuticals for Health. Int. J. Pharma Biosci. 2012, 2, 177–187. [Google Scholar]
  4. da Costa, J.P. A Current Look at Nutraceuticals: Key Concepts and Future Prospects. Trends Food Sci. Technol. 2017, 62, 68–78. [Google Scholar] [CrossRef]
  5. Ruiz-Cano, D.; Sánchez-Carrasco, G.; Arnao, M.B. Current Vision of Functional Foods in the Diet of Cats and Dogs. All Pet Food Mag. 2020, 3, 12–13. [Google Scholar]
  6. Correia-da-Silva, M.; Sousa, E.; Pinto, M. Emerging Sulfated Flavonoids and Other Polyphenols as Drugs: Nature as an Inspiration. Med. Res. Rev. 2014, 34, 223–279. [Google Scholar] [CrossRef]
  7. Shahidi, F.; Ambigaipalan, P. Phenolics and Polyphenolics in Foods, Beverages and Spices: Antioxidant Activity and Health Effects. A Review. J. Funct. Foods 2015, 18, 820–897. [Google Scholar] [CrossRef]
  8. García-Conesa, M.T.; Larrosa, M. Polyphenol-Rich Foods for Human Health and Disease. Nutrients 2020, 12, 400. [Google Scholar] [CrossRef]
  9. Boy, F.R.; Casquete, R.; Martínez, A.; Córdoba, M.d.G.; Ruíz-Moyano, S.; Benito, M.J. Antioxidant, Antihypertensive and Antimicrobial Properties of Phenolic Compounds Obtained from Native Plants by Different Extraction Methods. Int. J. Environ. Res. Public Health 2021, 18, 2475. [Google Scholar] [CrossRef]
  10. Polia, F.; Pastor-Belda, M.; Martínez-Blázquez, A.; Horcajada, M.-N.; Tomás-Barberán, F.A.; García-Villalba, R. Technological and Biotechnological Processes To Enhance the Bioavailability of Dietary (Poly)Phenols in Humans. J. Agric. Food Chem. 2022, 70, 2092–2107. [Google Scholar] [CrossRef]
  11. Swallah, M.S.; Sun, H.; Affoh, R.; Fu, H.; Yu, H. Antioxidant Potential Overviews of Secondary Metabolites (Polyphenols) in Fruits. Int. J. Food Sci. 2020, 2020, e9081686. [Google Scholar] [CrossRef]
  12. Pengelly, A. The Constituents of Medicinal Plants, 3rd ed.; CABI: Wallingford, UK, 2021; ISBN 978-1-78924-307-9. [Google Scholar]
  13. Shen, N.; Wang, T.; Gan, Q.; Liu, S.; Wang, L.; Jin, B. Plant Flavonoids: Classification, Distribution, Biosynthesis, and Antioxidant Activity. Food Chem. 2022, 383, 132531. [Google Scholar] [CrossRef] [PubMed]
  14. Ashour, M.; Wink, M.; Gershenzon, J. Biochemistry of Terpenoids: Monoterpenes, Sesquiterpenes and Diterpenes. In Annual Plant Reviews: Biochemistry of Plant Secondary Metabolism; Wink, M., Ed.; Blackwell Pub.: New York, NY, USA, 2010; Volume 2, pp. 258–303. ISBN 978-1-4443-2050-3. [Google Scholar]
  15. de Alvarenga, J.F.R.; Genaro, B.; Costa, B.L.; Purgatto, E.; Manach, C.; Fiamoncini, J. Monoterpenes: Current Knowledge on Food Source, Metabolism, and Health Effects. Crit. Rev. Food Sci. Nutr. 2021, 1–38. [Google Scholar] [CrossRef] [PubMed]
  16. Masyita, A.; Mustika Sari, R.; Dwi Astuti, A.; Yasir, B.; Rahma Rumata, N.; Emran, T.B.; Nainu, F.; Simal-Gandara, J. Terpenes and Terpenoids as Main Bioactive Compounds of Essential Oils, Their Roles in Human Health and Potential Application as Natural Food Preservatives. Food Chem. X 2022, 13, 100217. [Google Scholar] [CrossRef] [PubMed]
  17. Crowell, P.L. Prevention and Therapy of Cancer by Dietary Monoterpenes. J. Nutr. 1999, 129, 775S–778S. [Google Scholar] [CrossRef]
  18. Santos, M.R.V.; Moreira, F.V.; Fraga, B.P.; de Souza, D.P.; Bonjardim, L.R.; Quintans-Junior, L.J. Cardiovascular Effects of Monoterpenes: A Review. Rev. Bras. Farmacogn. 2011, 21, 764–771. [Google Scholar] [CrossRef]
  19. Singh, B.; Sharma, R.A. Plant Terpenes: Defense Responses, Phylogenetic Analysis, Regulation and Clinical Applications. 3 Biotech 2015, 5, 129–151. [Google Scholar] [CrossRef]
  20. Dewick, P.M. Medicinal Natural Products; John Wiley & Sons, Ltd.: Chichester, UK, 2009; ISBN 978-0-470-74276-1. [Google Scholar]
  21. Mondal, A.; Gandhi, A.; Fimognari, C.; Atanasov, A.G.; Bishayee, A. Alkaloids for Cancer Prevention and Therapy: Current Progress and Future Perspectives. Eur. J. Pharmacol. 2019, 858, 172472. [Google Scholar] [CrossRef]
  22. Fahey, J.W.; Zalcmann, A.T.; Talalay, P. The Chemical Diversity and Distribution of Glucosinolates and Isothiocyanates among Plants. Phytochemistry 2001, 56, 5–51. [Google Scholar] [CrossRef]
  23. Halkier, B.A.; Gershenzon, J. Biology and Biochemistry of Glucosinolates. Annu. Rev. Plant Biol. 2006, 57, 303–333. [Google Scholar] [CrossRef]
  24. Verkerk, R.; Schreiner, M.; Krumbein, A.; Ciska, E.; Holst, B.; Rowland, I.; de Schrijver, R.; Hansen, M.; Gerhauser, C.; Mithen, R.; et al. Glucosinolates in Brassica Vegetables: The Influence of the Food Supply Chain on Intake, Bioavailability and Human Health. Mol. Nutr. Food Res. 2009, 53, S219–S265. [Google Scholar] [CrossRef]
  25. Selmar, D. Biosynthesis of Cyanogenic Glycosides, Glucosinolates and Non-Protein Amino Acids. In Annual Plant Reviews: Biochemistry of Plant Secondary Metabolism; Wink, M., Ed.; Blackwell Pub.: New York, NY, USA, 2010; Volume 2, pp. 92–181. ISBN 978-1-4443-2050-3. [Google Scholar]
  26. Hernández-Ruiz, J.; Ruiz-Cano, D.; Giraldo-Acosta, M.; Cano, A.; Arnao, M. Melatonin in Brassicaceae: Role in Postharvest and Interesting Phytochemicals. Molecules 2022, 27, 1523. [Google Scholar] [CrossRef] [PubMed]
  27. Scott, R.P.W. Essential Oils. In Encyclopedia of Analytical Science, 2nd ed.; Worsfold, P., Townshend, A., Poole, C., Eds.; Elsevier: Oxford, UK, 2005; pp. 554–561. ISBN 978-0-12-369397-6. [Google Scholar]
  28. Kaewwongse, M.; Sanesuwan, K.; Pupa, P.; Bullangpoti, V. Essential Oil Compounds as Stress Reducing Agents in Rats. Commun. Agric. Appl. Biol. Sci. 2013, 78, 167–172. [Google Scholar] [PubMed]
  29. Baser, K.H.C.; Buchbauer, G. (Eds.) Handbook of Essential Oils: Science, Technology, and Applications, 2nd ed.; CRC Press: Boca Raton, FL, USA, 2015; ISBN 978-0-429-15566-6. [Google Scholar]
  30. Kowalski, R.; Kowalska, G.; Jamroz, J.; Nawrocka, A.; Metyk, D. Effect of the Ultrasound-Assisted Preliminary Maceration on the Efficiency of the Essential Oil Distillation from Selected Herbal Raw Materials. Ultrason. Sonochem. 2015, 24, 214–220. [Google Scholar] [CrossRef]
  31. Rassem, H.H.A.; Nour, A.H.; Yunus, R.M. Techniques For Extraction of Essential Oils From Plants: A Review. Aust. J. Basic Appl. Sci. 2016, 10, 117–127. [Google Scholar]
  32. Ribeiro-Santos, R.; Andrade, M.; Sanches-Silva, A. Essential Oils. In Food Additives and Human Health; Bentham Science Publisher: Singapore, 2020; Volume 1, pp. 104–119. ISBN 9789811446139. [Google Scholar]
  33. Abd-ElGawad, A.M.; El Gendy, A.E.-N.G.; Assaeed, A.M.; Al-Rowaily, S.L.; Alharthi, A.S.; Mohamed, T.A.; Nassar, M.I.; Dewir, Y.H.; Elshamy, A.I. Phytotoxic Effects of Plant Essential Oils: A Systematic Review and Structure-Activity Relationship Based on Chemometric Analyses. Plants 2021, 10, 36. [Google Scholar] [CrossRef] [PubMed]
  34. Elshafie, H.S. Plant Essential Oil with Biological Activity. Plants 2022, 11, 980. [Google Scholar] [CrossRef]
  35. El Mihyaoui, A.; Esteves da Silva, J.C.G.; Charfi, S.; Candela Castillo, M.E.; Lamarti, A.; Arnao, M.B. Chamomile (Matricaria chamomilla L.): A Review of Ethnomedicinal Use, Phytochemistry and Pharmacological Uses. Life 2022, 12, 479. [Google Scholar] [CrossRef]
  36. EFSA. Available online: https://www.efsa.europa.eu/en/science/scientific-committee-and-panels/feedap#panel-members (accessed on 4 July 2022).
