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Review

Health Benefits of Bioactive Compounds from the Genus Ilex, a Source of Traditional Caffeinated Beverages

by
Ren-You Gan
†,
Dan Zhang
†,
Min Wang
and
Harold Corke
*
Department of Food Science & Technology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China
*
Author to whom correspondence should be addressed.
†
These authors equally contributed to this paper.
Nutrients 2018, 10(11), 1682; https://doi.org/10.3390/nu10111682
Submission received: 10 October 2018 / Revised: 30 October 2018 / Accepted: 1 November 2018 / Published: 5 November 2018
(This article belongs to the Special Issue Tea in Health and Disease)
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Abstract

:
Tea and coffee are caffeinated beverages commonly consumed around the world in daily life. Tea from Camellia sinensis is widely available and is a good source of caffeine and other bioactive compounds (e.g., polyphenols and carotenoids). Other tea-like beverages, such as those from the genus Ilex, the large-leaved Kudingcha (Ilex latifolia Thunb and Ilex kudingcha C.J. Tseng), Yerba Mate (Ilex paraguariensis A. St.-Hil), Yaupon Holly (Ilex vomitoria), and Guayusa (Ilex guayusa Loes) are also traditional drinks, with lesser overall usage, but have attracted much recent attention and have been subjected to further study. This review summarizes the distribution, composition, and health benefits of caffeinated beverages from the genus Ilex. Plants of this genus mainly contain polyphenols and alkaloids, and show diverse health benefits, which, as well as supporting their further popularization as beverages, may also lead to potential applications in the pharmaceutical or nutraceutical industries.

1. Introduction

Caffeine (1,3,7-trimethylxanthine) is a member of a group of compounds known as purine alkaloids [1], occurs naturally in plants used to make beverages such as coffee and tea, and is added in the formulation of many soft drinks. Caffeine is a well-known central nervous system stimulant in humans. Tea from Camellia sinensis is the most popular non-alcoholic caffeine-containing beverage, and has a long consumption history all over the world. Major chemical constituents in tea are polyphenols, proteins, enzymes, caffeine, carbohydrates, and inorganics, which provide health beneficial properties [1,2]. However, caffeinated tea-like beverages with somewhat comparable chemical characteristics are also obtained from plants of the genus Ilex, mainly the large-leaved Kudingcha, Yerba Mate, Yaupon tea, and Guayusa tea, which have been well studied in recent years. The genus Ilex, comprising some 600 species, is widely distributed across most non-tropical parts of the world. The best-known species in Western literature is the European or English Holly, I. aquifolium L., with its characteristic red drupes (berries) and leaves widely used in Christmas decorations.
Kudingcha has a long consumption history in China and its commercial products are commonly found in the market. The large-leaved Kudingcha, including Ilex latifolia Thunb and Ilex kudingcha C.J. Tseng, have been reported to show significant medicinal or bioactive properties such as antioxidant, anti-inflammatory, anti-obesity, anti-cancer, modulation of gut microbiota, and antiproliferative effects [3,4,5,6,7,8,9,10]. In addition, Yerba Mate produced from leaves of the tree Ilex paraguariensis is a widely consumed beverage in South American countries such as Argentina, Brazil, Chile, Paraguay, and Uruguay, and the average annual consumption reaches around 3 kg to 10 kg per person. Yerba Mate tea has developed into a main alternative to coffee and black tea since it is characterized as having various health benefits, such as antimicrobial, antioxidant, anti-obesity, anti-diabetic, and cardiovascular protective effects [11,12,13,14,15,16,17,18]. Moreover, in the southeastern part of the United States, Yaupon tea (Yaupon Holly, Ilex vomitoria) is prepared as a healthy beverage by Native Americans [19]. The polyphenolics extracted from Yaupon Holly are free of catechin, and exhibit antioxidant, anti-inflammatory, and chemo-preventive effects [19,20,21]. Compared to green tea, processing and packaging have less effect on the degradation of polyphenolics in Yaupon Holly, indicating an advantage for commercial products of Yaupon tea. Guayusa tea, commercially known as Runa tea, is natively grown in the Amazon and has long been consumed by Amazonian indigenous tribes [22,23]. Ilex guayusa tea contains high levels of phenolic compounds, a good dietary resource with cellular antioxidant and anti-inflammatory properties [23,24].
Therefore, in order to provide a better understanding of Ilex-based caffeinated beverages, the relevant literature from the last ten years was searched in Web of Science. The geographical distributions of different Ilex species are summarized, followed by a discussion of their main bioactive compounds, and finally we highlight the potential health benefits and related molecular mechanisms. Since many Ilex species are already commonly consumed in the world, the information in this review will help to provide a scientific structure to explain the health benefits of Ilex-based beverages, which may encourage further development by the Ilex tea industry and lead to new products for the public.

2. Distribution

Plants of the genus Ilex are distributed widely in various parts of the world (Table 1). Large-leaved Kudingcha, an infusion made from evergreen trees of two species (I. kudingcha C.J. Tseng and I. latifolia Thunb.), is a popular bitter-tasting infused tea found in China and other Southeastern Asian countries (e.g., Singapore, Malaysia, and Vietnam) [3,25]. Yerba Mate tea, from a native South American holly shrub, is mainly produced and consumed in South America [26,27]. A study from Marcelo et al. reported that Yerba Mate could possibly be identified as to country of origin in South America by elemental concentration and chemometrics [28]. Leaves of Yaupon Holly (Ilex vomitoria), from an evergreen and caffeine-containing shrub native to the southeastern United States, was used to make a healthy beverage by Amerindians and later European colonists [19,29]. Guayusa is made from leaves of an evergreen tree native to South America and is grown in the Amazon. Guayusa has recently gained more attention [22,23].

3. Bioactive Compounds

Ilex genus plants are generally known to be rich in a wide variety of bioactive compounds, mainly polyphenols and alkaloids, which play an essential role in their health benefits.

3.1. Polyphenols

3.1.1. Polyphenols in Large-Leaved Kudingcha

Structurally, polyphenols are a class of compounds composed of benzene rings bonded to one or more hydroxyl groups. In previous published studies, different methods have been applied to determine the phenolic composition in Kudingcha. For example, the use of tyrosinase biosensor, Folin-Ciocalteu assay, high performance liquid chromatography (HPLC), HPLC-nuclear magnetic resonance (NMR), ultra-high performance liquid chromatography (UHPLC), UHPLC-diode array detector-linear ion trap-Orbitrap (UHPLC-DAD-LTQ-Orbitrap), liquid chromatography-photodiode array detector-atmospheric pressure chemical ionization-mass spectrometry (LC-PDA–APCI-MS), and the quantitative analysis of multiple components with a single marker (QAMS) methods were reported [3,24,25,30,37]. Using these methods, polyphenols can be identified and quantified effectively.
The total polyphenolic content (TPC) in I. latifolia was 188 mg gallic acid equivalent (GAE) per g dry plant material using the Folin–Ciocalteu method [10]. Caffeoylquinic acids (Figure 1) and their derivatives are the main polyphenols in Kudingcha. Compounds such as ethyl caffeate, 3,4-di-O-caffeoylquinic acid methyl ester, 3,5-di-O-caffeoylquinic acid methyl ester, and chlorogenic acid were identified in I. latifolia [38]. Chlorogenic acid (CGA), the ester of caffeic acid and quinic acid, is known for its biological functionality. The CGA derivatives 3-O-caffeoylquinic acid, 5-O-caffeoylquinic acid, 3,5-O-dicaffeoylquinic acid, and 4,5-O-dicaffeoylquinic acid have been identified as major compounds in methanol and ether acetate extracts of I. kudingcha [39]. This was confirmed by Che et al., who detected a total of 68 CGA candidates belonging to 12 categories [40]. Our previous study also reported that isomers of mono- and di-caffeoylquinic acids were the predominant compounds from Kudingcha genotypes of two Ilex species, and the average amount of major CGAs from these Kudingcha of different origins was 97 mg/g [25]. Furthermore, 18 active components including polyphenols, such as hydroxycasein, protocatechuic acid, rutin, neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, caffeic acid, and isochlorogenic acid, were first determined in I. kudingcha by the QAMS method, which was efficiently applied for simultaneous determination of different phenolic compounds [30]. Moreover, three caffeoylquinic acids, including neochlorogenic, chlorogenic, and cryptochlorogenic acids, and three dicaffeoylquinic acids, were identified as the main constituents in I. kudingcha [37].

3.1.2. Polyphenols in Yerba Mate

Polyphenols have been extracted from different parts of Yerba Mate, such as the whole plant, leaves, and stems. Of these, the highest level of phenolic compounds was found in the leaf extract [15]. From chromatographic analyses, the TPC was determined as about 51 mg/g dry mass (DM) in I. paraguariensis [41]. Moreover, determination of the TPC in Yerba Mate was performed by the Folin-Ciocalteu method, where 111 samples from the Parana State in Brazil were characterized [18]. Additionally, 46 different polyphenols from four commercial Yerba Mate products have been quantified, with hydroxycinnamic acid derivatives and flavonols accounting for 90% and 10% of the polyphenols present. Of these, 3-caffeoylquinic (26.8% to 28.8%), 5-caffeoylquinic (21.1% to 22.4%), 4-caffeoylquinic (12.6% to 14.2%), and 3,5-dicaffeoylquinic acids (9.5% to 11.3%) along with rutin (7.1% to 7.8%) were found to be the predominant polyphenolic compounds. In conclusion, I. paraguariensis was shown to be a good source of polyphenols [18,27]. Moreover, the content of lutein in aqueous extracts of Yerba Mate varied in different commercial samples, giving further prospects for a role in risk reduction for certain diseases [42].

