INDIA GreenTea Easy Bioq2
INDIA GreenTea Easy Bioq2
E-ISSN: 2321-2187
P-ISSN: 2394-0514
www.florajournal.com The beneficial effects of green tea on human health: an
IJHM 2020; 8(5): 63-73
Received: 24-07-2020 updated review
Accepted: 29-08-2020
Mir Monir Hossain Mir Monir Hossain, Shahrin Mahmood and Tasmuna Tamrin Tanmy
1. Ph.D., Scholar, Department of
Chemistry, Cleveland State
University (CSU), Cleveland, Abstract
Ohio, USA Green tea is un-fermented product of Camellia species. The leaves of both Camellia sinensis and
2. Associate Professor, Camellia assamica, are used for the production of green tea, but C. assamica is mainly used for the
Department of Pharmacy, production of black tea. Green tea is widely produced from the leaves of C. sinensis, now a day’s which
University of Science & is one of the most popular beverages worldwide. Over the past 50 years or more, scientists have studied
Technology Chittagong this plant with respect to potential health benefits. Research has shown that the main components of
(USTC), Foy’s Lake, green tea that are associated with health benefits are the catechins. The four main catechins found in
Chittagong, Bangladesh green tea are: (-)-epicatechin (EC), (-)-epicatechin-3-gallate (ECG), (-)-epigallocatechin (EGC), and (-)-
epigallocatechin-3-gallate (EGCG). Of these four, EGCG is present in the largest quantity, and so has
Shahrin Mahmood
been used in most of the researches. Among the important health benefits of green tea are:
Department of Pharmacy,
anticarcinogenic, anti-inflammatory, antioxidant, and antimicrobial properties, and benefits in
University of Science &
Technology Chittagong (USTC), cardiovascular disease and oral health. Research has been carried out using various animal models and
Foy’s Lake, Chittagong, cells lines, and is now more and more being carried out in humans. This type of research will help us to
Bangladesh better understand the direct benefits of green tea. This review will focus primarily on researches
conducted on human subjects to investigate the health benefits of green tea.
Tasmuna Tamrin Tanmy
Department of Pharmacy, Keywords: Greentea, anticancer, anti-inflammatory, antimicrobial, antioxidant, cardiovascular disease,
University of Science & oral health, metal ions
Technology Chittagong (USTC),
Foy’s Lake, Chittagong,
1. Introduction
Bangladesh
Green tea, native to China, India and Bangladesh, has been consumed and hailed for its health
benefits for centuries globally. Tea is the most consumed beverage in the world behind water.
However, 78 percent of the tea consumed worldwide is black and only about 20 percent is
green. All types of tea, except herbal tea, are brewed from the dried leaves of the C.sinensis
bush. The level of oxidation of the leaves determines the type of tea. Green tea is made from
unoxidized leaves and is one of the less processed types of tea. It, therefore contains the
most antioxidants and beneficial polyphenols. Cultivation of tea plants is economically
important in many countries, and is known to be grown in as many as 40 countries. C. sinensis
grows best in certain tropical and subtropical regions [1]. There are four main types of tea
produced from this same plant, depending on how the tea leaves are processed. These teas are
white, green, Oolong, and black tea. White tea is produced from very young leaves and buds
that have not yet turned green, and the only processing is drying. Green tea is produced from
mature leaves with minimal processing (only drying). Oolong tea is produced from partially
fermented mature leaves, and black tea is produced from fully fermented mature leaves [1,2].
Green tea, which makes up around 20% of tea production worldwide, is consumed most often
in China, Korea, India, Bangladesh and Japan. Oolong tea is consumed most in China and
Taiwan. Black tea (around 78% of tea production) is mostly consumed in the United States
and the United Kingdom. Black tea contains up to three times the amount of caffeine as green
tea [3–5]. Like other drugs or nutrients within our system, the health beneficial effects of green
tea solely depend on bioavailability after its consumption. In recent years, the health benefits
[6]
Corresponding Author: of consuming green tea, including the prevention of cancer [7] and cardiovascular diseases [8],
Mir Monir Hossain the anti-inflammatory [9], antiarthritic [10], antibacterial [11], antiangiogenic [12],antioxidative [13],
1. Ph.D., Scholar, Department of antiviral [14], neuroprotective [15], andcholesterol-lowering effects [16] of green tea and isolated
Chemistry, Cleveland State green tea constituents are under investigation. However, adding green tea to the diet may cause
University (CSU), Cleveland, other serious health concerns.The risk of the tea catechins can affect iron absorption,
Ohio, USA
2. Associate Professor, particularly in group of people who have iron deficiency. Green tea ingestion over a long
Department of Pharmacy, period does not affect the apparent absorption of copper, whereas it decreases that of zinc and
University of Science & increases that of manganese. However, catechin intake does not affect the blood plasma
Technology Chittagong concentration of these ions. Green tea catechins have the potential to affect absorption and
(USTC), Foy’s Lake, metabolism of ions because flavonoids interact with a variety of metal ions.
Chittagong, Bangladesh
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International Journal of Herbal Medicine http://www.florajournal.com
1.1 Phytochemical Constituents polyphenol oxidase. To prevent loss of the polyphenols, green
The active components of green tea that are the most health- tea leaves are heated rapidly (most commonly by steaming or
promoting relevant medically are the polyphenols, with the pan frying) to inactivate polyphenol oxidase. Black tea leaves
flavonoids being the most important. The most pertinent are dried, then rolled and crushed, which promotes oxidation.
flavonoids are the catechins, which make up80%–90% of the Therefore, black tea has far fewer active catechins than green
flavonoids, and approximately 40% of the water-soluble tea. Green tea contains four main catechins: (-)-epicatechin
solids in green tea [17–19]. The amount of catechins in the tea (EC), (-)-epigallocatechin (EGC), (-)-epicatechin-3-gallate
can be affected by which leaves are harvested, how the leaves (ECG), and (-) epigallocatechin-3-gallate (EGCG). The most
are processed, and how the tea is prepared. In addition, where abundant of these in green tea is EGCG, which represents
the leaves are grown (geographically) and the growing around 59% of total catechins. The next most abundant is
conditions affect catechin amounts [20–23]. Polyphenols are EGC (around 19%), then ECG (around 14%), and EC (around
quickly oxidized after harvesting due to the enzyme 6%).