  37. EFSA2. Available online: https://webgate.ec.europa.eu/foods_system/main/?event=display (accessed on 4 July 2022).
  38. Novais, C.; Molina, A.K.; Abreu, R.M.V.; Santo-Buelga, C.; Ferreira, I.C.F.R.; Pereira, C.; Barros, L. Natural Food Colorants and Preservatives: A Review, a Demand, and a Challenge. J. Agric. Food Chem. 2022, 70, 2789–2805. [Google Scholar] [CrossRef]
  39. Burdock, G.A. Fenaroli’s Handbook of Flavor Ingredients, 6th ed.; CRC Press: Boca Raton, FL, USA, 2009; ISBN 978-0-429-15083-8. [Google Scholar]
  40. Kroes, R.; Galli, C.; Munro, I.; Schilter, B.; Tran, L.; Walker, R.; Würtzen, G. Threshold of Toxicological Concern for Chemical Substances Present in the Diet: A Practical Tool for Assessing the Need for Toxicity Testing. Food Chem. Toxicol. 2000, 38, 255–312. [Google Scholar] [CrossRef]
  41. Apak, R.; Capanoglu, E.; Shahidi, F. Measurement of Antioxidant Activity and Capacity: Recent Trends and Applications. In Hui: Food Science and Technology; Wiley: New York, NY, USA, 2018; ISBN 978-1-119-13535-7. [Google Scholar]
  42. Cano, A.; Arnao, M.B. ABTS/TEAC (2,2-Azino-Bis(3-Ethylbenzothiazoline-6-Sulfonic Acid)/Trolox-Equivalent Antioxidant Capacity) Radical Scavenging Mixed-Mode Assay. In Measurement of Antioxidant Activity & Capacity. Recent Trends and Applications; Apak, R., Capanoglu, E., Shahidi, F., Eds.; John Wiley & Sons: Oxford, UK, 2018; Volume 1, pp. 117–139. ISBN 978-1-119-13538-8. [Google Scholar]
  43. Yang, C.; Chowdhury, M.A.K.; Huo, Y.; Gong, J. Phytogenic Compounds as Alternatives to In-Feed Antibiotics: Potentials and Challenges in Application. Pathogens 2015, 4, 137–156. [Google Scholar] [CrossRef]
  44. Campigotto, G.; Jaguezeski, A.M.; Alba, D.F.; Giombelli, L.C.D.; da Rosa, G.; Souza, C.F.; Baldissera, M.D.; Petrolli, T.G.; da Silva, A.S. Microencapsulated Phytogenic in Dog Feed Modulates Immune Responses, Oxidative Status and Reduces Bacterial (Salmonella and Escherichia Coli) Counts in Feces. Microb. Pathog. 2021, 159, 105113. [Google Scholar] [CrossRef] [PubMed]
  45. Zhai, H.; Liu, H.; Wang, S.; Wu, J.; Kluenter, A.-M. Potential of Essential Oils for Poultry and Pigs. Anim. Nutr. 2018, 4, 179–186. [Google Scholar] [CrossRef] [PubMed]
  46. Ebani, V.V.; Nardoni, S.; Bertelloni, F.; Pistelli, L.; Mancianti, F. Antimicrobial Activity of Five Essential Oils against Bacteria and Fungi Responsible for Urinary Tract Infections. Molecules 2018, 23, 1668. [Google Scholar] [CrossRef] [PubMed]
  47. Meason-Smith, C.; Older, C.E.; Ocana, R.; Dominguez, B.; Lawhon, S.D.; Wu, J.; Patterson, A.P.; Rodrigues Hoffmann, A. Novel Association of Psychrobacter and Pseudomonas with Malodour in Bloodhound Dogs, and the Effects of a Topical Product Composed of Essential Oils and Plant-Derived Essential Fatty Acids in a Randomized, Blinded, Placebo-Controlled Study. Vet. Dermatol. 2018, 29, 465-e158. [Google Scholar] [CrossRef] [PubMed]
  48. Ludwig, A.; de Jesus, F.P.K.; Dutra, V.; Cândido, S.L.; Alves, S.H.; Santurio, J.M. Susceptibility Profile of Candida Rugosa (Diutina Rugosa) against Antifungals and Compounds of Essential Oils. J. Mycol. Med. 2019, 29, 154–157. [Google Scholar] [CrossRef] [PubMed]
  49. Bohmova, E.; Conkova, E.; Harcarova, M.; Sihelska, Z. Interactions between Clotrimazole and Selected Essential Oils against Malassezia Pachydermatis Clinical Isolates. Pol. J. Vet. Sci. 2019, 22, 173–175. [Google Scholar] [CrossRef] [PubMed]
  50. Sim, J.X.F.; Khazandi, M.; Chan, W.Y.; Trott, D.J.; Deo, P. Antimicrobial Activity of Thyme Oil, Oregano Oil, Thymol and Carvacrol against Sensitive and Resistant Microbial Isolates from Dogs with Otitis Externa. Vet. Dermatol. 2019, 30, 524-e159. [Google Scholar] [CrossRef]
  51. Komiya, M.; Sugiyama, A.; Tanabe, K.; Uchino, T.; Takeuchi, T. Evaluation of the Effect of Topical Application of Lavender Oil on Autonomic Nerve Activity in Dogs. Am. J. Vet. Res. 2009, 70, 764–769. [Google Scholar] [CrossRef]
  52. Godara, R.; Parveen, S.; Katoch, R.; Yadav, A.; Verma, P.K.; Katoch, M.; Kaur, D.; Ganai, A.; Raghuvanshi, P.; Singh, N.K. Acaricidal Activity of Extract of Artemisia Absinthium against Rhipicephalus Sanguineus of Dogs. Parasitol. Res. 2014, 113, 747–754. [Google Scholar] [CrossRef]
  53. Low, S.B.; Peak, R.M.; Smithson, C.W.; Perrone, J.; Gaddis, B.; Kontogiorgos, E. Evaluation of a Topical Gel Containing a Novel Combination of Essential Oils and Antioxidants for Reducing Oral Malodor in Dogs. Am. J. Vet. Res. 2014, 75, 653–657. [Google Scholar] [CrossRef]
  54. Monteiro, C.; Ferreira, L.L.; de Paula, L.G.F.; de Oliveira Filho, J.G.; de Oliveira Silva, F.; Muniz, E.R.; Menezes, K.M.F.; de Camargo, F.R.; de Oliveira Nonato, R.; Martins, D.B.; et al. Thymol and Eugenol Microemulsion for Rhiphicephalus Sanguineus Sensu Lato Control: Formulation Development, Field Efficacy, and Safety on Dogs. Vet. Parasitol. 2021, 296, 109501. [Google Scholar] [CrossRef]
  55. Goode, P.; Ellse, L.; Wall, R. Preventing Tick Attachment to Dogs Using Essential Oils. Ticks Tick Borne Dis. 2018, 9, 921–926. [Google Scholar] [CrossRef] [PubMed]
  56. Vercelli, C.; Pasquetti, M.; Giovannetti, G.; Visioni, S.; Re, G.; Giorgi, M.; Gambino, G.; Peano, A. In Vitro and in Vivo Evaluation of a New Phytotherapic Blend to Treat Acute Externa Otitis in Dogs. J. Vet. Pharmacol. Ther. 2021, 44, 910–918. [Google Scholar] [CrossRef] [PubMed]
  57. Gómez-García, M.; Madrigal, I.; Puente, H.; Mencía-Ares, Ó.; Argüello, H.; Carvajal, A.; Fregeneda-Grandes, J.M. In Vitro Activity of Essential Oils against Microbial Isolates from Otitis Externa Cases in Dogs. Nat. Prod. Res. 2021, 1–5. [Google Scholar] [CrossRef] [PubMed]
  58. Blaskovic, M.; Rosenkrantz, W.; Neuber, A.; Sauter-Louis, C.; Mueller, R.S. The Effect of a Spot-on Formulation Containing Polyunsaturated Fatty Acids and Essential Oils on Dogs with Atopic Dermatitis. Vet. J. 2014, 199, 39–43. [Google Scholar] [CrossRef]
  59. Catarino, M.; Combarros-Garcia, D.; Mimouni, P.; Pressanti, C.; Cadiergues, M.C. Control of Canine Idiopathic Nasal Hyperkeratosis with a Natural Skin Restorative Balm: A Randomized Double-Blind Placebo-Controlled Study. Vet. Dermatol. 2018, 29, 134-e53. [Google Scholar] [CrossRef]