3.1.3. Polyphenols in Yaupon Holly

Recently, limited research has been carried out on Yaupon Holly (I. vomitoria). In infusions, eight polyphenolic compounds were identified including mono-caffeoylquinic acids, di-caffeoylquinic acids, and two flavonol glycosides (quercetin 3-rutinosides and kaempferol 3-rutinoside), where the mono- and di-caffeoylquinic acids comprised 70% of the total polyphenolics [20]. Kim and Talcott also determined the composition of diverse polyphenolic compounds in tea infusion of Yaupon Holly, and found that 3-O-caffeoylquinic acid (chlorogenic acid), quercetin 3-rutinoside (rutin), 5-O-caffeoylquinic acid (neochlorogenic acid), and 4-O-caffeoylquinic acid (cryptochlorogenic acid) were the main phenolic compounds, with 423, 392, 318, and 125 mg/L rutin equivalents, respectively [21].

3.1.4. Polyphenols in Guayusa

I. guayusa teas showed high polyphenolic content totaling between 54 and 67 mg GAE/g DM, and phenolic mono- and di-caffeoylquinic acid derivatives were the major compounds determined by mass spectrometry [23]. Moreover, determination of TPC by the Slinkard and Singleton method showed a very different content in green leaves and in processed Guayusa [22]. For green leaves, TPC was about 55 mg/g DM, with hydroxycinnamic acid derivatives as the major constituents. The levels of 5-O-CQA (chlorogenic acid), 3,5-Dicaffeoylquinic acid (isochlorogenic acid), and 3-O-CQA (neochlorogenic acid) were 24, 16, and 8 mg/g DM, respectively. Processing methods such as blanching and fermentation are important factors affecting the TPC in Guayusa [22]. Kapp et al. reported that catechin, epicatechin, epicatechin gallate, epigallocatechin, and epigallocatechin gallate (EGCG) were found in I. guayusa leaves [36]. Other research showed that the major constituents of phenolics were hydroxycinnamic acid, and chlorogenic acid was the main phenolic compound found in both young and old leaves of Guayusa [24].
Overall, caffeoylquinic acids and their derivatives are the main phenolic compounds in the genus Ilex, which are summarized in Table 2.

3.2. Alkaloids

3.2.1. Alkaloids in Large-Leaved Kudingcha

Alkaloids are a class of naturally occurring compounds that mostly contain basic nitrogen atoms, showing a wide range of physiological and pharmacological effects. Methylxanthines, mainly caffeine and theobromine (Figure 2), are the main alkaloids in large-leaved kudingcha. However, alkaloid content is relatively low. It was reported that the content of total methylxanthines was around 7% to 9%, of which caffeine accounted for 3% to 6%, while theobromines made up only 0.1% [1].

3.2.2. Alkaloids in Yerba Mate

Methylxanthines are alkaloids naturally present in Yerba Mate, mainly comprising caffeine and theobromine [18,27,31]. It was reported that near infrared spectroscopy analysis could be applied to predict the total methylxanthine content in Yerba Mate. The total amount of methylxanthine in 25 samples of Yerba Mate ranged from 3.69 to 12.7 mg/g, with concentrations of caffeine and theobromine as 0.001 to 10.1 and 0.02 to 5.03 mg/g, respectively [31]. To quantify theobromine and caffeine in I. paraguariensis extracts, quality by design (QbD) models and UHPLC were optimized and applied, and indicated good future potential for application of this methodology [32]. In another study of samples of Yerba Mate methylxanthines were quantified by HPLC–DAD, with caffeine consistently higher in content than theobromine. Overall, Yerba Mate, with the total methylxanthines ranging from 8.2 to 10.2 mg/g, can be regarded as a moderate source of these purine alkaloids [18].

3.2.3. Alkaloids in Yaupon Holly

To identify residues of caffeinated beverages, three xanthines theobromine, theophylline, and caffeine (Figure 2) are commonly used as standards. It was found that Yaupon beverages contained all three, but their concentrations were significantly different between wild and domesticated types [34]. Moreover, the caffeine content in dioecious Yaupon Holly was 0% to 1.91% of dry weight, with the level strongly affected by nitrogen fertilizer but not by gender [19,29]. In another study, caffeine was undetectable by HPLC in Yaupon Holly leaves [43].

3.2.4. Alkaloids in Guayusa

The tea of I. guayusa, prepared by steeping leaves in boiling water, is consumed by Amazonian families and has a high caffeine content [23]. Kapp et al. found that the extract of Guayusa contained several secondary metabolites, such as caffeine and theobromine, at 36 and 0.3 mg/mL, respectively [36]. Extracts from I. guayusa have also been shown to contain caffeine [23].

4. Health Benefits

Some of the physiological effects of caffeinated beverages from Ilex are potentially beneficial for human health (Figure 3). Here, we further discuss the actions and related mechanisms of these potential benefits from different Ilex species.

4.1. Antioxidant Activity

Consumption of herbal teas prepared from I. paraguariensis, I. vomitoria, I. kudingcha, and I. guayusa have been reported to exhibit high reducing power, 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging and lipid peroxidation inhibition activities, thus relieving oxidative damage [44]. Based on the in vitro ferric-reducing antioxidant power (FRAP) assay, one extracted alkaloid constituent from I. latifolia had high reducing power [5]. Our previous study also found that the methanol extracts of six Kudingcha genotypes of the genus Ilex had relatively high in vitro antioxidant activity based on different antioxidant assays [25]. I. guayusa tea aqueous extracts (1 g/mL) prepared by conventional means protected 70% to 80% Caco-2 cells from oxidative damage [23], and prevented lipid peroxidation and DNA oxidative damage induced by ultraviolet radiation [45]. Similar antioxidant ability was also found in vivo and in human studies. Pereira et al. found that giving a gavage of Mate tea (20 mg/kg BW/day) to female Wistar rats minimized oxidative stress induced by hormonal changes during perimenopause [46]. Moreover, the impaired endogenous antioxidant defense system in the host could also be recovered by these widely consumed non-alcoholic beverages. As reported, the long-term ingestion of Mate tea (1 L/day) contributed to the increase in ferric-reducing antioxidant potential in dyslipidemic subjects [44], as well as the increased glutathione (GSH) concentration and decreased serum lipid hydroperoxides (LOOH) levels in type 2 diabetic mellitus (T2DM) subjects [47]. In addition, the acute consumption of freeze concentrated Yerba Mate infusion (100 mL) also enhanced the activities of antioxidant enzymes in healthy individuals, including catalase (CAT, 28.7%), superoxide dismutase (SOD, 21.3%), and glutathione peroxidase (GPx, 9.6%) in blood samples [48].
It is widely accepted that the counteraction on oxidative stress is mainly attributable to the existing phenolic compounds, especially chlorogenic acids (like mono- and dicaffeoylquinic acids) as well as flavonols [49,50], since in vitro antioxidant capacity has been confirmed to be positively correlated with their concentrations [13,51]. In order to better retain the contents and stability of health-beneficial antioxidants in Ilex teas, more attention should be paid to the adjustment of industrial processing methods and the improvement of packaging methods [22,52].

4.2. Anti-Inflammatory Activity

The inflammatory response is usually accompanied by the activation of macrophages, neutrophils, and various released inflammatory cytokines, such as tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, -6, and -12, triggering histological damage to specific tissues. Reduction of the exudate concentration, reestablishment of the balance between pro- and anti-inflammatory cytokines (IL-4 and -10), and suppression of the pro-inflammatory enzyme activity are considered to be major therapeutic targets in inflammation treatment.
High anti-inflammatory effects were observed in RAW 264.7 cells treated with I. latifolia ethanol extract (50 μg/mL), coupled with reduced nitric oxide (NO) production, which could dilate small blood vessels and increase the infiltration of pro-inflammatory mediators [5,10]. Similarly, a 10% to 30% NO inhibition rate was also reported in I. guayusa aqueous extracts (1 g/mL) treatment [23]. In addition, several animal experiments also reported the anti-inflammatory effects of these tea-like beverages. For instance, I. kudingcha C. J. Tseng methanol extracts (KME) administration upregulated the mRNA expression of inducible nitric oxide synthase (iNOS) and reduced the formation of pro-inflammatory factors like TNF-α, IL-1β, and IL-6 in dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) mice [53]. Besides, I. paraguariensis has been reported to show anti-inflammatory effects in various animal models, such as pleurisy in mice [54], cigarette smoke-induced acute lung inflammation in mice [55], obesity-related inflammation in rats [56,57], azoxymethane-induced inflammation in a rat colon [58], and acute edema in a mouse model [59] at concentrations ranging from 150 mg/kg to 250 mg/kg. The anti-inflammatory mechanism of Yerba Mate was reported to inhibit the NF-κB signaling pathway through restraining the phosphorylation of upstream IκB-α and GSK-3β, leading to blocking downstream iNOS and cyclooxygenase-2 (COX-2) expression, and the secretion of inflammatory cytokines [56,58]. However, the anti-inflammatory effects observed in several animal models have not been reported in human studies. Preliminary evidence has shown that Yerba Mate consumption (3 g Yerba Mate diluted in 200 mL water once a day for sixty days) did not alter the inflammatory parameters like high-sensitivity C-reactive protein (hs-CRP), fibrinogen, and HDL-C levels in 92 HIV/AIDS-positive individuals. The discrepancy between basic research and clinical cases could be due to the amount of beverage offered, the concentration of bioactive compounds in Mate tea, and the metabolic conditions of specific populations [60].