The chemical composition of green tea is made up of 15-20% fermentation and drying which areinvolved to make a finished
protein, 1-4% amino acids, 30% phenolic compounds, 7% product [27]. The color oftea leaves changes after all the steps
lipids, 7% carbohydrates, 26% fibers, 5% minerals and 2% from green tocopper brown and gives a floral smell. The
pigments on a dry weight basis[24] (See Fig 1). Amino acids leaves are heated immediately, mechanically wound,
like glutamic acid, tryptophan, glycine, serine, aspartic acid, compressed and then shade dried to preserve theirnatural
tyrosine, valine, leucine, threonine, arginine, and lysine and components and color.
carbohydrates (5-7% in dry weight basis) such as cellulose,
pectins, glucose, fructose, sucroseare partly included in green 2. Green tea processing
tea [25]. Other green tea-compounds with interest in human The vital steps of green tea processing are as below:
health such as fluorine, caffeine, trace elements such as Fresh leaves collection → sorting and cleaning → withering
chromium and manganese [26]. It contains trace elements in (often) → panfrying or steaming → drying.
lipid form (linoleic acid, alpha-linolenic acid), sterols The discrete features of green tea processing isthat, the leaves
(stigmasterol), vitamins (B, C, E), xanthine bases (caffeine, are never subjected to fermentationprocess. Instead, the leaves
theophylline), pigments (chlorophyll, carotenoids), volatile are steamed (95-100ºC) for 30-45 seconds immediately after
compounds (aldehyde, alcohol, esters, lactones, harvesting, toinactivate the enzymes and protect degradation
hydrocarbons). ofvitamins. For this reason, the green tea contains
morevitamin contents in comparison to black tea. Thefresh
1.2 Processing of tea leaves leaves contain 78-80% polyphenols, whichdecreases to about
The green and black teas are the products of thesame plant, 10% during rolling process. Thedrying process is crucial to
but the basic difference lies in their processing. Black tea is preserve the aroma andstorage capacity.
the fermented product andundergoes fermentation process
before drying, Whereas, black tea is made by oxidation 3. Black tea processing
process. Afterplucking, leaves are subjected to the process of The major steps of black tea processing can be shown as
withering (removal of moisture by air flow), preconditioning, follows:
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Fresh leaves collection → Withering → Rolling by tea roller beverage or a supplement containing mixed catechins may be
or CTC (crushing, tearing, curling) → Fermenting → Drying more effective than using single catechin (e.g., EGCG)
After following these steps, the fermentation step plays a supplements [38].The potential molecular mechanisms and
crucial role in maintaining quality of blacktea. The oxidation targets that might explain how green tea catechins possess
process predominantly oxidizes the catechins present in tea anticarcinogenic properties have been widely studied (using
leaves. The moisture content in the tea leaves is evaporated various cell cultures, etc.), especially in breast cancers. These
and leaves become flaccid. The black tea is made by a CTC include interaction with specific proteins, anti-angiogenesis
machine. In many countries such as India, Kenya and Sri mechanisms, targets for inhibition of enzyme activities and
Lanka, CTC process of tea making are being followed. But, cell signaling pathways, and induction of cell cycle arrest and
China follows its traditional “orthodox rollers” process. For apoptosis [39]. The mushrooming area of nanotechnology has
the fermentation of black tea, warm temperature (25-35ºC) led to the development of potential chemotherapy involving
and high humidity (~95%) are required. The fermentation nanoparticles (NPs). Various particles (e.g., gold) can be used
process depends on the variety of plant and age of tea leaves. to deliver compounds to specific areas of the body. Research
It takes half hour to three hours to complete the fermentation using EGCG and nanoparticles has already begun using a
process. Generally, CTC machine takes less time (30 to 60 number of delivery approaches. These include: coating an NP,
minutes), while orthodox roller takes 2-3 hours. such as gold, with EGCG; use of encapsulated (in liposomes
or polymeric NPs) EGCG in NPs along with anti-cancer
4. Anticancer properties drugs, outer ligands that will bind to specific targets, or outer
Now days, cancer is a major cause of morbidity and mortality polymers that will enhance the intestinal absorption of EGCG
[32]
worldwide. Billions of dollars have been poured into cancer .
research over the past 60 years, and still we do not seem to be
any closer conclusion to actually curing it. In addition, quite 5. Cardiovascular disease (CVD) health benefits:
often the chemotherapies do as much, if not more damage to At present, Cardiovascular disease (CVD) is a leading cause
the patient as the disease. Because cancer appears in so many of death and a complex disorder involving multiple factors.
different forms inmultiple parts of the body, it has been The factors those involve in CVD are: inflammation,
difficult to determine the mechanisms that lead to the disease. oxidative stress, platelet aggregation, obesity and lipid
Even with what we now know about cancer risk factors, there metabolism. Some of these factors are also involved in other
are still many people who seemingly have none of the risk disease processes but will be discussed in this paper under
factors, and yet succumb to a rapidly aggressive form. CVD. There have been a number of studies over the years
Encouraging people to think about how a healthy lifestyle can assessing green tea consumption in respect to CVD risk [40].
prevent disease is certainly a step in the right direction, and it Very recently, two studies from Japan that included nearly
would be most helpful to identify substances that could be 50,000 people found a decreased mortality rate due to CVD
useful in prevention and treatment. Green tea is an based on consumption of various numbers of cups per day.