  60. Schlieck, T.M.M.; Petrolli, T.G.; Bissacotti, B.F.; Copetti, P.M.; Bottari, N.B.; Morsch, V.M.; da Silva, A.S. Addition of a Blend of Essential Oils (Cloves, Rosemary and Oregano) and Vitamin E to Replace Conventional Chemical Antioxidants in Dog Feed: Effects on Food Quality and Health of Beagles. Arch. Anim. Nutr. 2021, 75, 389–403. [Google Scholar] [CrossRef]
  61. Michalczyk, A.; Ostrowska, P. Essential Oils and Their Components in Combating Fungal Pathogens of Animal and Human Skin. J. Mycol. Med. 2021, 31, 101118. [Google Scholar] [CrossRef]
  62. Nocera, F.P.; Mancini, S.; Najar, B.; Bertelloni, F.; Pistelli, L.; De Filippis, A.; Fiorito, F.; De Martino, L.; Fratini, F. Antimicrobial Activity of Some Essential Oils against Methicillin-Susceptible and Methicillin-Resistant Staphylococcus Pseudintermedius-Associated Pyoderma in Dogs. Animals 2020, 10, 1782. [Google Scholar] [CrossRef]
  63. Mondêgo-Oliveira, R.; de Sá Sousa, J.C.; Moragas-Tellis, C.J.; de Souza, P.V.R.; dos Santos Chagas, M.d.S.; Behrens, M.D.; de Jesús Hardoim, D.; Taniwaki, N.N.; Chometon, T.Q.; Bertho, A.L.; et al. Vernonia Brasiliana (L.) Druce Induces Ultrastructural Changes and Apoptosis-like Death of Leishmania Infantum Promastigotes. Biomed. Pharmacother. 2021, 133, 111025. [Google Scholar] [CrossRef]
  64. Rey-Valeirón, C.; Pérez, K.; Guzmán, L.; López-Vargas, J.; Valarezo, E. Acaricidal Effect of Schinus Molle (Anacardiaceae) Essential Oil on Unengorged Larvae and Engorged Adult Females of Rhipicephalus Sanguineus (Acari: Ixodidae). Exp. Appl. Acarol 2018, 76, 399–411. [Google Scholar] [CrossRef] [PubMed]
  65. da Silva, E.M.G.; Rodrigues, V.d.S.; Jorge, J.d.O.; Osava, C.F.; Szabó, M.P.J.; Garcia, M.V.; Andreotti, R. Efficacy of Tagetes Minuta (Asteraceae) Essential Oil against Rhipicephalus Sanguineus (Acari: Ixodidae) on Infested Dogs and in Vitro. Exp. Appl. Acarol. 2016, 70, 483–489. [Google Scholar] [CrossRef] [PubMed]
  66. Albuquerque, V.d.Q.; Soares, M.J.C.; Matos, M.N.C.; Cavalcante, R.M.B.; Guerrero, J.A.P.; Soares Rodrigues, T.H.; Gomes, G.A.; de Medeiros Guedes, R.F.; Castelo-Branco, D.d.S.C.M.; Goes da Silva, I.N.; et al. Anti-Staphylococcal Activity of Cinnamomum Zeylanicum Essential Oil against Planktonic and Biofilm Cells Isolated from Canine Otological Infections. Antibiotics 2022, 11, 4. [Google Scholar] [CrossRef] [PubMed]
  67. Bobeck, E.A. NUTRITION AND HEALTH: COMPANION ANIMAL APPLICATIONS: Functional Nutrition in Livestock and Companion Animals to Modulate the Immune Response. J. Anim. Sci. 2020, 98, skaa035. [Google Scholar] [CrossRef]
  68. Ruiz-Cano, D.; Sánchez-Carrasco, G.; Arnao, M.B. Food Supplements in Pet Food: An Example in Dogs with Essential Oils and Melatonin as Functional Ingredients. All Pet Food Magazine 2022, 4, 8–12. [Google Scholar]
  69. Li, W.-J.; Zhang, L.; Wu, H.-X.; Li, M.; Wang, T.; Zhang, W.-B.; Du, Z.-Y.; Zhang, M.-L. Intestinal Microbiota Mediates Gossypol-Induced Intestinal Inflammation, Oxidative Stress, and Apoptosis in Fish. J. Agric. Food Chem. 2022, 70, 6688–6697. [Google Scholar] [CrossRef]
  70. Zhang, Y.; Zhang, Z.; Dai, L.; Liu, Y.; Cheng, M.; Chen, L. Isolation and Characterization of a Novel Gossypol-Degrading Bacteria Bacillus Subtilis Strain Rumen Bacillus Subtilis. Asian-Australas J. Anim. Sci. 2018, 31, 63–70. [Google Scholar] [CrossRef]
  71. Lerner, A.B.; Case, J.D.; Takahashi, Y.; Lee, T.H.; Mori, W. Isolation of Melatonin, a Pineal Factor That Lightens Melanocytes. J. Am. Chem. Soc. 1958, 80, 2587. [Google Scholar] [CrossRef]
  72. Lerner, A.B.; Case, J.D.; Heinzelmann, R.V. Structure of Melatonin. J. Am. Chem. Soc. 1959, 81, 6084–6085. [Google Scholar] [CrossRef]
  73. Lerner, A.B.; Case, J.D.; Mori, W.; Wright, M.R. Melatonin in Peripheral Nerve. Nature 1959, 183, 1821. [Google Scholar] [CrossRef]
  74. Majidinia, M.; Reiter, R.J.; Shakouri, S.K.; Yousefi, B. The Role of Melatonin, a Multitasking Molecule, in Retarding the Processes of Ageing. Ageing Res. Rev. 2018, 47, 198–213. [Google Scholar] [CrossRef]
  75. Socaciu, A.I.; Ionut, R.; Socaciu, M.A.; Ungur, A.P.; Bârsan, M.; Chiorean, A.; Socaciu, C.; Râjnoveanu, A.G. Melatonin, an Ubiquitous Metabolic Regulator: Functions, Mechanisms and Effects on Circadian Disruption and Degenerative Diseases. Rev. Endocr. Metab. Disord. 2020, 21, 465–478. [Google Scholar] [CrossRef] [PubMed]
  76. Reiter, R.J.; Ma, Q.; Sharma, R. Melatonin in Mitochondria: Mitigating Clear and Present Dangers. Physiology 2020, 35, 86–95. [Google Scholar] [CrossRef] [PubMed]
  77. Fernández, V.G.; Reiter, R.J.; Agil, A. Melatonin Increases Brown Adipose Tissue Mass and Function in Zücker Diabetic Fatty Rats: Implications for Obesity Control. J. Pineal Res. 2018, 64, e12472. [Google Scholar] [CrossRef] [PubMed]
  78. Waterhouse, J.; Reilly, T.; Atkinson, G. Jet Lag. Lancet 1997, 350, 1611–1616. [Google Scholar] [CrossRef]
  79. Takahashi, T.; Sasaki, M.; Itoh, H.; Ozone, M.; Yamadera, W.; Hayshida, K.I.; Ushijima, S.; Matsunaga, N.; Obuchi, K.; Sano, H. Effect of 3 Mg Melatonin on Jet Lag Syndrome in an 8-h Eastward Flight. Psychiatry Clin. Neurosci. 2000, 54, 377–378. [Google Scholar] [CrossRef]
  80. Herxheimer, A. Jet Lag. Clin. Evid. 2005, 13, 2178–2183. [Google Scholar]
  81. Galano, A.; Tan, D.X.; Reiter, R.J. On the Free Radical Scavenging Activities of Melatonin’s Metabolites, AFMK and AMK. J. Pineal Res. 2013, 54, 245–257. [Google Scholar] [CrossRef]
  82. Arnao, M.; Hernández-Ruiz, J. Melatonin and Reactive Oxygen and Nitrogen Species: A Model for the Plant Redox Network. Melatonin Res. 2019, 2, 152–168. [Google Scholar] [CrossRef]
  83. Arnao, M.B.; Hernández-Ruiz, J. Melatonin: Synthesis from Tryptophan and Its Role in Higher Plants. In Amino Acids in Higher Plants; D’ Mello, J., Ed.; CAB Intern: Boston, MA, USA, 2015; pp. 390–435. ISBN 978-1-78064-263-5. [Google Scholar]
  84. Di Bella, G.; Mascia, F.; Gualano, L.; Di Bella, L. Melatonin Anticancer Effects: Review. Int. J. Mol. Sci. 2013, 14, 2410–2430. [Google Scholar] [CrossRef]
  85. Vadnie, C.A.; McClung, C.A. Circadian Rhythm Disturbances in Mood Disorders: Insights into the Role of the Suprachiasmatic Nucleus. Neural Plast. 2017, 2017, 1504507. [Google Scholar] [CrossRef]