4.3. Antibacterial Activity

Compared to tea from Camellia sinensis, research on the antibacterial properties of Yerba Mate is relatively limited [27]. The antibacterial effects of Yerba Mate have been reported for Escherichia (E.) coli, Salmonella typhimurium, Listeria monocytogenes, Staphylococcus (S.) aureus, and even methicillin-resistant S. aureus (MRSA), with the antibacterial concentration ranging from 40 μg/mL to 7.4 mg/mL, and the inhibitory effects seemingly better on gram-positive bacteria than gram-negative bacteria [61]. Commonly, higher concentrations are required when applied to food systems due to the interaction of antibacterial substances with food components like proteins and lipids. Burris et al. found that the concentration of lyophilized aqueous extract of Yerba Mate in apple juice (40 mg/mL) was eight-fold higher than that in a medium (5 mg/mL) for equivalent bacterial inactivation [62]. A similar conclusion was also reached for ground beef, where the anti-MRSA concentration of Mate tea increased dose-dependently with increase of fat content [63].
Although the composition of Yerba Mate extract is relatively clear, conflicting results are shown with regards to the identification of bioactive compounds responsible for antimicrobial activity. Apart from the generally believed phenolic compounds [64], 3,4-dihydroxybenzaldehyde could significantly inhibit MRSA growth even at the lowest concentration of 100 μg/mL [65]. Besides, macromolecules like protein, occupying about 26% of Yerba Mate, might be responsible for the antibacterial activity since dialyzed aqueous extracts have also shown inhibitory effects on E. coli and S. aureus [62]. The antibacterial mechanism has been much less investigated, and it was pointed out that the tea extract of I. paraguariensis had a destructive effect on the central carbon metabolism and energy production pathways, as well as cell membrane integrity [66]. Overall, it is still unclear whether the ingredients that have important antibacterial properties are completely identified and whether they have synergistic or additive antibacterial effects.

4.4. Lipid-Reducing Activity

Several in vitro, in vivo, and human studies have reported the lipid-lowering benefits of the extract of I. paraguariensis. The inhibited accumulation of triglycerides in HepG2 cells and attenuated blood lipid levels were demonstrated in I. latifolia aqueous extracts [7,67]. Besides, N-butanolic fraction (n-BFIP), a standardized fraction rich in phenolic compounds derived from Yerba Mate was also shown to reduce triglycerides (TG) and low-density lipoprotein cholesterol (LDL-C) in high-fat-diet induced (HFD) rats by 30% and 26%, respectively [68]. This was consistent with the conclusion that polyphenols and methylxanthines in Yerba Mate showed higher lipid-reducing activity than saponins [69]. In addition, the lipid-reducing effect of Yerba Mate extract was proven to be effective not only in animal models, such as hyperlipidemic hamster model [70], rats [68], and rabbits [69], but also in humans. Dyslipidemic and normolipidemic subjects supplemented with 50 g (330 mL infusion and 3 times/day) Yerba Mate had about 10% reduction in lipid parameters (LDL-C and TG) [71,72]. In addition, it was reported that heavy drinkers of I. paraguariensis beverage (>1 L/day) had lower total cholesterol, LDL-C, and fasting glucose, but interestingly, their body weight was higher, compared with moderate drinkers [73]. This low-lipids high-body-weight paradox observed in the population of heavy drinkers of I. paraguariensis beverages could be due to the induced hypoglycemia and compensatory higher intake of refined carbohydrates, since their consumption of carbohydrates was higher than moderate drinkers [73].
For the lipid-reducing molecular mechanism, triterpenoid saponins (200 mg/kg/day) derived from I. latifolia was reported to lower lipids by the inhibition of sterol regulatory element-binding proteins (SREBPs) via enhancing AMP-activated protein kinase (AMPK) phosphorylation in a non-alcoholic fatty liver disease mouse model [74,75]. In addition, Yerba Mate aqueous extract was reported to improve plasma lipid profile both in vitro (3T3-L1 cells model) and in vivo (mice model), probably by inhibiting adipogenesis via downregulating the expression of adipogenesis related genes (Creb-1 and C/EBPα) [76].

4.5. Regulation of Gut Microbiota

More recently, growing attention has been paid to the effect of tea beverages on gut microbiota. Enhanced probiotic colonization was observed in a broiler chicken model fed with ground Yerba Mate leaf supplement (0.55% inclusion rate) [77]. Moreover, Ilex kudingcha extract (400 mg/kg) was demonstrated to change the diet-disrupted gut microbiota composition to normal state and increase their diversity in HFD-fed mice [78]. It was reported that polyphenols from I. latifolia played a critical role in establishing the structure of gut microbiota, since dietary polyphenols, especially dicaffeoylquinic acids (diCQAs), exhibited low bioavailability in the upper digestive tract, and reached the colon with an intact form and interacted with the colonic microbiota, contributing to the amelioration of the intestinal flora [79]. In addition, Xie et al. reported that diCQAs from Kudingcha enhanced the diversity of intestinal microbiota in vitro and promoted the generation of short-chain fatty acids (SCFAs) through gut microbiota, which in turn provided nutrients and energy for the optimization of gut microbial profile [9]. Therefore, the interaction between tea consumption and intestinal microbes can further improve the microbial colonization and promote human health.

4.6. Anti-Cancer Activity

Although epidemiological studies have reported a correlation between Mate tea consumption and esophageal cancer, it is most likely due to confounding factors, such as high consumption temperature rather than the carcinogenic constituents present [80,81], since any beverages with temperature above 65 °C are “likely carcinogenic to humans” [82]. In fact, the cytotoxic action against diverse cancer cells, such as breast cancer, oral cancer, nasopharyngeal carcinoma, and colon adenocarcinoma cells, was reported in Yaupon Holly leaves [20], Kudingcha extracts [5], and Yerba Mate extracts [83,84], which were tested with concentrations ranging from 10 μg/mL to 1000 μg/mL, and could not only inhibit the viability and proliferation of cancer cells, but also prevent metastasis and promote apoptosis of cancer cells. The presence of characteristic ingredients, mainly chlorogenic acid derivatives, may be responsible for the anti-cancer effects of Ilex Kudingcha [39].
Several studies also elucidated the anti-cancer molecular mechanisms. It was reported that caffeoylquinic acids in Ilex tea extracts were able to activate the pro-apoptotic factors caspase-3 and caspase-9 in TCA8113 cancer cells, and caspase-8 and caspase-3 in HT-29 human colon cancer cells, accompanied with the decreased expression of the inflammatory mediator NF-κB, which regulates cell proliferation, anti-apoptosis, and cell metastasis [6,85]. Overall, induction of cancer cell apoptosis and suppression of chronic inflammation could be two main mechanisms of the anti-cancer activity of Ilex tea.

4.7. Cardiovascular Protective Activity

Research on cardiovascular protection is limited, and only reported for I. paraguariensis and I. kudingcha. Kudingcha extract showed ameliorative effects on blood vessel contractility and blood flow in both rats and rabbits [3]. Kudingcha polysaccharides were also reported to have a protective effect against vascular dysfunction in high fructose-fed mice [86]. Yerba Mate consumption had great potential for reducing intermediate factors for cardiovascular diseases in both animal and human interventional studies [87]. In addition, improved blood viscosity and microcirculation were observed in 142 subjects supplemented with Yerba Mate tea (5 g/day) [88]. Moreover, reduced cardiovascular diseases were observed in 95 postmenopausal women consuming more than 1 L/day of mate infusion [89]. Thus, Ilex tea has great potential to be used as a preventive or therapeutic ingredient against cardiovascular diseases.

4.8. Anti-Obesity Activity

In recent years, reports have shown that caffeinated beverages from the genus Ilex, including Yerba Mate and Kudingcha, can reduce body weight and have great potential to be developed into anti-obesity drugs [78]. I. latifolia (0.33% aqueous extract was added to the HFD) showed protective effects against HFD-induced body weight gain in mice, accompanied by decreased adipocyte lipid accumulation and suppressed expression of lipogenic genes in the liver [90]. Furthermore, adipocyte size, adipocyte differentiation, and fat accumulation were also suppressed in obese rats after treatment with I. paraguariensis aqueous solution [91,92,93,94]. In addition to direct impact on adipogenesis, the anti-obesity effects of Mate extract were correlated with decreased appetite [95]. Hussein et al. found that chronic administration of Yerba Mate (50 mg/kg) induced elevated levels of the satiety markers glucagon-like peptide 1 (GLP-1) and leptin in high-fat diet-fed mice, leading to appetite-suppression and reduced food intake, thus decreasing body weight (BW) and body mass index [96].
Besides, the anti-obesity activity of Yerba Mate beverages has been validated in clinical trials. A randomized double-blind trial conducted by Kim et al. showed that body fat mass was significantly reduced in obese subjects supplemented with oral Yerba Mate capsules (3 g/day) for twelve weeks [97]. In addition, acute intake of Yerba Mate was confirmed to augment energy expenditure in healthy people [98], and it was interesting that a higher increase in energy expenditure could be induced by ingesting Yerba Mate at cold temperatures (e.g., 3 °C) rather than hot temperatures (e.g., 55 °C), without exerting negative impacts on the cardiovascular system [99]. Thus Yerba Mate appears to have great potential to be developed into an anti-obesity functional food.