exceptional cancer-preventive prescription with two features One study showed a 28% decrease in CVD death between
as refreshment and medication. Herbal remedies, including those who consumed ≤ 3 cups and those who consumed more
green tea, are the same old thing, yet by presenting the idea of than ≥ 10 cups. The other study showed a 14% decrease in
malignant growth counteractive action that green tea spares CVD mortality between those who consumed <1 cup and
individuals' lives. The supremecomponent of green tea that those who consumed ≥ 5 cups [41,42]. In Japan, Other studies
has been studied in cancer research is EGCG. There using a green tea extract found that, after 12 weeks, the
areseveral cancer related mechanisms attributed to EGCG. subjects had reductions in body fat (10%), blood pressure
These include: inhibition of angiogenesis, DNA (6.5%), and low-density lipoprotein (LDL) levels (2.6%),
hypermethylation, NF-kB, telomerase activity, and tumor cell suggesting reduced risk of CVD. After two months, diabetic
proliferation and metastasis; inductionof tumor suppressor patients also had reduced fasting blood glucose levels (from
genes; and promotion of tumor cell apoptosis [28–32]. Inhibition 135 to 128.8 mg/dL), and hemoglobin A1c (HBA1c) levels
of angiogenesisis suggested to occur through a decrease in (from 6.2% to 6.0%) [43,44]. A large meta-analysis of 17
RNA and peptide levels of vascular endothelial growthfactor studies from over 30 years, including data from Europe, the
(VEGF), and by disrupting the dimerization of VEGF with the UK, and the U.S., found that increasing consumption of green
vascular endothelial growth factorreceptor 2 (VEFR2) [33]. tea by three cups per day decreased the risk of myocardial
Another suggested way in which green tea catechins may infarction (MI) death by 11% [45]. Another study showed a
generally inhibitcarcinogenesis is through increasing levels of decreased risk of mortality in patients who had an acute MI
glutathione S-transferase pi (GST-pi), which and a history of regular green tea consumption for at least a
catalyzesdetoxification reactions that inhibit carcinogen- year prior to the MI. Participants who did not drink green tea
induced DNA damage [34].Analysis of studies performed by had a 14% rate of death due to the MI; participants who drank
using human oral consumption of green tea to assess cancer up to 14 cups per week had an 11% rate of MI death; and
risk showed that case-control studies gave the most consistent participants who drank more than 14 cups per week had a
results and were positive for reduced cancer risk in breast, 10% rate of MI death [46]. An interesting study in patients with
cardiac, colorectal, esophageal, gastric, lung, ovarian, CVD showed that consumption of EGCG resulted in a rapid
pancreatic, and prostate cancers [35,36]. A recent large study improvement of vascular endothelial function. Participants
showed a relationship between breast cancer risk and tea who ingested an initial dose of 300 mg of EGCG had an
consumption, with the risk being highest in the groups that improved brachial artery flow-mediated dilation from 7.1% to
did not consume tea and lowest in the groups that consumed 8.6% after 2 h [47]. Another recent study found that increased
the most cups per day. Number of cups were assessed in five intake of dietary flavonoids was associated with a decreased
categories (0.1–1.0 cups, 1.1–2.0 cups, 2.1–3.0 cups, 3.1–5.0 risk of CVD. The participants were divided into three groups
cups, >5.0 cups) [37]. Analysis of the types of green tea based on average daily consumption of flavonoids. The first
beverage or extracts used in studies suggests that green tea tertile consumed 89 mg/day, the second tertile consumed 251
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International Journal of Herbal Medicine http://www.florajournal.com
mg/day, and the third tertile consumed 532 mg/day. The catechins have been found to have antioxidant activity
number of deaths due to CVD in the first tertile was 8.6%; in through: inhibiting redox sensitive transcription factors and
the second tertile, 6.4%; and in the third tertile, 5.0% [48]. pro-oxidant enzymes, scavenging ROS, and inducing anti-
oxidant enzymes.
5.1. Inflammation Studies to determine the antioxidant capabilities of green tea
Rather than the CVD, inflammation is also involved in may measure a variety of substances. Tests may measure the
arthritis, aging, cancer, etc. Many of the anti-inflammatory presence of known ROS or their metabolites, such as
effects when using green tea have been studied in rheumatoid hydroxyl radical, peroxides, superoxide, and singlet oxygen.
arthritis (RA) and osteoarthritis (OA), and are pertinent to Other measurements may be for known antioxidant
CVD as well. Some general anti-inflammatory mechanisms of substances such as superoxide dismutase (SOD) and
green tea components are: increased production of the anti- glutathione peroxidase, or substances that indicate
inflammatory cytokine, IL-10; regulation of IL-6 synthesis inflammation such as high-sensitivity C-reactive protein (hs-
and signaling; decreased production of destructive matrix CRP) and TNF-α. Another type of testing assesses total
metalloproteinases via TNF-α induced phosphorylation of antioxidant capacity (TAC), also known as total antioxidant
mitogen-activated protein kinases (MAPKs); and decreased status (TAS), which measures the amount of oxidants that are
expression of the chemokine receptor CCR2 and decreased neutralized in the body (e.g., moles of oxidant neutralized by
levels of the proinflammatory cytokines IL-1β and TNF-α [49– 1 L of plasma), with a lower number translating into a higher
52]
.The specific studies on inflammation can be roughly risk of disease [49].The results from recent studies have shown
categorized into: inhibition of neutrophil-endothelium that green tea catechins can affect levels of ROS [61–64],
interaction, modulation of neutrophil functions and death, and increase levels of antioxidants [65–68], decrease levels of
regulation of inflammation factors. Neutrophil migration and inflammatory substances [69,70], and increase TAC (TAS)
[66,68,69]
function are an integral part of the inflammatory response, so . An excellent summary of earlier studies that
controlling neutrophils is vital in decreasing inflammation. measured ROS and TAC can be found in a chapter by Serafini
Studies have shown that green tea catechins cause a reduction et al. 2011 [49].