  86. Xie, Z.; Chen, F.; Li, W.A.; Geng, X.; Li, C.; Meng, X.; Feng, Y.; Liu, W.; Yu, F. A Review of Sleep Disorders and Melatonin. Neurol. Res. 2017, 39, 559–565. [Google Scholar] [CrossRef]
  87. Alghamdi, B.S. The Neuroprotective Role of Melatonin in Neurological Disorders. J. Neurosci. Res. 2018, 96, 1136–1149. [Google Scholar] [CrossRef] [PubMed]
  88. Blume, C.; Angerer, M.; Raml, M.; del Giudice, R.; Santhi, N.; Pichler, G.; Kunz, A.B.; Scarpatetti, M.; Trinka, E.; Schabus, M. Healthier Rhythm, Healthier Brain? Integrity of Circadian Melatonin and Temperature Rhythms Relates to the Clinical State of Brain-Injured Patients. Eur. J. Neurol. 2019, 26, 1051–1059. [Google Scholar] [CrossRef] [PubMed]
  89. Pandi-Perumal, S.R.; Cardinali, D.; Reiter, R.; Brown, G. Low Melatonin as a Contributor to SARS-CoV-2 Disease. Melatonin Res. 2020, 3, 558–576. [Google Scholar] [CrossRef]
  90. Cardinali, D.; Brown, G.; Pandi-Perumal, S.R. Can Melatonin Be a Potential “Silver Bullet” in Treating COVID-19 Patients? Diseases 2020, 8, 44. [Google Scholar] [CrossRef]
  91. Cardinali, D.P. Melatonin and Healthy Aging. In Vitamins and Hormones Hormones and Aging; Litwack, G., Ed.; Academic Press: Cambridge, MA, USA, 2021; Volume 115, pp. 67–88. ISBN 0083-6729. [Google Scholar]
  92. Santos-Ledo, A.; de Luxán-Delgado, B.; Caballero, B.; Potes, Y.; Rodríguez-González, S.; Boga, J.A.; Coto-Montes, A.; García-Macia, M. Melatonin Ameliorates Autophagy Impairment in a Metabolic Syndrome Model. Antioxidants 2021, 10, 796. [Google Scholar] [CrossRef]
  93. Delpino, F.M.; Figueiredo, L.M.; Nunes, B.P. Effects of Melatonin Supplementation on Diabetes: A Systematic Review and Meta-Analysis of Randomized Clinical Trials. Clin. Nutr. 2021, 40, 4595–4605. [Google Scholar] [CrossRef]
  94. Lauritzen, E.S.; Kampmann, U.; Pedersen, M.G.B.; Christensen, L.-L.; Jessen, N.; Møller, N.; Støy, J. Three Months of Melatonin Treatment Reduces Insulin Sensitivity in Patients with Type 2 Diabetes—A Randomized Placebo-Controlled Crossover Trial. J. Pineal Res. 2022, 73, e12809. [Google Scholar] [CrossRef]
  95. Okeke, E.S.; Ogugofor, M.O.; Nkwoemeka, N.E.; Nweze, E.J.; Okoye, C.O. Phytomelatonin: A Potential Phytotherapeutic Intervention on COVID-19-Exposed Individuals. Microbes Infect. 2022, 24, 104886. [Google Scholar] [CrossRef]
  96. Murayama, N.; Takahashi, S.; Hizume, T.; Nagata, M. Canine Recurrent Flank Alopecia with Hair Loss on the Nose Bridge and the Pinnae in a Family of Airedale Terrier. Jpn J. Vet. Dermatol. 2005, 11, 1–4. [Google Scholar] [CrossRef]
  97. Scott, D. Seasonal Flank Alopecia in Ovariohysterectomized Dogs. Cornell Vet. 1990, 80, 187–195. [Google Scholar] [PubMed]
  98. Waldman, L. Seasonal Flank Alopecia in Affenpinschers. J. Small Anim. Pract. 1995, 36, 271–273. [Google Scholar] [CrossRef] [PubMed]
  99. Curtis, C.F.; Evans, H.; Lloyd, D.H. Investigation of the Reproductive and Growth Hormone Status of Dogs Affected by Idiopathic Recurrent Flank Alopecia. J. Small Anim. Pract. 1996, 37, 417–422. [Google Scholar] [CrossRef]
  100. Ando, J.; Nagata, M. Seasonal Flank Alopecia in a Boxer. Jpn. J. Vet. Dermatol. 2000, 6, 17–20. [Google Scholar] [CrossRef]
  101. Paradis, M. Melatonin Therapy in Canine Alopecia. In Kirk’s Current Veterinary Therapy XIII Small Animal Practice; WB Saunders Company: Philadelphia, PA, USA, 2000; pp. 546–549. [Google Scholar]
  102. van der Luer, R.; Bonestroo, J. A dog with an unusual case of alopecia; case report. Tijdschr. Diergeneeskd. 2010, 135, 492–494. [Google Scholar] [PubMed]
  103. Miller, W.H., Jr.; Griffin, C.E.; Campbell, K.L. Muller and Kirk’s Small Animal Dermatology; Elsevier Health Sciences: St Louis, MO, USA, 2012; ISBN 1-4160-0028-3. [Google Scholar]
  104. Rachid, M.A.; Demaula, C.D.; Scott, D.W.; Miller, W.H.; Senter, D.A.; Myers, S. Concurrent Follicular Dysplasia and Interface Dermatitis in Boxer Dogs. Vet. Dermatol. 2003, 14, 159–166. [Google Scholar] [CrossRef]
  105. Diaz, S.F.; Torres, S.M.F.; Nogueira, S.a.F.; Gilbert, S.; Jessen, C.R. The Impact of Body Site, Topical Melatonin and Brushing on Hair Regrowth after Clipping Normal Siberian Husky Dogs. Vet. Dermatol. 2006, 17, 45–50. [Google Scholar] [CrossRef]
  106. Perego, R.; Proverbio, D.; Roccabianca, P.; Spada, E. Color Dilution Alopecia in a Blue Doberman Pinscher Crossbreed. Can. Vet. J. 2009, 50, 511–514. [Google Scholar]
  107. Rees, C.A. New Drugs in Veterinary Dermatology. Vet. Clin. N. Am. Small Anim. Pract. 1999, 29, 1449–1460. [Google Scholar] [CrossRef]
  108. Behrend, E.N.; Kennis, R. Atypical Cushing’s Syndrome in Dogs: Arguments For and Against. Vet. Clin. N. Am. Small Anim. Pract. 2010, 40, 285–296. [Google Scholar] [CrossRef]
  109. Frank, L.A.; Hnilica, K.A.; Oliver, J.W. Adrenal Steroid Hormone Concentrations in Dogs with Hair Cycle Arrest (Alopecia X) before and during Treatment with Melatonin and Mitotane. Vet. Dermatol. 2004, 15, 278–284. [Google Scholar] [CrossRef] [PubMed]
  110. Frank, L.A.; Donnell, R.L.; Kania, S.A. Oestrogen Receptor Evaluation in Pomeranian Dogs with Hair Cycle Arrest (Alopecia X) on Melatonin Supplementation. Vet. Dermatol. 2006, 17, 252–258. [Google Scholar] [CrossRef] [PubMed]
  111. Slominski, A.; Fischer, T.W.; Zmijewski, M.A.; Wortsman, J.; Semak, I.; Zbytek, B.; Slominski, R.M.; Tobin, D.J. On the Role of Melatonin in Skin Physiology and Pathology. Endocrine 2005, 27, 137–147. [Google Scholar] [CrossRef]
  112. Slominski, A.; Tobin, D.J.; Zmijewski, M.A.; Wortsman, J.; Paus, R. Melatonin in the Skin: Synthesis, Metabolism and Functions. Trends Endocrinol. Metabol. 2008, 19, 17–24. [Google Scholar] [CrossRef] [PubMed]
  113. Milani, M.; Sparavigna, A. Antiaging Efficacy of Melatonin-Based Day and Night Creams: A Randomized, Split-Face, Assessor-Blinded Proof-of-Concept Trial. Clin. Cosmet. Investig. Dermatol. 2018, 11, 51–57. [Google Scholar] [CrossRef]
  114. Fischer, T.W.; Slominski, A.; Tobin, D.J.; Paus, R. Melatonin and the Hair Follicle. J. Pineal Res. 2008, 44, 1–15. [Google Scholar] [CrossRef]