4.9. Anti-Diabetic Activity

Increasing in vitro and in vivo studies support I. latifolia as an effective way to control postprandial hyperglycemia. Kudingcha aqueous extracts (6 mg/mL) could decrease 36% and 50% of the Na+-dependent and Na+-independent glucose absorption by Caco-2 cells in vitro, respectively [100]. In addition, blood glucose levels in the epinephrine hyperglycemia rat models also returned to normal levels under treatment with 5 or 10 g/kg Kudingcha extracts [3]. This result was in agreement with another in vivo study that oral administration of Yerba Mate (100 mg/kg) aqueous extract for seven weeks decreased blood glucose levels and improved insulin sensitivity in Tsumura Suzuki obese diabetic (TSOD) mice, thus reducing the risk of hyperglycemia [97]. The caffeoylquinic acid (CQA) derivatives derived from I. latifolia were further confirmed to play an important role in producing these effects, by means of binding to α-glucosidase via stable hydrogen bonding and hydrophobic interaction, thus reducing blood sugar levels [8]. In addition, clinical trials demonstrated the possibility of I. paraguariensis beverages for the prevention of diabetes complication, since long-term I. paraguariensis consumption (1 L/day, sixty days) improved glycemic profile and pre-diabetes related conditions (oxidative stress and dyslipidemia) in T2DM and pre-diabetic individuals [47]. Therefore, the consumption of herbal teas prepared from Ilex species is likely to be beneficial for the treatment of diabetes.

4.10. Neuroprotective Activity

The caffeinated beverages from the genus Ilex also show neuroprotective activity [101]. For instance, the exposure of cortical neurons to I. latifolia (1–100 μg/mL) was reported to inhibit neuronal death induced by glutamate, hypoxia, and amyloid β protein (Aβ) through suppressing the pathway of apoptosis [102,103]. Additionally, in vivo experiments also demonstrated that I. latifolia supplement (25 to 200 mg/kg) significantly inhibited Aβ (25–35)-induced memory impairment in mice and ischemia-induced neurological deficits in rats in a dose-dependent manner [103,104]. Clinical results further revealed its potential to inhibit the development of Parkinson’s disease [105].

4.11. Other Health Benefits

In addition to the health benefits mentioned above, Yerba Mate was also reported to improve bone mineral density in postmenopausal women and accelerated the healing of the alveolar socket in rats after tooth extraction [106,107]

5. Conclusions

In conclusion, this review summarized the distribution and chemical composition of the caffeinated beverages from the genus Ilex, including the large-leaved Kudingcha, Yerba Mate, Yaupon Holly, and Guayusa, along with their potential health benefits, including antioxidant, anti-inflammatory, antibacterial, lipid-reducing, regulation of gut microbiota, anti-cancer, cardiovascular protective, anti-obesity, anti-diabetic, neuroprotection, etc. However, the genus Ilex contains about 600 species, most of which still lack detailed investigation. In the future, intensive bioprospecting of the whole range of genetic resources is sure to reveal interesting and useful new compounds and new sources of high levels of known compounds. In addition, further research should aim at designing controlled clinical trials to investigate the effects of long-term consumption of well-characterized Ilex-based beverages on human health.

Author Contributions

Conceptualization, R.-Y.G. and H.C.; writing—original draft preparation, D.Z. and M.W.; writing—review and editing, R.-Y.G. and H.C.; supervision, H.C.; funding acquisition, R.-Y.G. and H.C.