in the number of leukocyte-endothelial cell adhesion The antioxidant activity of green tea polyphenols is
molecules (CAMs), such as ICAM-1, VCAM-1, and E- predominantly due to the combination of aromatic rings and
selection, expressed on the endothelial cell surface. This hydroxyl groups, which synthesize their chemical structure
restricts the ability of the neutrophils to migrate to sites of and consequently bind and neutralize lipid-free radicals by
infection [53,54]. Other studies have shown that factors known these hydroxyl groups. Numerous researches have been
to regulate neutrophil function, such as IL-1 β, IL-2, TNF-α, exhibited in different aspects on antioxidant activity of green
and granulocyte-macrophage colony-stimulating factor (GM- tea polyphenols which are exceptional electron donors and are
CSF), are suppressed by consumption of green tea or EGCG, effective scavengers of physiologically reactive oxygen
resulting in inhibition of inflammation [55–57]. Studies on the species (ROS) in vitro, including superoxide anions [71].
inhibition of pro-inflammatory factors have shown that green Consequently, green tea is the most effective against beta-
tea catechins downregulate many inflammatory chemokines, carotene oxidation as far as the antioxidant property is
cytokines, and inflammatory markers such as: IL-1α, IL-1β, concerned and can serve as a natural source of free radical
IL-6, IL-8, Interferon gamma (INF-ϒ), and C-reactive protein scavengers and cancer prevention agent [72]. The most potent
(CRP) [56,58–60]. antioxidant polyphenol of green tea is EGC. Again, radical
scavenging is high in the gallocatechin including EGCG and
5.2. Oxidative Stress EGC. Many studies have been reported on green tea that has
Oxidative stress in the body is closely connected to much higher antioxidant activities against free radicals which
inflammation and CVD, and is the result of the damaging are not found in vegetables. It is measured mainly by the
effects of reactive oxygen species (ROS). These ROS are Oxygen Radical Absorbance Capacity (ORAC) assay, DPPH
capable of causing chronic inflammation through induction of (2, 2-diphenyl-1-picrylhydrazyl) radical scavenging assays
inflammatory cytokines and chemokines, and pro- and Trolox equivalent antioxidant capacity (TEAC) assay
inflammatory transcription factors. In general, green tea (See Fig 2)[13, 73-74,].
5.3. Platelet Aggregation reports demonstrated that green tea catechin, EGCG is the
Platelet activation and subsequent aggregation play an most active compound against HIV infectious diseases [107].
important role in CVD. When the vascular endothelium is Furthermore, the evaluation has also been done with herpes
damaged, platelets usually respond rapidly and aggregate to simplex virus (HSV) and bovine coronavirus (BCV) to realize
form plugs at the damage site, and may also form clots that the resistance power of antiviral activity and therapeutic
could lead to vessel occlusion [75]. Many of the studies on efficiency of catechin polyphenols [108].
platelet aggregation have been carried out using various
animal platelets. In addition to showing that green tea 7. Oral Health Benefits
catechins were involved in inhibition of platelet aggregation, Recently, research has launched to focus on the effects of
studies suggested that, catechins may affect several cellular green tea on oral health. Two of the general ways in which
targets that are related to platelet activation, including: green tea consumption helps oral health are due to its anti-
through the arachadonic acid pathway, inhibition of a inflammatory properties, and antimicrobial activity against
cytoplasmic increase in calcium, decreased thromboxane A 2 mouth flora such as Streptococcus mutans [109, 110]. The
(TXA2) production, and inhibition of cyclooxygenase-1 antimicrobial activity may also be responsible for the
(COX-1)) [76–79]. A study using human platelets concluded that improvement observed as to bad breath [111]. The two major
EGCG was able to inhibit platelet activation by adenosine types of effects on oral health are a decrease in periodontist
diphosphate (ADP) stimulation, and suppressed the p38 and dental caries.
MAPK phosphorylation of heat shock protein 27 (HSP27),
which would inhibit the release of pro-thrombotic contents 7.1. Periodontitis
from platelets [80]. Green tea consumption has been found to result in decreased
tooth loss,and prevent the development and progression of
5.4. Lipid Metabolism periodontitis. Green tea consumption also has positive effects
Increased blood lipid levels have long been suspected as an on periodontal health when assessed as to probing depth,
increased risk for CVD, especially LDLs [81]. One mechanism attachment loss, gingival bleeding, and dentin erosion. In
that is linked with atherosclerosis is the presence of oxidated addition to the antimicrobial effects on the main bacteria
LDL [82]. There have been many studies performed using involved in gingivitis, Porphyromonasgingivalis, EGCG has
human subjects to determine the effect of green tea catechins been shown to inhibit the ability of the bacteria to bind to oral
on lipids. The studies have reported that consumption of green epithelial cells via fimbriae, and has also been shown to
tea catechins lowers total cholesterol and LDL levels and also inactivate bacterial collagenases. EGCG also inhibits
reduces blood pressure [83–90]. In addition, a recent study found production of matrix metalloproteins and IL-8, which are
that green tea catechins are incorporated into LDL particles, responsible for initiating tissue destruction [109,110,112,113].
and are then able to reduce the oxidation of LDL. Catechins
prevent LDL oxidation via radical-trapping abilities and act as 7.2. Dental Caries
hydrogen donors to α-tocopherol radicals [91]. Prevention of dental caries is attributed to the ability of
EGCG to bind and inhibit salivary and bacterial amylases, in
6. Antimicrobial action particular, α-amylase. EGCG also prevents generation of acid
Resistance to antimicrobial agents has been becoming from carbohydrates through inhibiting the transcription and
harmful to the environment and accelerating the global function of LDH. One of the main things that encourages
problem [92]. Nowadays many antimicrobial drugs cannot tooth decay is that the major oral bacteria (e.g., Streptococcus
destroy their pathogenic microorganisms as they are mutans) form a biofilm on the surface of teeth. EGCG inhibits
becoming resistant. Therefore, researchers are finding some the adherence of the bacteria to teeth, decreases biofilm
new drugs from mangrove species to control the pathogens formation, and inhibits the ability of the bacteria to produce
due to the presence of antimicrobial compounds [93, 94]. The an acid environment. EGCG also inhibits the hydrogen
antimicrobial activity of tea was first established almost 100 binding and hydrophobic interactions of bacterial
years ago[95,96]. Green tea exhibits antimicrobial properties, collagenases. Consumption of green tea has also been
which are ascribed predominantly to its polyphenols [97]. The associated with an increase in oral peroxidase activity [113–115].