  115. Fischer, T.W.; Burmeister, G.; Schmidt, H.W.; Elsner, P. Melatonin Increases Anagen Hair Rate in Women with Androgenetic Alopecia or Diffuse Alopecia: Results of a Pilot Randomized Controlled Trial. Br. J. Dermatol. 2004, 150, 341–345. [Google Scholar] [CrossRef]
  116. Sladden, M.J.; Hutchinson, P.E. Is Melatonin Useful in Alopecia: Critical Appraisal of a Randomized Trial? Br. J. Dermatol. 2005, 153, 859–860. [Google Scholar] [CrossRef]
  117. Fischer, T.W.; Trüeb, R.M.; Hänggi, G.; Innocenti, M.; Elsner, P. Topical Melatonin for Treatment of Androgenetic Alopecia. Int. J. Trichology 2012, 4, 236. [Google Scholar] [CrossRef]
  118. Sevilla, A.; Chéret, J.; Slominski, R.M.; Slominski, A.T.; Paus, R. Revisiting the Role of Melatonin in Human Melanocyte Physiology: A Skin Context Perspective. J. Pineal Res. 2022, 72, e12790. [Google Scholar] [CrossRef]
  119. Dahlitz, M.; Alvarez, B.; Vignau, J.; English, J.; Arendt, J.; Parkes, J. Delayed Sleep Phase Syndrome Response to Melatonin. Lancet 1991, 337, 1121–1124. [Google Scholar] [CrossRef]
  120. Jan, J.; Hamilton, D.; Seward, N.; Fast, D.; Freeman, R.; Laudon, M. Clinical Trial of Controlled-Release Melatonin in Children with Sleep-Wake Disorders. J. Pineal Res. 2000, 29, 34–39. [Google Scholar] [CrossRef] [PubMed]
  121. Naranjo-Rodríguez, E.B.; Osornio, A.O.; Hernández-Avitia, E.; Mendoza-Fernández, V.; Escobar, A. Anxiolytic-like Actions of Melatonin, 5-Metoxytryptophol, 5-Hydroxytryptophol and Benzodiazepines on a Conflict Procedure. Prog. Neuro-Psychopharmacol. Biol. Psychiatry 2000, 24, 117–129. [Google Scholar] [CrossRef]
  122. Ferracioli-Oda, E.; Qawasmi, A.; Bloch, M.H. Meta-Analysis: Melatonin for the Treatment of Primary Sleep Disorders. PLoS ONE 2013, 8, e63773. [Google Scholar] [CrossRef]
  123. Chen, Z.; Xie, Y.; Gu, Q.; Zhao, G.; Zhang, Y.; Cui, W.; Xu, S.; Wang, R.; Shen, W. The AtrbohF-Dependent Regulation of ROS Signaling Is Required for Melatonin-Induced Salinity Tolerance in Arabidopsis. Free. Radic. Biol. Med. 2017, 108, 465–477. [Google Scholar] [CrossRef] [PubMed]
  124. Huang, F.; Yang, Z.; Li, C.-Q. The Melatonergic System in Anxiety Disorders and the Role of Melatonin in Conditional Fear. Vitam. Horm. 2017, 103, 281–294. [Google Scholar]
  125. Li, C.; Ma, D.; Li, M.; Wei, T.; Zhao, X.; Heng, Y.; Ma, D.; Anto, E.O.; Zhang, Y.; Niu, M.; et al. The Therapeutic Effect of Exogenous Melatonin on Depressive Symptoms: A Systematic Review and Meta-Analysis. Front. Psychiatry 2022, 13, 737972. [Google Scholar] [CrossRef]
  126. Kholghi, G.; Eskandari, M.; Shokouhi Qare Saadlou, M.-S.; Zarrindast, M.-R.; Vaseghi, S. Night Shift Hormone: How Does Melatonin Affect Depression? Physiol. Behav. 2022, 252, 113835. [Google Scholar] [CrossRef]
  127. Tandon, V.R.; Sharma, S.; Mahajan, A.; Mahajan, A.; Tandon, A. Menopause and Sleep Disorders. J. Midlife Health 2022, 13, 26–33. [Google Scholar] [CrossRef]
  128. Niggemann, J.R.; Tichy, A.; Eberspächer-Schweda, M.C.; Eberspächer-Schweda, E. Preoperative Calming Effect of Melatonin and Its Influence on Propofol Dose for Anesthesia Induction in Healthy Dogs. Vet. Anaesth. Analg. 2019, 46, 560–567. [Google Scholar] [CrossRef]
  129. Rosas-Luna, L.E.; Castelán-Martínez, O.D.; Mora-Magaña, I.; Ángeles-Castellanos, M.; Ubaldo-Reyes, L.M. Midazolam Reduction with Pre-Operative Melatonin in Abdominal Hysterectomy: Double-Blind Randomized Clinical Trial. Cir. Cir. 2022, 90, 353–358. [Google Scholar] [CrossRef] [PubMed]
  130. Losada, M.; Cano, A.; Hernández-Ruiz, J.; Arnao, M.B. Phytomelatonin Content in Valeriana Officinalis L. and Some Related Phytotherapeutic Supplements. Int. J. Plant Based Pharm. 2022, 2, 176–181. [Google Scholar] [CrossRef]
  131. Lyseng-Williamson, K.A. Melatonin Prolonged Release: In the Treatment of Insomnia in Patients Aged >= 55 Years. Drugs Aging 2012, 29, 911–923. [Google Scholar] [CrossRef]
  132. Pfeffer, M.; Korf, H.-W.; Wicht, H. Synchronizing Effects of Melatonin on Diurnal and Circadian Rhythms. Gen. Comp. Endocrinol. 2018, 258, 215–221. [Google Scholar] [CrossRef]
  133. Hull, J.T.; Czeisler, C.A.; Lockley, S.W. Suppression of Melatonin Secretion in Totally Visually Blind People by Ocular Exposure to White Light: Clinical Characteristics. Ophthalmology 2018, 125, 1160–1171. [Google Scholar] [CrossRef] [PubMed]
  134. Bologna, C.; Madonna, P.; Pone, E. Efficacy of Prolonged-Release Melatonin 2 Mg (PRM 2 Mg) Prescribed for Insomnia in Hospitalized Patients for COVID-19: A Retrospective Observational Study. J. Clin. Med. 2021, 10, 5857. [Google Scholar] [CrossRef]
  135. Simpson, B.S.; Papich, M.G. Pharmacologic Management in Veterinary Behavioral Medicine. Vet. Clin. N. Am. Small Anim. Pract. 2003, 33, 365–404. [Google Scholar] [CrossRef]
  136. Mandelker, L.; Wynn, S. Cellular Effects of Common Nutraceuticals and Natural Food Substances. Vet. Clin. N. Am. Small Anim. Pract. 2004, 34, 339–353. [Google Scholar] [CrossRef]
  137. Aronson, L. Animal Behavior Case of the Month. A Dog Was Evaluated Because of Extreme Fear. J. Am. Vet. Med. Assoc. 1999, 215, 22–24. [Google Scholar]
  138. Fourtillan, J.B. Role of Melatonin in the Induction and Maintenance of Sleep. Dialogues Clin. Neurosci. 2002, 4, 395–401. [Google Scholar] [CrossRef]
  139. Landsberg, G.M.; Nichol, J.; Araujo, J.A. Cognitive Dysfunction Syndrome: A Disease of Canine and Feline Brain Aging. Vet. Clin. N. Am. Small Anim. Pract. 2012, 42, 749–768. [Google Scholar] [CrossRef] [PubMed]
  140. Landsberg, G.M.; DePorter, T.; Araujo, J.A. Clinical Signs and Management of Anxiety, Sleeplessness, and Cognitive Dysfunction in the Senior Pet. Vet. Clin. N. Am. Small Anim. Pract. 2011, 41, 565–590. [Google Scholar] [CrossRef] [PubMed]
  141. Landsberg, G. Therapeutic Options for Cognitive Decline in Senior Pets. J. Am. Anim. Hosp. Assoc. 2006, 42, 407–413. [Google Scholar] [CrossRef] [PubMed]
  142. Schubert, T.A.; Chidester, R.M.; Chrisman, C.L. Clinical Characteristics, Management and Long-Term Outcome of Suspected Rapid Eye Movement Sleep Behaviour Disorder in 14 Dogs. J. Small Anim. Pract. 2011, 52, 93–100. [Google Scholar] [CrossRef] [PubMed]