Funding

This study was supported by the National Key R&D Program of China (2017YFC1600100), the Shanghai Pujiang Talent Plan (No. 18PJ1404600), the Shanghai Basic and Key Program (No. 18JC1410800), and the Shanghai Agricultural Science and Technology Key Program (18391900600).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Mohanpuria, P.; Kumar, V.; Yadav, S.K. Tea caffeine: Metabolism, functions, and reduction strategies. Food Sci. Biotechnol. 2010, 19, 275–287. [Google Scholar] [CrossRef]
  2. Zhang, C.; Suen, C.L.C.; Yang, C.; Quek, S.Y. Antioxidant capacity and major polyphenol composition of teas as affected by geographical location, plantation elevation and leaf grade. Food Chem. 2018, 244, 109–119. [Google Scholar] [CrossRef] [PubMed]
  3. Li, L.; Xu, L.J.; Ma, G.Z.; Dong, Y.M.; Peng, Y.; Xiao, P.G. The large-leaved kudingcha (Ilex latifolia thunb and Ilex kudingcha C.J. Tseng): A traditional Chinese tea with plentiful secondary metabolites and potential biological activities. J. Nat. Med. 2013, 67, 425–437. [Google Scholar] [CrossRef] [PubMed]
  4. Fan, J.L.; Wu, Z.W.; Zhao, T.H.; Sun, Y.; Ye, H.; Xu, R.J.; Zeng, X.X. Characterization, antioxidant and hepatoprotective activities of polysaccharides from Ilex latifolia Thunb. Carbohyd. Polym. 2014, 101, 990–997. [Google Scholar] [CrossRef] [PubMed]
  5. Hu, T.; He, X.W.; Jiang, J.G. Functional analyses on antioxidant, anti-inflammatory, and antiproliferative effects of extracts and compounds from Ilex latifolia thunb., a Chinese bitter tea. J. Agric. Food Chem. 2014, 62, 8608–8615. [Google Scholar] [CrossRef] [PubMed]
  6. Zhu, K.; Li, G.; Sun, P.; Wang, R.; Qian, Y.; Zhao, X. In vitro and in vivo anti-cancer activities of kuding tea (Ilex kudingcha C.J. Tseng) against oral cancer. Exp. Ther. Med. 2014, 7, 709–715. [Google Scholar] [CrossRef] [PubMed]
  7. Wang, C.Q.; Li, M.M.; Zhang, W.; Wang, L.; Fan, C.L.; Feng, R.B.; Zhang, X.Q.; Ye, W.C. Four new triterpenes and triterpene glycosides from the leaves of Ilex latifolia and their inhibitory activity on triglyceride accumulation. Fitoterapia 2015, 106, 141–146. [Google Scholar] [CrossRef] [PubMed]
  8. Xu, D.; Wang, Q.; Zhang, W.; Hu, B.; Zhou, L.; Zeng, X.; Sun, Y. Inhibitory activities of caffeoylquinic acid derivatives from Ilex kudingcha C.J. Tseng on α-glucosidase from Saccharomyces cerevisiae. J. Agric. Food Chem. 2015, 63, 3694–3703. [Google Scholar] [CrossRef] [PubMed]
  9. Xie, M.; Chen, G.; Wan, P.; Dai, Z.; Hu, B.; Chen, L.; Ou, S.; Zeng, X.; Sun, Y. Modulating effects of dicaffeoylquinic acids from Ilex kudingcha on intestinal microecology in vitro. J. Agric. Food Chem. 2017, 65, 10185–10196. [Google Scholar] [CrossRef] [PubMed]
  10. Zhang, T.-T.; Hu, T.; Jiang, J.-G.; Zhao, J.-W.; Zhu, W. Antioxidant and anti-inflammatory effects of polyphenols extracted from Ilex latifolia thunb. RSC Adv. 2018, 8, 7134–7141. [Google Scholar] [CrossRef]
  11. Burris, K.P.; Davidson, P.M.; Stewart, C.N., Jr.; Zivanovic, S.; Harte, F.M. Aqueous extracts of yerba mate (Ilex paraguariensis) as a natural antimicrobial against Escherichia coli O157:H7 in a microbiological medium and pH 6.0 apple juice. J. Food Prot. 2012, 75, 753–757. [Google Scholar] [CrossRef] [PubMed]
  12. Bassani, D.C.; Nunes, D.S.; Granato, D. Optimization of phenolics and flavonoids extraction conditions and antioxidant activity of roasted yerba-mate leaves (Ilex paraguariensis a. St.-Hil., aquifoliaceae) using response surface methodology. An. Acad. Bras. Cienc. 2014, 86, 923–933. [Google Scholar] [CrossRef]
  13. Molin, R.F.; Dartora, N.; Borges, A.C.P.; Gonçalves, I.L.; Di Luccio, M.; Valduga, A.T. Total phenolic contents and antioxidant activity in oxidized leaves of mate (Ilex paraguariensis St. Hil). Braz. Arch. Biol. Technol. 2014, 57, 997–1003. [Google Scholar] [CrossRef]
  14. Boado, L.S.; Fretes, R.M.; Brumovsky, L.A. Bioavailability and antioxidant effect of the Ilex paraguariensis polyphenols. Nutr. Food Sci. 2015, 45, 326–335. [Google Scholar] [CrossRef]
  15. Souza, A.H.P.; Correa, R.C.G.; Barros, L.; Calhelha, R.C.; Santos-Buelga, C.; Peralta, R.M.; Bracht, A.; Matsushita, M.; Ferreira, I.C.F.R. Phytochemicals and bioactive properties of Ilex paraguariensis: An in-vitro comparative study between the whole plant, leaves and stems. Food Res. Int. 2015, 78, 286–294. [Google Scholar] [CrossRef] [PubMed]
  16. Colpo, A.C.; de Lima, M.E.; Maya-Lopez, M.; Rosa, H.; Marquez-Curiel, C.; Galvan-Arzate, S.; Santamaria, A.; Folmer, V. Compounds from Ilex paraguariensis extracts have antioxidant effects in the brains of rats subjected to chronic immobilization stress. Appl. Physiol. Nutr. Metab. 2017, 42, 1172–1178. [Google Scholar] [CrossRef] [PubMed]
  17. Konieczynski, P.; Viapiana, A.; Wesolowski, M. Comparison of infusions from black and green teas (Camellia sinensis l. Kuntze) and erva-mate (Ilex paraguariensis a. St.-Hil.) based on the content of essential elements, secondary metabolites, and antioxidant activity. Food Anal. Method 2017, 10, 3063–3070. [Google Scholar] [CrossRef]
  18. Mateos, R.; Baeza, G.; Sarria, B.; Bravo, L. Improved LC-MSn characterization of hydroxycinnamic acid derivatives and flavonols in different commercial mate (Ilex paraguariensis) brands. Quantification of polyphenols, methylxanthines, and antioxidant activity. Food Chem. 2018, 241, 232–241. [Google Scholar] [CrossRef] [PubMed]
  19. Palumbo, M.J.; Talcott, S.T.; Putz, F.E. Ilex vomitoria ait. (yaupon): A native north American source of a caffeinated and antioxidant-rich tea. Econ. Bot. 2009, 63, 130–137. [Google Scholar] [CrossRef]
  20. Noratto, G.D.; Kim, Y.; Talcott, S.T.; Mertens-Talcott, S.U. Flavonol-rich fractions of yaupon holly leaves (Ilex vomitoria, aquifoliaceae) induce microRNA-146a and have anti-inflammatory and chemopreventive effects in intestinal myofribroblast CCD-18Co cells. Fitoterapia 2011, 82, 557–569. [Google Scholar] [CrossRef] [PubMed]
  21. Kim, Y.; Talcott, S.T. Tea creaming in nonfermented teas from Camellia sinensis and Ilex vomitoria. J. Agric. Food Chem. 2012, 60, 11793–11799. [Google Scholar] [CrossRef] [PubMed]
  22. Garcia-Ruiz, A.; Baenas, N.; Benitez-Gonzalez, A.M.; Stinco, C.M.; Melendez-Martinez, A.J.; Moreno, D.A.; Ruales, J. Guayusa (Ilex guayusa L.) new tea: Phenolic and carotenoid composition and antioxidant capacity. J. Sci. Food Agric. 2017, 97, 3929–3936. [Google Scholar] [CrossRef] [PubMed]
  23. Pardau, M.D.; Pereira, A.S.P.; Apostolides, Z.; Serem, J.C.; Bester, M.J. Antioxidant and anti-inflammatory properties of Ilex guayusa tea preparations: A comparison to Camellia sinensis teas. Food Funct. 2017, 8, 4601–4610. [Google Scholar] [CrossRef] [PubMed]
  24. Villacis-Chiriboga, J.; Garcia-Ruiz, A.; Baenas, N.; Moreno, D.A.; Melendez-Martinez, A.J.; Stinco, C.M.; Jerves-Andrade, L.; Leon-Tamariz, F.; Ortiz-Ulloa, J.; Ruales, J. Changes in phytochemical composition, bioactivity and in vitro digestibility of guayusa leaves (Ilex guayusa loes.) in different ripening stages. J. Sci. Food Agric. 2018, 98, 1927–1934. [Google Scholar] [CrossRef] [PubMed]
  25. Zhu, F.; Cai, Y.Z.; Sun, M.; Ke, J.X.; Lu, D.Y.; Corke, H. Comparison of major phenolic constituents and in vitro antioxidant activity of diverse kudingcha genotypes from Ilex kudingcha, Ilex cornuta, and Ligustrum robustum. J. Agric. Food Chem. 2009, 57, 6082–6089. [Google Scholar] [CrossRef] [PubMed]
  26. Heck, C.I.; De Mejia, E.G. Yerba mate tea (Ilex paraguariensis): A comprehensive review on chemistry, health implications, and technological considerations. J. Food Sci. 2007, 72, R138–R151. [Google Scholar] [CrossRef] [PubMed]
  27. Burris, K.P.; Harte, F.M.; Davidson, P.M.; Stewart, C.N.; Zivanovic, S. Composition and bioactive properties of yerba mate (Ilex paraguariensis a. St.-Hil.): A review. Chil. J. Agric. Res. 2012, 72, 268–274. [Google Scholar] [CrossRef]
  28. Marcelo, M.C.A.; Martins, C.A.; Pozebon, D.; Dressler, V.L.; Ferrao, M.F. Classification of yerba mate (Ilex paraguariensis) according to the country of origin based on element concentrations. Microchem. J. 2014, 117, 164–171. [Google Scholar] [CrossRef]
  29. Palumbo, M.J.; Putz, F.E.; Talcott, S.T. Nitrogen fertilizer and gender effects on the secondary metabolism of yaupon, a caffeine-containing north American holly. Oecologia 2007, 151, 1–9. [Google Scholar] [CrossRef] [PubMed]