degree of animation depends on the bacterial species and the
polyphenol structure [98, 99]. Good evidence suggests that the 8. Effect on diabetes
catechin components of green tea are responsible for the A study by Waltner-Law et al. [116] provided compelling in
observed antibacterial activity owing to the presence of EGC, vitro evidence that EGCG decreases glucose production of
EGCG, and ECG constituents [100, 101]. Gram-negative bacteria H4IIE rat hepatoma cells. The investigators showed that
seem to be more resistant to polyphenols than Gram-positive EGCG mimics insulin, increases tyrosine phosphorylation of
bacteria, due to differences in the exterior membrane [102]. The the insulin receptor and the insulin receptor substrate, and
main components responsible for the antimicrobial activity reduces gene expression of the gluconeogenic enzyme
are EGCG and EGC. EGCG at 10–100 μm has shown to phosphoenolpyruvate carboxykinase. Recently, green tea and
reduce E. Coli growth by approximately 50% [103]. The green tea extracts were demonstrated to modify glucose
mechanism of antiviral action of polyphenolic compounds is metabolism beneficially in experimental models of type II
based on various capacities to go about as antioxidant agents, diabetes mellitus [117]. In addition, EGCG ameliorates
to inhibit proteinaceous enzymes, to disrupt cell membranes, cytokine induced beta cell damage in vitro [118] and prevents
to avoid viral binding and penetration into cells, and to trigger the decrease of islet mass induced by treatment with multiple
the host cell. EGCG hinders infections by direct authoritative low doses of streptozotocin in vivo [119].
to biological molecules and persuades agglutination of the flu
infection preventing their adsorption to target [104]. The 9. Effect on obesity
antiviral mechanism of EGCG has been analyzed against The effects of green tea on obesity have received increasing
endemic HBV (Hepatitis B virus) infection [105, 106]. Many attention. Tea catechins, especially EGCG, appear to have
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anti-obesity [120]. African black tea extract has been shown to against carcinogens involving only modulation of this
suppress the elevation of blood glucose during food intake metabolic pathway.
and reduce the body weight in KK-A(y)/TaJcl diabetic mice
[121]
. Although few epidemiological and clinical studies have 12. Adverse effects of green tea
shown the health benefits of EGCG on obesity and diabetes, Although green tea has several beneficial effects on
the mechanisms of its actions are emerging based on various humanhealth, the effects of green tea and its constituents
laboratory data. These mechanisms may be related to certain maybe beneficial up to a certain dose, yet higher doses
pathways, such as through the modulations of energy balance, maycause some unknown adverse effects. Harmful effects of
endocrine systems, food intake, lipid and carbohydrate tea overconsumption (black or green) are due to three main
metabolism, and redox status [122].It has been reported that the factors: (1) its caffeine content, (2) the presence of aluminum,
body weights of rats and their plasma triglyceride, cholesterol, and (3) the effects of tea polyphenols on iron bioavailability.
and low-density lipoprotein cholesterol were significantly Green tea should not be taken by patients suffering from heart
reduced by feedings of Oolong, black, and green tea leaves to conditions or major cardiovascular problems. Pregnant and
the animals. When fed to mice, EGCG purified from green tea breastfeeding women should drink no more than one or two
decreased diet-induced obesity in mice by decreasing energy cups per day, because caffeine can cause an increase in heart
absorption and increasing fat oxidation [123]. The increased and rhythm. It is also important to control the concomitant
prolonged sympathetic stimulation of thermogenesis by the consumption of green tea and some drugs, due to caffeine’s
interaction between polyphenols and caffeine could be of diuretic effects [134]. Some studies revealed the capacity of tea
value in assisting the management of obesity [124]. Recent data plants to accumulate high levels of aluminum. This aspect is
from human studies indicate that the consumption of green tea important for patients with renal failure because aluminum
and green tea extracts may help reduce body weight, mainly can be accumulated by the body, resulting in neurological
body fat, by increasing postprandial thermogenesis and fat diseases; it is therefore necessary to control the intake of food
oxidation. These findings suggest that, EGCG alone has the with high amounts of this metal [135]. Likewise, green tea
potential to increase fat oxidation in human and may thereby catechins may have an affinity for iron, and green tea
contribute to the anti-obesity effects of green tea. However, infusions can cause a significant decrease of the iron
more studies with a greater sample size and a broader range of bioavailability from the diet [136]. Moreover, theeffects of
age and body mass index (BMI) are needed to define the green tea catechins may not be similar in all individuals.
optimal dose [125]. EGCG of green tea extract is cytotoxic, and higher
consumption of green tea can exert acute cytotoxicity in liver
10. Effects on absorption of metal ions cells, a major metabolic organ in the body [137]. Another study
Green tea’s catechins can affect iron absorption, particularly found that higher intake of green tea might cause oxidative
in groups at risk of iron deficiency [126, 127] but their effects on DNA damage of hamster pancreas and liver [138]. Yun et al.