  143. Zanghi, B.M.; Gardner, C.; Araujo, J.; Milgram, N.W. Diurnal Changes in Core Body Temperature, Day/Night Locomotor Activity Patterns, and Actigraphy-Generated Behavioral Sleep in Aged Canines with Varying Levels of Cognitive Dysfunction. Neurobiol. Sleep Circadian Rhythm. 2016, 1, 8–18. [Google Scholar] [CrossRef] [PubMed]
  144. Lefman, S.H.; Prittie, J.E. Psychogenic Stress in Hospitalized Veterinary Patients: Causation, Implications, and Therapies. J. Vet. Emerg. Crit. Care 2019, 29, 107–120. [Google Scholar] [CrossRef]
  145. Bódizs, R.; Kis, A.; Gácsi, M.; Topál, J. Sleep in the Dog: Comparative, Behavioral and Translational Relevance. Curr. Opin. Behav. Sci. 2020, 33, 25. [Google Scholar] [CrossRef]
  146. Zmijewski, M.A.; Sweatman, T.W.; Slominski, A.T. The Melatonin-Producing System Is Fully Functional in Retinal Pigment Epithelium. Mol. Cell Endocrinol. 2009, 307, 211–216. [Google Scholar] [CrossRef]
  147. Agorastos, A.; Huber, C.G. The Role of Melatonin in Glaucoma: Implications Concerning Pathophysiological Relevance and Therapeutic Potential. J. Pineal Res. 2011, 50, 1–7. [Google Scholar] [CrossRef]
  148. Bubenik, G. Gastrointestinal Melatonin: Localization, Function, and Clinical Revelance. Diges Dis. Sci. 2002, 47, 2336–2348. [Google Scholar] [CrossRef]
  149. Sommansson, A.; Yamskova, O.; Schiöth, H.B.; Nylander, O.; Sjöblom, M. Long-Term Oral Melatonin Administration Reduces Ethanol-Induced Increases in Duodenal Mucosal Permeability and Motility in Rats. Acta Physiol. 2014, 212, 152–165. [Google Scholar] [CrossRef] [PubMed]
  150. Vollmer, C.; Weber, A.P.M.; Wallenfang, M.; Hoffmann, T.; Mettler-Altmann, T.; Truse, R.; Bauer, I.; Picker, O.; Mathes, A.M. Melatonin Pretreatment Improves Gastric Mucosal Blood Flow and Maintains Intestinal Barrier Function during Hemorrhagic Shock in Dogs. Microcirculation 2017, 24, e12345. [Google Scholar] [CrossRef] [PubMed]
  151. Muñoz, F.; López-Peña, M.; Miño, N.; Gómez-Moreno, G.; Guardia, J.; Cutando, A. Topical Application of Melatonin and Growth Hormone Accelerates Bone Healing around Dental Implants in Dogs. Clin. Implant Dent. Relat. Res. 2012, 14, 226–235. [Google Scholar] [CrossRef] [PubMed]
  152. Gómez-Moreno, G.; Aguilar-Salvatierra, A.; Boquete-Castro, A.; Guardia, J.; Piattelli, A.; Perrotti, V.; Delgado-Ruiz, R.A.; Calvo-Guirado, J.L. Outcomes of Topical Applications of Melatonin in Implant Dentistry: A Systematic Review. Implant Dent. 2015, 24, 25–30. [Google Scholar] [CrossRef] [PubMed]
  153. Arora, H.; Ivanovski, S. Melatonin as a Pro-Osteogenic Agent in Oral Implantology: A Systematic Review of Histomorphometric Outcomes in Animals and Quality Evaluation Using ARRIVE Guidelines. J. Periodontal Res. 2017, 52, 151–161. [Google Scholar] [CrossRef]
  154. Lopes, J.R.; Maschio, L.B.; Jardim-Perassi, B.V.; Moschetta, M.G.; Ferreira, L.C.; Martins, G.R.; Gelaleti, G.B.; De Campos Zuccari, D.A.P. Evaluation of Melatonin Treatment in Primary Culture of Canine Mammary Tumors. Oncol. Rep. 2015, 33, 311–319. [Google Scholar] [CrossRef]
  155. Gonçalves, N.d.N.; Colombo, J.; Lopes, J.R.; Gelaleti, G.B.; Moschetta, M.G.; Sonehara, N.M.; Hellmén, E.; de Zanon, C.F.; Oliani, S.M.; Zuccari, D.A.P. de C. Effect of Melatonin in Epithelial Mesenchymal Transition Markers and Invasive Properties of Breast Cancer Stem Cells of Canine and Human Cell Lines. PLoS ONE 2016, 11, e0150407. [Google Scholar] [CrossRef]
  156. Custódio, P.R.; Colombo, J.; Ventura, F.V.; Castro, T.B.; Zuccari, D.A.P.C. Melatonin Treatment Combined with TGF-β Silencing Inhibits Epithelial- Mesenchymal Transition in CF41 Canine Mammary Cancer Cell Line. Anticancer Agents Med. Chem. 2020, 20, 989–997. [Google Scholar] [CrossRef]
  157. Kohandel, Z.; Farkhondeh, T.; Aschner, M.; Samarghandian, S. Molecular Targets for the Management of Gastrointestinal Cancer Using Melatonin, a Natural Endogenous Body Hormone. Biomed. Pharmacother. 2021, 140, 111782. [Google Scholar] [CrossRef]
  158. Andersen, L.P.H.; Gögenur, I.; Rosenberg, J.; Reiter, R.J. The Safety of Melatonin in Humans. Clin. Drug. 2016, 36, 169–175. [Google Scholar] [CrossRef]
  159. Cano, A.; Alcaraz, O.; Arnao, M.B. Free Radical-Scavenging Activity of Indolic Compounds in Aqueous and Ethanolic Media. Anal. Bioanal. Chem. 2003, 376, 33–37. [Google Scholar] [CrossRef] [PubMed]
  160. Arnao, M.B.; Hernández-Ruiz, J. The Potential of Phytomelatonin as a Nutraceutical. Molecules 2018, 23, 238. [Google Scholar] [CrossRef] [PubMed]
  161. Arnao, M.B.; Hernández-Ruiz, J. Phytomelatonin, Natural Melatonin from Plants as a Novel Dietary Supplement: Sources, Activities and World Market. J. Funct. Foods 2018, 48, 37–42. [Google Scholar] [CrossRef]
  162. Bonomini, F.; Borsani, E.; Favero, G.; Rodella, L.F.; Rezzani, R. Dietary Melatonin Supplementation Could Be a Promising Preventing/Therapeutic Approach for a Variety of Liver Diseases. Nutrients 2018, 10, 1135. [Google Scholar] [CrossRef]
  163. Pérez-Llamas, F.; Hernández-Ruiz, J.; Cuesta, A.; Zamora, S.; Arnao, M.B. Development of a Phytomelatonin-Rich Extract from Cultured Plants with Excellent Biochemical and Functional Properties as an Alternative to Synthetic Melatonin. Antioxidants 2020, 9, 158. [Google Scholar] [CrossRef]
Figure 1. Molecular structures of some EO components.
Figure 1. Molecular structures of some EO components.
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Figure 2. Roles of melatonin in mammals at cellular/physiological level. Their use in several disorders is shown in green color.
Figure 2. Roles of melatonin in mammals at cellular/physiological level. Their use in several disorders is shown in green color.
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Figure 3. Photographs of different areas of the animal showing different affectations before the treatment (photos on the left) and 24 days after the treatment with 11 topical applications (photos on the right).
Figure 3. Photographs of different areas of the animal showing different affectations before the treatment (photos on the left) and 24 days after the treatment with 11 topical applications (photos on the right).
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Table 1. Natural functional ingredients and potential benefits: polyphenols.
Table 1. Natural functional ingredients and potential benefits: polyphenols.