  30. Yi, H.; Zhou, J.; Shang, X.Y.; Zhao, Z.X.; Peng, Q.; Zhu, M.J.; Zhu, C.C.; Lin, C.Z.; Liu, Q.D.; Liao, Q.F.; et al. Multi-component analysis of Ilex kudingcha C. J. Tseng by a single marker quantification method and chemometric discrimination of HPLC fingerprints. Molecules 2018, 23, 854. [Google Scholar] [CrossRef] [PubMed]
  31. Mazur, L.; Peralta-Zamora, P.G.; Demczuk, B.; Ribani, R.H. Application of multivariate calibration and NIR spectroscopy for the quantification of methylxanthines in yerba mate (Ilex paraguariensis). J. Food Compos. Anal. 2014, 35, 55–60. [Google Scholar] [CrossRef]
  32. Pinto, R.M.C.; Lemes, B.M.; Zielinski, A.A.F.; Klein, T.; de Paula, F.; Kist, A.; Marques, A.S.F.; Nogueira, A.; Demiate, I.M.; Beltrame, F.L. Detection and quantification of phytochemical markers of Ilex paraguariensis by liquid chromatography. Quim. Nova 2015, 38, 1219–1225. [Google Scholar] [CrossRef]
  33. Mateos, R.; Baeza, G.; Martinez-Lopez, S.; Sarria, B.; Bravo, L. LC-MSn characterization of saponins in mate (Ilex paraguariens, St. Hil) and their quantification by HPLC-DAD. J. Food Compos. Anal. 2017, 63, 164–170. [Google Scholar] [CrossRef]
  34. King, A.; Powis, T.G.; Cheong, K.F.; Gaikwad, N.W. Cautionary tales on the identification of caffeinated beverages in north America. J. Archaeol. Sci. 2017, 85, 30–40. [Google Scholar] [CrossRef]
  35. Duenas, J.F.; Jarrett, C.; Cummins, I.; Logan-Hines, E. Amazonian guayusa (Ilex guayusa Loes.): A historical and ethnobotanical overview. Econ. Bot. 2016, 70, 85–91. [Google Scholar] [CrossRef]
  36. Kapp, R.W.; Mendes, O.; Roy, S.; McQuate, R.S.; Kraska, R. General and genetic toxicology of guayusa concentrate (Ilex guayusa). Int. J. Toxicol. 2016, 35, 222–242. [Google Scholar] [CrossRef] [PubMed]
  37. Zhou, J.; Yi, H.; Zhao, Z.X.; Shang, X.Y.; Zhu, M.J.; Kuang, G.J.; Zhu, C.C.; Zhang, L. Simultaneous qualitative and quantitative evaluation of Ilex kudingcha C.J. Tseng by using UPLC and UHPLC-QTOE-MS/MS. J. Pharm. Biomed. 2018, 155, 15–26. [Google Scholar] [CrossRef] [PubMed]
  38. Hu, T.; He, X.W.; Jiang, J.G.; Xu, X.L. Efficacy evaluation of a Chinese bitter tea (Ilex latifolia thunb.) via analyses of its main components. Food Funct. 2014, 5, 876–881. [Google Scholar] [CrossRef] [PubMed]
  39. Zhong, T.; Piao, L.H.; Kim, H.J.; Liu, X.D.; Jiang, S.N.; Liu, G.M. Chlorogenic acid-enriched extract of Ilex kudingcha C.J. Tseng inhibits angiogenesis in zebrafish. J. Med. Food 2017, 20, 1160–1167. [Google Scholar] [CrossRef] [PubMed]
  40. Che, Y.Y.; Wang, Z.B.; Zhu, Z.Y.; Ma, Y.Y.; Zhang, Y.Q.; Gu, W.; Zhang, J.Y.; Rao, G.X. Simultaneous qualitation and quantitation of chlorogenic acids in kuding tea using ultra-high-performance liquid chromatography-diode array detection coupled with linear ion trap-orbitrap mass spectrometer. Molecules 2016, 21, 1728. [Google Scholar] [CrossRef] [PubMed]
  41. Zwyrzykowska, A.; Kupczynski, R.; Jarosz, B.; Szumny, A.; Kucharska, A.Z. Qualitative and quantitative analysis of polyphenolic compounds in Ilex sp. Open Chem. 2015, 13, 1303–1312. [Google Scholar] [CrossRef]
  42. da Silveira, T.F.F.; Meinhart, A.D.; Coutinho, J.P.; de Souza, T.C.L.; Cunha, E.C.E.; de Moraes, M.R.; Godoy, H.T. Content of lutein in aqueous extracts of yerba mate (Ilex paraguariensis St. Hil). Food Res. Int. 2016, 82, 165–171. [Google Scholar] [CrossRef]
  43. Kim, Y.; Welt, B.A.; Talcott, S.T. The impact of packaging materials on the antioxidant phytochemical stability of aqueous infusions of green tea (Camellia sinensis) and yaupon holly (Ilex vomitoria) during cold storage. J. Agric. Food Chem. 2011, 59, 4676–4683. [Google Scholar] [CrossRef] [PubMed]
  44. Boaventura, B.C.; Di Pietro, P.F.; Stefanuto, A.; Klein, G.A.; de Morais, E.C.; de Andrade, F.; Wazlawik, E.; da Silva, E.L. Association of mate tea (Ilex paraguariensis) intake and dietary intervention and effects on oxidative stress biomarkers of dyslipidemic subjects. Nutrition 2012, 28, 657–664. [Google Scholar] [CrossRef] [PubMed]
  45. Barg, M.; Rezin, G.T.; Leffa, D.D.; Balbinot, F.; Gomes, L.M.; Carvalho-Silva, M.; Vuolo, F.; Petronilho, F.; Dal-Pizzol, F.; Streck, E.L.; et al. Evaluation of the protective effect of Ilex paraguariensis and Camellia sinensis extracts on the prevention of oxidative damage caused by ultraviolet radiation. Environ. Toxicol. Pharmacol. 2014, 37, 195–201. [Google Scholar] [CrossRef] [PubMed]
  46. Pereira, A.A.F.; Tirapeli, K.G.; Chaves-Neto, A.H.; da Silva Brasilino, M.; da Rocha, C.Q.; Bello-Klein, A.; Llesuy, S.F.; Dornelles, R.C.M.; Nakamune, A. Ilex paraguariensis supplementation may be an effective nutritional approach to modulate oxidative stress during perimenopause. Exp. Gerontol. 2017, 90, 14–18. [Google Scholar] [CrossRef] [PubMed]
  47. Boaventura, B.C.B.; Di Pietro, P.F.; Klein, G.A.; Stefanuto, A.; de Morais, E.C.; de Andrade, F.; Wazlawik, E.; da Silva, E.L. Antioxidant potential of mate tea (Ilex paraguariensis) in type 2 diabetic mellitus and pre-diabetic individuals. J. Funct. Foods 2013, 5, 1057–1064. [Google Scholar] [CrossRef]
  48. Bremer Boaventura, B.C.; da Silva, E.L.; Liu, R.H.; Prudêncio, E.S.; Di Pietro, P.F.; Becker, A.M.; Amboni, R.D.d.M.C. Effect of yerba mate (Ilex paraguariensis a. St. Hil.) infusion obtained by freeze concentration technology on antioxidant status of healthy individuals. LWT Food Sci. Technol. 2015, 62, 948–954. [Google Scholar] [CrossRef]
  49. Baeza, G.; Sarria, B.; Mateos, R.; Bravo, L. Dihydrocaffeic acid, a major microbial metabolite of chlorogenic acids, shows similar protective effect than a yerba mate phenolic extract against oxidative stress in HepG2 cells. Food Res. Int. 2016, 87, 25–33. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Zhao, X.; Song, J.L.; Yi, R.; Li, G.; Sun, P.; Park, K.Y.; Suo, H. Comparison of antioxidative effects of insect tea and its raw tea (kuding tea) polyphenols in Kunming mice. Molecules 2018, 23, 204. [Google Scholar] [CrossRef] [PubMed]
  51. de Oliveira, C.C.; Calado, V.M.; Ares, G.; Granato, D. Statistical approaches to assess the association between phenolic compounds and the in vitro antioxidant activity of Camellia sinensis and Ilex paraguariensis teas. Crit. Rev. Food Sci. Nutr. 2015, 55, 1456–1473. [Google Scholar] [CrossRef] [PubMed]
  52. Yonny, M.E.; Medina, A.V.; Nazareno, M.A.; Chaillou, L.L. Enhancement in the oxidative stability of green peas by Ilex paraguariensis addition in a blanching process before their refrigerated and frozen storage. LWT 2018, 91, 315–321. [Google Scholar] [CrossRef]
  53. Song, J.L.; Qian, Y.; Li, G.J.; Zhao, X. Anti-inflammatory effects of kudingcha methanol extract (Ilex kudingcha c.J. Tseng) in dextran sulfate sodium-induced ulcerative colitis. Mol. Med. Rep. 2013, 8, 1256–1262. [Google Scholar] [CrossRef] [PubMed]
  54. Luz, A.B.G.; da Silva, C.H.B.; Nascimento, M.; de Campos Facchin, B.M.; Baratto, B.; Frode, T.S.; Reginatto, F.H.; Dalmarco, E.M. The anti-inflammatory effect of Ilex paraguariensis a. St. Hil (mate) in a murine model of pleurisy. Int. Immunopharmacol. 2016, 36, 165–172. [Google Scholar] [CrossRef] [PubMed]
  55. Lanzetti, M.; Bezerra, F.S.; Romana-Souza, B.; Brando-Lima, A.C.; Koatz, V.L.; Porto, L.C.; Valenca, S.S. Mate tea reduced acute lung inflammation in mice exposed to cigarette smoke. Nutrition 2008, 24, 375–381. [Google Scholar] [CrossRef] [PubMed]
  56. Pimentel, G.D.; Lira, F.S.; Rosa, J.C.; Caris, A.V.; Pinheiro, F.; Ribeiro, E.B.; Oller do Nascimento, C.M.; Oyama, L.M. Yerba mate extract (Ilex paraguariensis) attenuates both central and peripheral inflammatory effects of diet-induced obesity in rats. J. Nutr. Biochem. 2013, 24, 809–818. [Google Scholar] [CrossRef] [PubMed]
  57. Munoz-Culla, M.; Saenz-Cuesta, M.; Guereca-Barandiaran, M.J.; Ribeiro, M.L.; Otaegui, D. Yerba mate (Ilex paraguariensis) inhibits lymphocyte activation in vitro. Food Funct. 2016, 7, 4556–4563. [Google Scholar] [CrossRef] [PubMed]
  58. Puangpraphant, S.; Dia, V.P.; de Mejia, E.G.; Garcia, G.; Berhow, M.A.; Wallig, M.A. Yerba mate tea and mate saponins prevented azoxymethane-induced inflammation of rat colon through suppression of NF-κB p65ser(311) signaling via IκB-α and GSK-3β reduced phosphorylation. Biofactors 2013, 39, 430–440. [Google Scholar] [CrossRef] [PubMed]
  59. Schinella, G.; Neyret, E.; Console, G.; Tournier, H.; Prieto, J.M.; Rios, J.L.; Giner, R.M. An aqueous extract of Ilex paraguariensis reduces carrageenan-induced edema and inhibits the expression of cyclooxygenase-2 and inducible nitric oxide synthase in animal models of inflammation. Planta Med. 2014, 80, 961–968. [Google Scholar] [CrossRef] [PubMed]