[139]
other ions are poorly understood. Green tea ingestion over a clarified that EGCG acts as a pro-oxidant, rather than an
long period does not affect the apparent absorption of copper, antioxidant, in pancreatic b cells in vivo. Therefore, high
whereas it decreases that of zinc and increases that of intake of green tea may be detrimental for diabetic animals to
manganese [128]. However, catechin intake does not affect the control hyperglycemia. At a high dose (5% of diet for 13
plasma concentration of these ions [129]. Green tea catechins weeks), green tea extract induced a thyroid enlargement
have the potential to affect absorption and metabolism of ions (goiter) in normal rats [140]. This high-level treatment modified
because flavonoids interact with a variety of metal ions [130]. the plasma concentrations of the thyroid hormones. However,
drinking even a very high dietary amount of green tea would
11. Effects on drug-metabolizing enzymes be unlikely to cause these adverse effects in humans.
Long-term ingestion of green tea increases UDP-glucuronosyl
transferase activity in rats [131] and after being absorbed, 13. Conclusion
catechins are metabolized by drug metabolizing enzymes in The beneficial effects of green tea are being increasingly
various organs [132]. Thus, the increased glucuronidation recognize day by day, so it could be recommended that
through UDP-glucuronosyl transferase induction is postulated consumption of tea on regular basis. Green tea contains
to contribute to the anticarcinogenic effect of green tea by polyphenols, which include flavanols, flavandiols, flavonoids
facilitating the metabolism of chemical carcinogens into and phenolic acids; these compounds may account for up to
inactive products that are readily excreted. The interaction 30% of the dry weight. It is the reach source of phytonutrients
between 2-amino-3-methylimidazol quinoline (IQ) and green like flavonoids, phenolic acids, polyphenols, and catechin
tea catechin metabolism was examined [133]. IQ is a pre- tannins. Green tea catechins have proved to be very versatile
carcinogen that was originally detected in an extract of fried in providing health benefits. This means that there are
meat. The major route of IQ biotransformation in rats is potential health benefits for everyone in the consumption of
cytochrome P-450 in the first step, followed by conjugation to green tea. Even moderate amounts of consumption (drinking
a sulfate and a glucuronide conjugate. Green tea modifies IQ 1–2 cups of tea per day) may have benefits. It is a very good
metabolism in rats, increasing the formation of IQ thing that it is the second most popular beverage worldwide,
glucuronides, which are then excreted in the urine. Moreover, as the differences in health in a world without green tea might
protection against cancers induced by polycyclic aromatic be significant. Green tea also has several hydrophilic
hydrocarbons by green tea catechins may be due to the antioxidants properties as Trolox and free radical scavengers.
inhibition of their cytochrome P-450 metabolism, but the Unlike coffee, green tea contains an amino acid L-theanine,
effect of green tea on cytochrome P-450 enzymes depends on that prevents caffeine rush and gives you the energy to sustain
the particular form. The long-term consumption of green tea throughout several hours instead. Fortunately, there is a wide
increases cytochrome P-450 1A1 and 1A2 activities, but not variety of research being performed using green tea catechins,
2B1 and 2E1 activities, in normal rats. However, it is difficult and we are starting to see many studies performed using
to draw conclusions about a beneficial effect of green tea human subjects, as it is extremely important that we are able
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International Journal of Herbal Medicine http://www.florajournal.com
to show the direct benefits to humans. Laboratory studies cells. J Nutr. 2002; 132:2307-2311.
already showed the health effects of green tea. As the human 13. Hossain MM, Mahmood S. In vitro studies on
clinical evidence is still limited, future research needs to antibacterial, thrombolytic and antioxidant activities of
define the actual magnitude of health benefits, establishes the green tea or Camellia sinensis. Am. J. Phytomed. Clinic.
safe range of tea consumption associated with these benefits, Therap.2014; 2:1200-1211.
and elucidates the mechanisms of action. Development of 14. Weber JM, Ruzindana-Umunyana A, Imbeault L, Sircar
more specific and sensitive methods with more representative S. Inhibition of adenovirus infection and adenain by
models along with the development of good predictive green tea catechins. Antiviral Res. 2003; 58:167-173.
biomarkers will give a better understanding of how green tea 15. Weinreb O, Mandel S, Amit T, Youdim MBH.
interacts with endogenous systems and other exogenous Neurological mechanisms of green tea polyphenols in
factors. Definitive conclusions concerning the protective Alzheimer’s and Parkinson’s diseases. J Nutr Biochem.
effect of green tea have to come from well-designed 2004; 15:506-516.
observational epidemiological studies and intervention trials. 16. Raederstorff DG, Schlachter MF, Elste V, Weber P.
The expansive repertoire of green tea activity in health is Effect of EGCG on lipid absorption and plasma lipid
important, especially to those people who live in areas where levels in rats. J Nutr Biochem. 2003; 14:326-332.
medical assistance is not generally available or affordable. 17. Wang Y, Ho CT. Polyphenolic chemistry of tea and
The development of biomarkers for green tea consumption, as coffee: A century of progress. J. Agric. Food Chem.
well as molecular markers for its biological effects, will 2009; 57:8109-8114.
definitely facilitate future research in this area. 18. Roowi S, Stalmach A, Mullen W, Lean ME, Edwards
CA, Crozier A. Green tea flavan-3-ols: Colonic
14. Conflicts of Interest: The author declares no conflicts of degradation and urinary excretion of catabolites by
interest. humans. J. Agric. Food Chem. 2010; 58:1296-1304.
19. Babu PV, Liu D. Green tea catechins and cardiovascular
15. References health: An update. Curr. Med. Chem. 2008; 15:1840-
1. Gupta DA, Bhaskar DJ, Gupta RK, Karim B, Jain A, 1850.
Dalai DR. Green tea: A review on its natural antioxidant 20. Fernandez PL, Pablos F, Martin MJ, Gonzalez AG. Study
therapy and cariostatic benefits. Biol. Sci. Pharm. Res. of catechin and xanthine tea profiles as geographical
2014; 2:8-12. tracers. J. Agric. Food Chem. 2002; 59:1833-1839.
2. Jigisha A, Nishant R, Navin K, Pankaj G. Green tea: A 21. Lin YS, Tsai YJ, Tsay JS, Lin JK. Factors affecting the
magical herb with miraculous outcomes. Int. Res. J. levels of tea polyphenols and caffeine in tea leaves. J.