Chemical Category/ClassChemical Name/SubclassExample of CompoundsPotential Benefits
Phenylpropanoids
Simple phenolsArbutin, tyrosolAntiseptic, diuretic, anti-tumoral
Hydroxycinnamic acids
Free forms
Esters
Alcohols, Aldehydes
& Glycosides
Ferulic, caffeic, cinnamic
Chlorogenic, rosmarinic, cynarin, cichoric, caftaric
Coniferyl, caffeoyl, feruloyl, vanillin, eugenol
Antioxidant, chemoprotector, immunomodulatory, neuroprotector, dyspepsia, hypercholesterolemia
AcetophenonesApocynin, androsin,
piceol, picein
Antiasthmatic, anti-inflammatory, neuroprotective, sedative
SalicylatesSalicin, salicortin, populinAnalgesic, febrifuges, sciatica, myalgia
CurcuminoidsCurcumin, dimethoxy- and bisdemethoxy-curcumin, and breakdown metabolitesAnti-inflammatory, anti-tumoral, cardioprotective, wound healing, anti-arthritis, antioxidant, anti-depressive
Lignans & NeolignansPinoresinol, masoprocol, silybin, schizandrin, podophyllotoxin, enterodiolHypoglycemic, chemoprotector, antioxidant, keratosis, antifungal, anti-inflammatory, anti-tumoral, phytoestrogen precursors
Coumarins & FuranocoumarinsCoumarin, aesculetin, xanthotoxin, umbelliferone, psoralen, angelican, bergapten, khellinPhotosensitizer, anti-vitiligo, psoriasis, tinea hypopigmentation, spasmolytic, bronchodilator, asthma, anti-hypertensive, renal calculi, hay fever, rhinitis
Betalains
Betacyanins
Betaxanthins
Betanin, (iso-, pro-, neo-)
Vulga-xanthin
(mira-, portula-, indica-)
Antioxidant, antimicrobial, anti-tumoral
Polyketide-derived
StilbenesResveratrol, pinosylvin, piceatannol, piceid, pallidol, viniferin, pterostylbeneAnti-inflammatory, neuroprotective, anti-tumoral, cardioprotective, anti-aging, antioxidant, antifungal, hypoglycemic
Quinones
Naphthoquinones, Naphthodiantrones, Anthraquinones & Kavalactones
Ubiquinol (Q10), menaquinone (vit K), plastoquinone, phylloquinone
Juglone, lapachol, plumbagone, shikonin, hypericin, sennosides, carmine, fagopyrin, emodins, rhein, kavain, yangonin, methysticin
Anti-tumoral, anti-leukemic, antimicrobial, antiparasitic, antifungal, antiviral, anti-inflammatory, cardioprotective, laxative, hypnotic, sedative, anesthetic
Flavonoids
FlavonesApigenin, luteolin, baicalein
IsoflavonesGenistein, diadzein, biochanin
FlavononesNaringenin, eriodictyol, hesperetin, liquiritinAntioxidant, anti-tumoral, anti-microbial, antiviral, anti-atheromatous, anti-hypertensive, anti-inflammatory, hepatoprotective, endothelial protection, cardioprotective, neuroprotective, chemoprotective, immunoprotective, estrogen-mediated responses, anti-aging
FlavonolsQuercetin, kaempferol, myricetin, isorhamnetin
FlavanolsCatechin, epicatechin
Flavan-3-ol (OPC)1Epicatechin-3-gallate, epigallocatechin-3-gallate
AnthocyanidinsMalvadin, cyanidin, delphinidin, europinidin, pelargonidin, peonidin, rosinidin, aurantinidin
Tannins
Gallo- & Ellagitannins
Condensed tannins (Proanthocyanidins)
Galloyl derivatives, ellagic acid, punicalagin, rugosin-D, oenthein-B, sanguiin, geraniin, agrimoniin, puncialin, corilagin
Procyanidins (OPC), propelargonidins, prodelphinidins, profisetinidins, proteracacinidins, theaflavins
Anti-tumoral, anti-inflammatory, antioxidant, antidiarrhoeic, anti-hemorrhagic, antimicrobial, hypolipidaemic, astringent, sclerosis, cardioprotective, endothelial function, platelet function, anti-hypertensive, anti-atherosclerotic, oral health
1 OPC—oligomeric procyanidins.
Table 2. Natural functional ingredients and potential benefits: Terpenes and terpenoids.
Table 2. Natural functional ingredients and potential benefits: Terpenes and terpenoids.
Chemical Category/ClassChemical Name/SubclassExample of CompoundsPotential Benefits
Monoterpenes/oids
(main constituent of essential oils)
Regular
Monocyclics
Acyclics
Bicyclics
Irregular
Iridoids
Pyrethrins
Cannabinoids
Limonene, terpineol, menthol, thymol, p-cymene, carvacrol
Linalool, citronelle, geranial
Camphor, α-pinene, thujone
Nepetalactone, valtrate, harpagide, oleuropein
Pyrethrin, chrysanthemic acid, cinerin, jazmolone
Δ9-tetrahydrocannabinol, cannabidiol, cannabicylol
Antifungal, antibacterial, antioxidant, anticancer, anti-spasmodic, analgesic, vasodilator, cardiovascular protector, anti-inflammatory, antidiabetic, anti-obesity, gut microbiota modulator, sedative, hepatoprotector, chloleretic, laxative, antiviral, insecticidal
Euphoriant, analgesic, neuroprotective, antiemetic, anxiolytic, anti-tumoral, anti-inflammatory, bronchodilator
Sesquiterpenes/oidsIn EOs
Lactones
Bisabolol and its oxides, matricin, chamazulene, gossypol, zingerbene
Germacrene, achillin, artemisin, cnicin, parthenolide, tanacetin, helenalin
Anti-inflammatory, wound-healing, contraceptive, anesthetic, antibacterial, antifungal, anti-protozoal, analgesic, anti-tumoral
Diterpenes/oidsAcyclic, mono-, bi-,
tri-, and tetracyclic
Forskolin, marrubiin, paclitaxel, andrographolide, ginkgolides, bilobide, stevioside, rebaudioside, abietic acid, hautriwaic acidAntihypertensive, vasodilatory, bronchodilatory, platelet aggregation inhibition, anti-tumoral, intraocular pressure regulator, hepatoprotector, immunomodulatory, neuroprotection, anti-diabetic, sweetener
Triterpenes/oidsFree Phytosterols
Limonoids
Lanosterol, ganosterol, lupeol
Sitosterol, campesterol, gugusterol, stigmasterol, brassicasterol, avenasterol, cycloartenol
Azadirachtin, limonin, nomilin
Blood cholesterol and LDL level regulator, hypocholesterolemic, hypolipidemic, anti-obesity, cardio-, neuro-, thyroid-protective, anti-tumoral
Antifeedant, insecticidal
Saponins
Non-steroidal
Steroidal
(so-called Cardenolides/Bufanolides, including some
cardiac glycosides *)
Glycyrrhicin, ginsenosides, jujubosides, asiatoside, betulin
Diosgenin, sarasapogenin, ruscogenins, withaferin-A
Digitoxin *, digoxin *, convallatoxin *, cimarin *, proscillaridin *
Many systemic effects: antiallergic, anti-tumoral, immunomodulatory, anti-(bacterial, fungal, viral), cardio-, hepato-, neuro-protective, hypoglycemic, estrogenic-, digestive-regulator, hypocholesterolaemic, hearth arrhythmia & failure *, angiogenesis inhibitor *, apoptotic *, autophagic *, neuroprotective *
Tetraterpenes/oidsCarotenes
Xanthophylls
Gukulenins
α-, β-, γ-, and δ-Carotene, lycopene, phytoene
Lutein, xanthins (viola-, luteo-, zea-, β-crypto-, astha-, anthera, cantha-), crocetins, and crocins
Gukulenin A and B
Antitumoral, pro-vitamin A, hypocholesterolemic, cardiovascular protection, neuroprotector, immunoactivator, skin protection
Antitumoral
MeroterpenesTerpenophenolsBakuchiol, ferruginol, totarol, epiconicolAntioxidant, antibacterial, anti-inflammatory, ocular protection
* indicates cardiac glycosides.
Table 3. Natural functional ingredients and potential benefits: Alkaloids and glucosinolates.
Table 3. Natural functional ingredients and potential benefits: Alkaloids and glucosinolates.