  60. Petrilli, A.A.; Souza, S.J.; Teixeira, A.M.; Pontilho, P.M.; Souza, J.M.P.; Luzia, L.A.; Rondo, P.H.C. Effect of Chocolate and Yerba Mate Phenolic Compounds on Inflammatory and Oxidative Biomarkers in HIV/AIDS Individuals. Nutrients 2016, 8, 132. [Google Scholar] [CrossRef] [PubMed]
  61. Prado Martin, J.G.; Porto, E.; de Alencar, S.M.; da Glória, E.M.; Corrêa, C.B.; Ribeiro Cabral, I.S. Antimicrobial activity of yerba mate (Ilex paraguariensis St. Hil.) against food pathogens. Rev. Argent. Microbiol. 2013, 45, 93–98. [Google Scholar] [CrossRef]
  62. Burris, K.P.; Davidson, P.M.; Stewart, C.N., Jr.; Harte, F.M. Antimicrobial activity of yerba mate (Ilex paraguariensis) aqueous extracts against Escherichia coli O157:H7 and Staphylococcus aureus. J. Food Sci. 2011, 76, M456–M462. [Google Scholar] [CrossRef] [PubMed]
  63. Burris, K.P.; Higginbotham, K.L.; Stewart, C.N. Aqueous extracts of yerba mate as bactericidal agents against methicillin-resistant Staphylococcus aureus in a microbiological medium and ground beef mixtures. Food Control. 2015, 50, 748–753. [Google Scholar] [CrossRef]
  64. Correa, V.G.; Goncalves, G.A.; de Sa-Nakanishi, A.B.; Ferreira, I.; Barros, L.; Dias, M.I.; Koehnlein, E.A.; de Souza, C.G.M.; Bracht, A.; Peralta, R.M. Effects of in vitro digestion and in vitro colonic fermentation on stability and functional properties of yerba mate (Ilex paraguariensis a. St. Hil.) beverages. Food Chem. 2017, 237, 453–460. [Google Scholar] [CrossRef] [PubMed]
  65. Rempe, C.S.; Burris, K.P.; Woo, H.L.; Goodrich, B.; Gosnell, D.K.; Tschaplinski, T.J.; Stewart, C.N., Jr. Computational ranking of yerba mate small molecules based on their predicted contribution to antibacterial activity against methicillin-resistant Staphylococcus aureus. PLoS ONE 2015, 10, e0123925. [Google Scholar] [CrossRef] [PubMed]
  66. Rempe, C.S.; Lenaghan, S.C.; Burris, K.P.; Stewart, C.N. Metabolomic analysis of the mechanism of action of yerba mate aqueous extract on Salmonella enterica serovar Typhimurium. Metabolomics 2017, 13. [Google Scholar] [CrossRef]
  67. Song, C.; Yu, Q.; Li, X.; Jin, S.; Li, S.; Zhang, Y.; Jia, S.; Chen, C.; Xiang, Y.; Jiang, H. The hypolipidemic effect of total saponins from kuding tea in high-fat diet-induced hyperlipidemic mice and its composition characterized by UPLC-QTOF-MS/MS. J. Food Sci. 2016, 81, H1313–H1319. [Google Scholar] [CrossRef] [PubMed]
  68. Balzan, S.; Hernandes, A.; Reichert, C.L.; Donaduzzi, C.; Pires, V.A.; Gasparotto, A., Jr.; Cardozo, E.L., Jr. Lipid-lowering effects of standardized extracts of Ilex paraguariensis in high-fat-diet rats. Fitoterapia 2013, 86, 115–122. [Google Scholar] [CrossRef] [PubMed]
  69. de Resende, P.E.; Kaiser, S.; Pittol, V.; Hoefel, A.L.; D’Agostini Silva, R.; Vieira Marques, C.; Kucharski, L.C.; Ortega, G.G. Influence of crude extract and bioactive fractions of Ilex paraguariensis a. St. Hil. (yerba mate) on the Wistar rat lipid metabolism. J. Funct. Foods 2015, 15, 440–451. [Google Scholar] [CrossRef]
  70. Gao, H.; Long, Y.; Jiang, X.; Liu, Z.; Wang, D.; Zhao, Y.; Li, D.; Sun, B.L. Beneficial effects of yerba mate tea (Ilex paraguariensis) on hyperlipidemia in high-fat-fed hamsters. Exp. Gerontol. 2013, 48, 572–578. [Google Scholar] [CrossRef] [PubMed]
  71. de Morais, E.C.; Stefanuto, A.; Klein, G.A.; Boaventura, B.C.; de Andrade, F.; Wazlawik, E.; Di Pietro, P.F.; Maraschin, M.; da Silva, E.L. Consumption of yerba mate (Ilex paraguariensis) improves serum lipid parameters in healthy dyslipidemic subjects and provides an additional LDL-cholesterol reduction in individuals on statin therapy. J. Agric. Food Chem. 2009, 57, 8316–8324. [Google Scholar] [CrossRef] [PubMed]
  72. Messina, D.; Soto, C.; Mendez, A.; Corte, C.; Kemnitz, M.; Avena, V.; Del Balzo, D.; Perez Elizalde, R. Lipid—Lowering effect of mate tea intake in dyslipidemic subjects. Nutr. Hosp. 2015, 31, 2131–2139. [Google Scholar] [CrossRef] [PubMed]
  73. Chaves, G.; Britez, N.; Oviedo, G.; Gonzalez, G.; Italiano, C.; Blanes, M.; Sandoval, G.; Mereles, D. Heavy drinkers of Ilex paraguariensis beverages show lower lipid profiles but higher body weight. Phytother. Res. 2018, 32, 1030–1038. [Google Scholar] [CrossRef] [PubMed]
  74. Feng, R.B.; Fan, C.L.; Liu, Q.; Liu, Z.; Zhang, W.; Li, Y.L.; Tang, W.; Wang, Y.; Li, M.M.; Ye, W.C. Crude triterpenoid saponins from Ilex latifolia (Da Ye Dong Qing) ameliorate lipid accumulation by inhibiting SREBP expression via activation of AMPK in a non-alcoholic fatty liver disease model. Chin. Med. 2015, 10, 23. [Google Scholar] [CrossRef] [PubMed]
  75. Che, Y.Y.; Wang, Q.H.; Xiao, R.Y.; Zhang, J.Y.; Zhang, Y.Q.; Gu, W.; Rao, G.X.; Wang, C.F.; Kuang, H.X. Kudinoside-d, a triterpenoid saponin derived from Ilex kudingcha suppresses adipogenesis through modulation of the AMPK pathway in 3T3-L1 adipocytes. Fitoterapia 2018, 125, 208–216. [Google Scholar] [CrossRef] [PubMed]
  76. Arcari, D.P.; Santos, J.C.; Gambero, A.; Ribeiro, M.L. The in vitro and in vivo effects of yerba mate (Ilex paraguariensis) extract on adipogenesis. Food Chem. 2013, 141, 809–815. [Google Scholar] [CrossRef] [PubMed]
  77. Gonzalez-Gil, F.; Diaz-Sanchez, S.; Pendleton, S.; Andino, A.; Zhang, N.; Yard, C.; Crilly, N.; Harte, F.; Hanning, I. Yerba mate enhances probiotic bacteria growth in vitro but as a feed additive does not reduce Salmonella enteritidis colonization in vivo. Poult. Sci. 2014, 93, 434–440. [Google Scholar] [CrossRef] [PubMed]
  78. Chen, G.; Xie, M.; Dai, Z.; Wan, P.; Ye, H.; Zeng, X.; Sun, Y. Kudingcha and fuzhuan brick tea prevent obesity and modulate gut microbiota in high-fat diet fed mice. Mol. Nutr. Food Res. 2018, 62, e1700485. [Google Scholar] [CrossRef] [PubMed]
  79. Xie, M.; Chen, G.; Hu, B.; Zhou, L.; Ou, S.; Zeng, X.; Sun, Y. Hydrolysis of dicaffeoylquinic acids from Ilex kudingcha happens in the colon by intestinal microbiota. J. Agric. Food Chem. 2016, 64, 9624–9630. [Google Scholar] [CrossRef] [PubMed]
  80. Dasanayake, A.P.; Silverman, A.J.; Warnakulasuriya, S. Mate drinking and oral and oro-pharyngeal cancer: A systematic review and meta-analysis. Oral. Oncol. 2010, 46, 82–86. [Google Scholar] [CrossRef] [PubMed]
  81. Amigo-Benavent, M.; Wang, S.; Mateos, R.; Sarria, B.; Bravo, L. Antiproliferative and cytotoxic effects of green coffee and yerba mate extracts, their main hydroxycinnamic acids, methylxanthine and metabolites in different human cell lines. Food Chem. Toxicol. 2017, 106, 125–138. [Google Scholar] [CrossRef] [PubMed]
  82. Gomez-Juaristi, M.; Martinez-Lopez, S.; Sarria, B.; Bravo, L.; Mateos, R. Absorption and metabolism of yerba mate phenolic compounds in humans. Food Chem. 2018, 240, 1028–1038. [Google Scholar] [CrossRef] [PubMed]
  83. Murad, L.D.; Soares Nda, C.; Brand, C.; Monteiro, M.C.; Teodoro, A.J. Effects of caffeic and 5-caffeoylquinic acids on cell viability and cellular uptake in human colon adenocarcinoma cells. Nutr. Cancer 2015, 67, 532–542. [Google Scholar] [CrossRef] [PubMed]
  84. Ronco, A.L.; De Stefani, E.; Mendoza, B.; Deneo-Pellegrini, H.; Vazquez, A.; Abbona, E. Mate intake and risk of breast cancer in uruguay: A. case-control study. Asian Pac. J. Cancer Prev. 2016, 17, 1453–1461. [Google Scholar] [CrossRef] [PubMed]
  85. Puangpraphant, S.; Berhow, M.A.; Vermillion, K.; Potts, G.; Gonzalez de Mejia, E. Dicaffeoylquinic acids in yerba mate (Ilex paraguariensis St. Hilaire) inhibit NF-κB nucleus translocation in macrophages and induce apoptosis by activating caspases-8 and -3 in human colon cancer cells. Mol. Nutr. Food Res. 2011, 55, 1509–1522. [Google Scholar] [CrossRef] [PubMed]
  86. Zhai, X.; Ren, D.; Luo, Y.; Hu, Y.; Yang, X. Chemical characteristics of an Ilex kuding tea polysaccharide and its protective effects against high fructose-induced liver injury and vascular endothelial dysfunction in mice. Food Funct. 2017, 8, 2536–2547. [Google Scholar] [CrossRef] [PubMed]
  87. Cardozo Junior, E.L.; Morand, C. Interest of mate (Ilex paraguariensis a. St.-Hil.) as a new natural functional food to preserve human cardiovascular health—A review. J. Funct. Foods 2016, 21, 440–454. [Google Scholar] [CrossRef]
  88. Yu, S.; Yue, S.; Liu, Z.; Zhang, T.; Xiang, N.; Fu, H. Yerba mate (Ilex paraguariensis) improves microcirculation of volunteers with high blood viscosity: A. randomized, double-blind, placebo-controlled trial. Exp. Gerontol. 2015, 62, 14–22. [Google Scholar] [CrossRef] [PubMed]