Pharm. 2012; 3:139-148. Agric. Food Chem. 2003; 51:1864-1873.
3. Cabrera C, Artacho R, Gimenez R. Beneficial effects of 22. Liu M, Tian HI, Wu JH, Cao RR, Wang RX, Qi XH et al.
green tea-A review. J. Am. Coll. Nutr. 2006; 25:79-99. Relationship between gene expression and the
4. Botten D, Fugalio G, Fraternali F, Molteni C. Structural accumulation of catechin during spring and autumn in tea
properties of green tea catechins. J. Phys. Chem. B. 2015; plants (Camellia sinensis L.). Hortic. Res. 2015; 2:15011.
119:12860-12867. 23. Lantano C, Rinaldi M, Cavazza A, Barbanti D, Corradini
5. Hayat K, Iqbal H, Malik U, Bilal U, Mushtaq S. Tea and C. Effects of alternative steeping methods on
its consumption: Benefits and risks. Crit. Rev. Food Sci. composition, antioxidant property and colour of green,
Nutr. 2015; 55:939-954. black and oolong tea infusions. J. Food Sci. Technol.
6. McKay DL, Blumberg JB, The role of tea in human 2015; 52:8276-8283.
health: An update. J Am Coll Nutr. 2002; 21:1-13. 24. Chacko SM, Thambi PT, Kuttan R, Nishigaki I.
7. Kavanagh KT, Hafer LJ, Kim DW, Mann KK, Sherr DH, Beneficial effects of green tea: a literature review.
Rogers AE et al. Green tea extracts decrease carcinogen- Chinese Medicine. 2010; 5(1):13.
induced mammary tumor burden in rats and rate of breast 25. Senanayake SN. Green tea extract: Chemistry,
cancer cell proliferation in culture. J Cell Biochem 2001; antioxidant properties and food applications–A review.
82:387-398. Journal of Functional Foods. 2013; 5(4):1529-1541.
8. Sueoka N, Suganuma M, Sueoka E, Okabe S, Matsuyama 26. Kristanti RA, Punbusayakul N. Antioxidant and
S, Imai K et al. A new function of green tea: prevention antimicrobial activity of commercial green tea in Chiang
of life style related diseases. Ann NY Acad Sci. 2001; Rai. In Asia Pacific Symposium on Assuring Quality and
928:274-280. Safety of Agri-Foods. 2008; 837:53-58.
9. Dona M, Dell’Aica I, Calabrese F, Benelli R, Morini M, 27. Robertson A. The chemistry and biochemistry of black
Albini A, Garbisa S. Neutrophil restraint by green tea: tea production-the non-volatiles. In Tea. Springer,
inhibition of inflammation, associated angiogenesis, and Dordrecht. 1992, 555-601
pulmonary fibrosis. J Immunol. 2003; 170:4335-4341. 28. Shirakami Y, Shimizu M, Moriwaki H. Cancer
10. Haqqi TM, Anthony DD, Gupta S, Ahmad N, Lee MS, chemoprevention with green tea catechins: From bench to
Kumar GK et al. Prevention of collagen-induced arthritis bed. Curr. Drug Targets. 2012; 13:1842-1857.
in mice by a polyphenolic fraction from green tea. Proc 29. Henning SM, Wang P, Carpenter CL, Heber D.
Natl Acad Sci USA. 1999; 96:4524-4529. Epigenetic effects of green tea polyphenols in cancer.
11. Hossain MM, Khanom RA, Yasmeen, Mahmood S, Epigenomics 2013; 5:729-741.
Tanmy TT. In vitro studies on antibacterial and 30. Subramani C, Natesh RK. Molecular mechanisms and
thrombolytic activities of black tea or Camellia sinensis. biological implications of green tea polyphenol, (-)-
Int. J. Inv. Pharm. Sci. 2013; 1(4):292-299. epigallocatechin-3-gallate. Int. J. Pharm. Biosci. Technol.
12. Sartippour MR, Shao ZM, Heber D, Beatty P, Zhang L, 2013; 1:54-63.
Liu C et al. Green tea inhibits vascular endothelial 31. Butt MS, Ahmad RS, Sultan MT, Qayyum MM, Naz A.
growth factor (VEGF) induction in human breast cancer Green tea and anticancer perspectives: Updates from last
~ 69 ~
International Journal of Herbal Medicine http://www.florajournal.com
decade. Crit. Rev. Food Sci. Nutr. 2015; 55:792-805. Boca Raton, FL, USA, 2011, 239-262.
32. Granja A, Pinheiro M, Reis S. Epigallocatechin gallate 50. Ahmed S, Marotte H, Kwan K, Ruth JH, Campbell PL,
nanodelivery systems for cancer therapy. Nutrients. 2016; Rabquer BJ et al. Epigallocaetchin-3-gallate inhibits IL-6
8:E307. synthesis and suppresses transsignaling by enhancing
33. Yang CS, Wang H, Li GX, Yang Z, Guan F, Jin H. soluble gp130 production. Proc. Natl. Acad. Sci. USA
Cancer prevention by tea: Evidence from 2008; 105:14692-14697.
laboratorystudies. Pharmacol. Res. 2011; 64:113-122. 51. Yun HJ, Yoo WH, Han MK, Lee YR, Kim JS, Lee SI.