Chemical Category/ClassChemical Name/SubclassExample of CompoundsPotential Benefits
AlkaloidsFrom lysine
From ornithine
From tryptophan
From phenylalanine/tyrosine
Steroidal (alkaloid saponins)
Lupanine, cytosine, sedamine
Cocaine, hyoscyamine, nicotine
Vincamine, yohimbine, physostigmine, ergotamine, quinine, camptothecin
Ephedrine, berberine, emetine, morphine, capsaicin, eserpine, ergotamine, caffeine
Solanine, veratrine, solasodine
Analgesic, stimulant, narcotic, hyper-, hypotensive, bronchodilator, antimicrobial, anti-tumoral, vermicide, antimalarial, anticholinergic, cholagogue, emetic, cardiotonic, sympathetic, vasoconstrictor, antiasthmatic, anthelmintic
Glucosinolates & derivativesAliphatic
Aromatic
Indolic
Sulfur-derivatives
Glucoraphanin, sinigrin
Gluconasturtiin, glucotropaelin
Glucobrassicins
Isothiocyanates (allyl, benzyl), sulforaphane
Cancer prevention, anti-tumoral, antibacterial, antifungal, antioxidant, bronchodilator, skin irritation shooting
Table 4. Components of some useful essential oils as functional ingredients of different plants.
Table 4. Components of some useful essential oils as functional ingredients of different plants.
Common NameScientific NameCompounds *
AnisePimpinella anisumtrans-Anethole, γ-himachalene, estragole, 2-methyl-isoeugenol, anisaldehyde
BasilOcimum basilicumLinalool, 1,8-cineole, methyl eugenol, estragole, myrcene
BergamotCitrus bergamiaLimonene, linalyl acetate,γ-terpinene, linalool, β-pinene, β-bisabolene
CinnamonCinnamomum zeylanicumEugenol, β-caryophyllene, benzyl benzoate, cinnamyl acetate, α-phellandrene
Chinese tea treeMalaleuca alternifoliaTerpinen-4-ol, γ-terpinene, α-terpinene, 1,8-cineole, α-terpineol, p-cymene, terpinolene, α-pinene
CloveSyzygium aromaticumEugenol, β-caryophyllene, α-humulene, δ-cadinene
EucalyptEucalyptus globulus1,8-Cineole, α-pinene, limonene, p-cymene
FennelFoeniculum vulgareAnethole, fenchone, α-pinene, limonene, estragole, anisaldehyde, β-phellandrene
GingerZingiber officinaleGeranial, neral, geraniol, limonene
HypericumHypericum perforatumα-Pinene, β-caryophyllene, methyl-2-octane, dodecanol, myrcene
LavenderLavandula angustifoliaLinalyl acetate, linalool, terpinen-4-ol, ocimene, 1,8-cineole, limonene, camphor
LemongrassCymbopogon citratusGeranial, neral, geraniol, geranyl acetate, β-caryophyllene
MarjoramThymus mastichina1,8-Cineole, linalool, α-terpineol, α-pinene, limonene, linalyle acetate
PeppermintMentha piperitaMenthol, menthone, 1,8-cineole, menthylacetate, isomenthone, neomenthol, menthofurane, limonene, β-caryophyllene
RosemaryRosmarinus officinalisα-Thuyone, α-pinene, camphene, camphor, limonene, myrcene, borneol
SagebrushArtemisia vulgarisα-Thuyone, lyratol, 1,8-cineole, camphor, β-thuyone, artemisinin
SalviaSalvia officinalisα-Thuyone, camphor, 1,8-cineole, α-humulene, β-thuyone, α-pinene, bornyle acetate, limonene
SavorySatureja montanaCarvacrol,p-cymene, γ-terpinene, thymol
ThymeThymus vulgaris1,8-cineole, β-phellandrene, camphor, α-pinene, myrcene, borneol, limonene, neral
* In bold, the majority components.
Table 5. Some recent examples of EO use in dogs and its benefits.
Table 5. Some recent examples of EO use in dogs and its benefits.
Plant/EOs/Dose/App FormAnimalsBenefitsRefs.
Lavender/0.18 mL/inner pinnas of both earsBeagles↓ sympathovagal activity
↑ relax and calming
[51]
Artemisia absinthium
in vitro bioassay
Dogs↑ acaricidal activity
↓ egg and larvae of Rhipicephalus sanguineus dog tick
[52]
Menthol and thymol oils applied as gelAdult dogs↓ buccal halitosis[53]
Thymol and eugenol EOs
10 mL/kg, applied all over the skin and hair
English cocker spaniel dogs↓ larvae of Rhipicephalus sanguineus dog tick[54]
Turmeric oil at
2.5% in spray
Dogs with tick infestation↓ number of tick bites
In vitro effectivity:
turmeric > DEET > PMD
[55]
Otogen®, EOs (tea tree, thyme, sage, eucalyptus, rosemary, lavender), and vegetable oil (macadamia and sunflower)
7 days applied
Dogs of different breeds and ages↓ external otitis
↓ head shaking, erythema, and scraping
[56]
Thymol, cinnamaldehyde, and carvacrol; also clove and oregano EOs
In vitro assay
Dogs (bacterial and Malassezia pachydermatis isolates)↑ bactericidal and fungicidal activity
↑ Gram-positive bactericidal activity
↓ canine otitis
[57]
Dermoscent BIO BALM® Neem, rosemary, lavender, clove, tea tree, oregano, peppermint EOs, cedar bark extract, and PUFAs
Topical administration (0.6–2.4 mL weekly)
Dogs with low, medium, and severe atopic dermatitis↓ canine atopic dermatitis and pruritus score
↑ beneficial in ameliorating the clinical signs of atopic dermatitis
[58]
Dermoscent BIO BALM®
Topical administration
Dogs of different breeds↓ canine idiopathic noncomplicated nasal hyperkeratosis[59]
Dog food containing EOs (clove, rosemary, and oregano; also, vit. E) vs. synthetic antioxidant BHTDogs of different breeds and ages↓ lymphocytes, fecal bacterial count, oxidative stress (ROS),
↑ NPSH and glutathione S-transferases, feed conservation
[60]
Microencapsulated thymol, carvacrol, and cinnamaldehyde300 mg/kg of feedBeagle dogsneutrophils, lymphocytes, globulins, nitrogen oxide, GSH-POX
↓ ROS, fecal bacterial count, Salmonella, Escherichia coli
[44]
Cinnamon, thyme, clove, geranium, and tea tree EOs; also, eugenol, geraniol, cinnamaldehyde, thymol, and carvacrol individual components
In vitro assay
Dog and human skin fungal dermatosis↑ fungicidal activity, higher in dermatomycetes
↑ anti-mycosis therapy
[61]
Citrus, basilic, eucalyptus, cinnamon, lemon balm, lemongrass, lemon verbena, tea tree, savory, myrrh, and cannabis EOsPossible application to dogs with pyoderma↑ bactericidal activity against methicillin-resistant Staphylococcus
↑ pyoderma therapy
[62]
Vernonia brasiliana EO (Asteraceae)Antileishmanial activity against L. infantum promastigotes and cytotoxicity on canine DH82 cells↑ Antiparasitic effect, ROS, cell death by apoptosis
↓ mitochondrial membrane potential
Antagonistic interaction with miltefosine drug
[63]
Schinus molle EO (Anacardiaceae)Acaricidal effect on females and larval stages of R. sanguineusEO (2%) caused larval mortality (99.3%)
Inhibition of oviposition, egg hatching, and reproductive efficiency
[64]
Tagetes minuta EO (Asteraceae)Acaricidal effect in vitro and on dogs of R. sanguineus100% efficacy against larvae, nymphs, and adults of the tick on all tested conditions[65]
Thyme and oregano EOsBacterial and fungal isolates from canine otitis externaEOs showed good in vitro bactericidal and fungicidal activity against 100 isolates from dogs with otitis externa, including some highly drug-resistant isolates[50]
Cinnamon EOStaphylococcus strains from canine otitisEffective antimicrobial and antibiofilm activity
Potential alternative to treat ear infections in canines
[66]
↑ indicates increase activities, ↓ indicates decrease activities.
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Ruiz-Cano, D.; Sánchez-Carrasco, G.; El-Mihyaoui, A.; B. Arnao, M. Essential Oils and Melatonin as Functional Ingredients in Dogs. Animals 2022, 12, 2089. https://doi.org/10.3390/ani12162089

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Ruiz-Cano D, Sánchez-Carrasco G, El-Mihyaoui A, B. Arnao M. Essential Oils and Melatonin as Functional Ingredients in Dogs. Animals. 2022; 12(16):2089. https://doi.org/10.3390/ani12162089

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Ruiz-Cano, Domingo, Ginés Sánchez-Carrasco, Amina El-Mihyaoui, and Marino B. Arnao. 2022. "Essential Oils and Melatonin as Functional Ingredients in Dogs" Animals 12, no. 16: 2089. https://doi.org/10.3390/ani12162089

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