  89. da Veiga, D.T.A.; Bringhenti, R.; Copes, R.; Tatsch, E.; Moresco, R.N.; Comim, F.V.; Premaor, M.O. Protective effect of yerba mate intake on the cardiovascular system: A post hoc analysis study in postmenopausal women. Braz. J. Med. Biol. Res. 2018, 51, e7253. [Google Scholar] [CrossRef] [PubMed]
  90. Wu, H.; Chen, Y.L.; Yu, Y.; Zang, J.; Wu, Y.; He, Z. Ilex latifolia thunb protects mice from HFD-induced body weight gain. Sci. Rep. 2017, 7, 14660. [Google Scholar] [CrossRef] [PubMed]
  91. Silva, R.D.; Bueno, A.L.; Gallon, C.W.; Gomes, L.F.; Kaiser, S.; Pavei, C.; Ortega, G.G.; Kucharski, L.C.; Jahn, M.P. The effect of aqueous extract of gross and commercial yerba mate (Ilex paraguariensis) on intra-abdominal and epididymal fat and glucose levels in male Wistar rats. Fitoterapia 2011, 82, 818–826. [Google Scholar] [CrossRef] [PubMed]
  92. Lima Nda, S.; Franco, J.G.; Peixoto-Silva, N.; Maia, L.A.; Kaezer, A.; Felzenszwalb, I.; de Oliveira, E.; de Moura, E.G.; Lisboa, P.C. Ilex paraguariensis (yerba mate) improves endocrine and metabolic disorders in obese rats primed by early weaning. Eur. J. Nutr. 2014, 53, 73–82. [Google Scholar] [CrossRef] [PubMed]
  93. Gambero, A.; Ribeiro, M.L. The positive effects of yerba mate (Ilex paraguariensis) in obesity. Nutrients 2015, 7, 730–750. [Google Scholar] [CrossRef] [PubMed]
  94. de Oliveira, E.; Lima, N.S.; Conceicao, E.P.S.; Peixoto-Silva, N.; Moura, E.G.; Lisboa, P.C. Treatment with Ilex paraguariensis (yerba mate) aqueous solution prevents hepatic redox imbalance, elevated triglycerides, and microsteatosis in overweight adult rats that were precociously weaned. Braz. J. Med. Biol. Res. 2018, 51, e7342. [Google Scholar] [CrossRef] [PubMed]
  95. Kang, Y.R.; Lee, H.Y.; Kim, J.H.; Moon, D.I.; Seo, M.Y.; Park, S.H.; Choi, K.H.; Kim, C.R.; Kim, S.H.; Oh, J.H.; et al. Anti-obesity and anti-diabetic effects of yerba mate (Ilex paraguariensis) in C57BL/6J mice fed a high-fat diet. Lab. Anim. Res. 2012, 28, 23–29. [Google Scholar] [CrossRef] [PubMed]
  96. Hussein, G.M.E.; Matsuda, H.; Nakamura, S.; Hamao, M.; Akiyama, T.; Tamura, K.; Yoshikawa, M. Mate tea (Ilex paraguariensis) promotes satiety and body weight lowering in mice: Involvement of glucagon-like peptide-1. Biol. Pharm. Bull. 2011, 34, 1849–1855. [Google Scholar] [CrossRef] [PubMed]
  97. Kim, S.Y.; Oh, M.R.; Kim, M.G.; Chae, H.J.; Chae, S.W. Anti-obesity effects of yerba mate (Ilex paraguariensis): A randomized, double-blind, placebo-controlled clinical trial. BMC Complement Altern. Med. 2015, 15, 338. [Google Scholar] [CrossRef] [PubMed]
  98. De Oliveira, E.P.; Torezan, G.A.; Goncalves, L.D.; Corrente, J.E.; McLellan, K.C.P.; Burini, R.C. Acute intake of yerba mate increases energy expenditure of health young men: A. pilot study. Rbone-Rev. Bras. Obes. 2016, 10, 242–249. [Google Scholar]
  99. Maufrais, C.; Sarafian, D.; Dulloo, A.; Montani, J.P. Cardiovascular and metabolic responses to the ingestion of caffeinated herbal tea: Drink it hot or cold? Front. Physiol. 2018, 9, 315. [Google Scholar] [CrossRef] [PubMed]
  100. Wang, Z.; Clifford, M.N.; Sharp, P. Analysis of chlorogenic acids in beverages prepared from Chinese health foods and investigation, in vitro, of effects on glucose absorption in cultured Caco-2 cells. Food Chem. 2008, 108, 369–373. [Google Scholar] [CrossRef]
  101. Riachi, L.G.; De Maria, C.A.B. Yerba mate: An overview of physiological effects in humans. J. Funct. Foods 2017, 38, 308–320. [Google Scholar] [CrossRef]
  102. Kim, J.Y.; Lee, H.K.; Hwang, B.Y.; Kim, S.; Yoo, J.K.; Seong, Y.H. Neuroprotection of Ilex latifolia and caffeoylquinic acid derivatives against excitotoxic and hypoxic damage of cultured rat cortical neurons. Arch. Pharm. Res. 2012, 35, 1115–1122. [Google Scholar] [CrossRef] [PubMed]
  103. Kim, J.Y.; Lee, H.K.; Jang, J.Y.; Yoo, J.K.; Seong, Y.H. Ilex latifolia prevents amyloid beta protein (25–35)-induced memory impairment by inhibiting apoptosis and tau phosphorylation in mice. J. Med. Food 2015, 18, 1317–1326. [Google Scholar] [CrossRef] [PubMed]
  104. Kim, J.Y.; Jeong, H.Y.; Lee, H.K.; Yoo, J.K.; Bae, K.; Seong, Y.H. Protective effect of Ilex latifolia, a major component of “kudingcha”, against transient focal ischemia-induced neuronal damage in rats. J. Ethnopharmacol. 2011, 133, 558–564. [Google Scholar] [CrossRef] [PubMed]
  105. Gatto, E.M.; Melcon, C.; Parisi, V.L.; Bartoloni, L.; Gonzalez, C.D. Inverse association between yerba mate consumption and idiopathic Parkinson’s disease. A case-control study. J. Neurol. Sci. 2015, 356, 163–167. [Google Scholar] [CrossRef] [PubMed]
  106. Conforti, A.S.; Gallo, M.E.; Saravi, F.D. Yerba mate (Ilex paraguariensis) consumption is associated with higher bone mineral density in postmenopausal women. Bone 2012, 50, 9–13. [Google Scholar] [CrossRef] [PubMed]
  107. Brasilino, M.D.S.; Stringhetta-Garcia, C.T.; Pereira, C.S.; Pereira, A.A.F.; Stringhetta, K.; Leopoldino, A.M.; Crivelini, M.M.; Ervolino, E.; Dornelles, R.C.M.; de Melo Stevanato Nakamune, A.C.; et al. Mate tea (Ilex paraguariensis) improves bone formation in the alveolar socket healing after tooth extraction in rats. Clin. Oral. Investig. 2018, 22, 1449–1461. [Google Scholar] [CrossRef] [PubMed]
Nutrients 10 01682 g001 550
Figure 1. The chemical structures of caffeoylquinic acids.
Figure 1. The chemical structures of caffeoylquinic acids.
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Figure 2. The chemical structures of main alkaloids in the genus Ilex.
Figure 2. The chemical structures of main alkaloids in the genus Ilex.
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Figure 3. The health benefits of caffeinated beverages from the genus Ilex.
Figure 3. The health benefits of caffeinated beverages from the genus Ilex.
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Table
Table 1. Distribution of the most commonly consumed species of the genus Ilex.
Table 1. Distribution of the most commonly consumed species of the genus Ilex.
Common NameSpeciesDistributionReferences
Large-leaved KudingchaI. kudingcha C.J. TsengChina: Guangxi; Guangdong; Hainan[3,25,30]
I. latifolia Thunb.China: Zhejiang; Jiangsu; Fujian; Anhui; Hainan[3,6,7,10]
Yerba MateIlex paraguariensis A. St.-HilSouth America: Argentina; Brazil; Paraguay; Uruguay[26,27,31,32,33]
Yaupon HollyIlex vomitoriaSoutheastern United States[19,21,29,34]
GuayusaIlex guayusa LoesSouth America: Argentina, Southern of Brazil, Paraguay and Uruguay[22,24,35,36]
Table
Table 2. Main phenolic compounds in the genus Ilex.
Table 2. Main phenolic compounds in the genus Ilex.
Tea NameSpeciesMain PolyphenolsReference
Large-leaved KudingchaIlex kudingcha C. J. TsengNeochlorogenic acid[30,37]
Chlorogenic acid
Cryptochlorogenic acid
Protocatechuic acid[37]
Caffeic acid
Isochlorogenic acid
Rutin
I. latifoliaCaffeic acid derivatives[3]
Ethyl caffeate[5]
3,4-di-O-caffeoylquinic acid methyl ester
3,5-di-O-caffeoylquinic acid methyl ester
Chlorogenic acid
Yerba MateIlex paraguariensis A. St.-HilHydroxycinnamic acid derivatives[18]
Flavonols
3-caffeoylquinic acid
5-caffeoylquinic acid
4-caffeoylquinic acid
3, 5-dicaffeoylquinic acid
Rutin
Yaupon hollyI. vomitoriaRutin[20,21]
Chlorogenic acid[21]
Neochlorogenic acid
Cryptochlorogenic acid
GuayusaI. guayusaChlorogenic acid[22,24]
Isochlorogenic acid[22]
Neochlorogenic acid

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Gan, R.-Y.; Zhang, D.; Wang, M.; Corke, H. Health Benefits of Bioactive Compounds from the Genus Ilex, a Source of Traditional Caffeinated Beverages. Nutrients 2018, 10, 1682. https://doi.org/10.3390/nu10111682

AMA Style

Gan R-Y, Zhang D, Wang M, Corke H. Health Benefits of Bioactive Compounds from the Genus Ilex, a Source of Traditional Caffeinated Beverages. Nutrients. 2018; 10(11):1682. https://doi.org/10.3390/nu10111682

Chicago/Turabian Style

Gan, Ren-You, Dan Zhang, Min Wang, and Harold Corke. 2018. "Health Benefits of Bioactive Compounds from the Genus Ilex, a Source of Traditional Caffeinated Beverages" Nutrients 10, no. 11: 1682. https://doi.org/10.3390/nu10111682

APA Style

Gan, R.-Y., Zhang, D., Wang, M., & Corke, H. (2018). Health Benefits of Bioactive Compounds from the Genus Ilex, a Source of Traditional Caffeinated Beverages. Nutrients, 10(11), 1682. https://doi.org/10.3390/nu10111682

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