34. Yang CS. Antioxidant and anti-carcinogenic activities of Epigallocatechin-3-gallate suppresses TNF-a-induced
tea polyphenols. Arch. Toxicol. 2009; 83:11-21. production of MMP-1 and -3 in rheumatoid arthritis
35. Ju J, Lu G, Lambert JD, Yang CS. Inhibition of synovial fibroblasts. Rheumatol. Int. 2008; 29:23-29.
carcinogenesis by tea constituents. Semin. Cancer 52. Leong DJ, Choudhury M, Hanstein R, Hirsh DM, Kim
Biol.2007; 17:395-402. SJ, Majeska RJ, Schaffler MB, Hardin JA. et al. Green
36. Boehm K, Borelli F, Ernst E, Habacher G, Hung SK, tea polyphenol treatment is chondroprotective, anti-
Milazzo S, Hornebar M. Green tea (Camellia sinensis) inflammatory and palliative in a mouse posttraumatic
for the prevention of cancer. Cochrane Database Syst. osteoarthritis model. Arthritis Res. Ther. 2014; 16:508.
Rev. 2009, 3. 53. Naito Y, Yoshikawa T. Green tea and heart health. J.
37. Bhoo-Pathy N, Peeters PH, Van Gils C, Beulens JW, Van Cardiovasc. Pharmacol. 2009; 54:385-390.
der Graaf Y, Bueno-de-Mesquita B et al. Coffee and tea 54. Liu D, Perkins JT, Hennig B. EGCG prevents PCB-126-
intake and risk of breast. Breast Cancer Res. Treat. 2010; induced endothelial cell inflammation via epigenetic
121:461-467. modifications of NF-B target genes in human endothelial
38. Bode AM, Dong Z. Epigallocatechin 3-gallate and green cells. J. Nutr. Biochem. 2016; 28:164-170.
tea catechins: United they work, divided they fall. Cancer 55. Donà M, Dell’Aica I, Calabrese F, Benelli R, Morini M,
Prev. Res. (Phila.) 2009; 2:514-517. Albini A et al. Neutrophil restraint by green tea:
39. Li MJ, Yin YC, Wang J, Jiang YF. Green tea compounds Inhibition of inflammation, associated angiogenesis, and
in breast cancer prevention and treatment. World J. Clin. pulmonary fibrosis. J. Immunol. 2003; 170:4335-4341.
Oncol. 2014; 5:520-528. 56. Akhtar N, Haqqi TM. Epigallocatechin-3-gallate
40. Jochmann N, Baumann G, Stangl V. Green tea and suppresses the global interleukin-1beta-induced
cardiovascular disease: From molecular targets towards inflammatory response in human chondrocytes. Arthritis
human health. Curr. Opin. Clin. Nutr. Metab. Care. 2008; Res. Ther. 2011; 13:r93.
11:758-765. 57. Behfarnia P, Aslani A, Jamshidian F, Noohi S. The
41. Nakachi K, Matsuyama S, Miyake S, Suganuma M, Imai efficacy of green tea chewing gum on gingival
K. Preventive effects of drinking green tea on cancer and inflammation. J. Dent. Shiraz Univ. Med. Sci. 2016;
cardiovascular disease: Epidemiological evidence for 17:149-154.
multiple targeting prevention. Biofactors. 2000; 13:49- 58. Kim IB, Kim DY, Lee SJ, Sun MJ, Lee MS, Li H et al.
54. Inhibition of IL-8 production by green tea polyphenols in
42. Kuriyama S, Shimazu T, Ohmori K, Kikuchi N, Nakaya human nasal fibroblasts and A549 epithelial cells. Biol.
N, Nishino Y et al. Green tea consumption and mortality Pharm Bull. 2006; 29:1120-1125.
due to cardiovascular disease, cancer, and all causes in 59. Tang Y, Matsuoka I, Ono T, Inoue K, Kimura J.
Japan: The Ohsaki study. JAMA 2006; 296:1255-1265. Selective up-regulation of P2X4-receptor gene expression
43. Nagao T, Hase T, Tokimitsu I. A green tea extract high in by interferon- in vascular endothelial cells. J. Pharmacol.
catechins reduces body fat and cardiovascular risks in Sci. 2008; 107:419-427.
humans. Obesity (Silver Spring) 2007; 15:1473-1483. 60. Liu X, Zhang DY, ZhangW, Zhao X, Yuan C, Ye F. The
44. Fukino Y, Shimbo M, Aoki N, Okubo T, Iso H. effect of green tea extract and EGCG on the signaling
Randomized controlled trial for an effect of green tea network in squamous cell carcinoma. Nutr. Cancer. 2011;
consumption on insulin resistance and inflammation 63:466-475.
markers. J. Nutr. Sci. Vitaminol. (Tokyo) 2005; 51:335- 61. Baba Y, Sonoda JI, Hayashi S, Tosuji N, Sonoda S,
342. Makisumi K et al. Reduction of oxidative stress in liver
45. Peters U, Poole C, Arab L. Does tea affect cardiovascular cancer patients by oral green tea polyphenol tablets
disease? A meta-analysis. Am. J. Epidemiol. 2001; 154: during hepatic arterial infusion chemotherapy. Exp. Ther.
495-503. Med. 2012; 4:452-458.
46. Mukamal KJ, Maclure M, Muller JE, Sherwood JB, 62. Tao L, Forester SC, Lambert JD. The role of the
Mittleman MA. Tea consumption and mortality after mitochondrial oxidative stress in the cytotoxic effects
acute myocardial infarction. Circulation. 2002; 105:2476- ofthe green tea catechin, (-)-epigallocatechin-3-gallate, in
2481. oral cells. Mol. Nutr. Food Res. 2014; 58:665-676.
47. Widlanski ME, Hamburg NM, Anter E, Holbrook M, 63. Calo LA, Vertolli U, Davis PA, Dal Maso L, Pagnin E,
Kahn DF, Elliott JG et al. Acute EGCG supplementation Ravarotto V et al. Molecular biology-based assessment
reverses endothelial dysfunction in patients with coronary of green tea effects on oxidative stress andcardiac
artery disease. J. Am. Coll. Nutr. 2007; 26:95-102. remodeling in dialysis patients. Clin. Nutr. 2014;
48. Ponzo V, Goitre I, Fadda M, Gambino R, De Francesco 33:437442.
A, Soldati L et al. Dietary flavonoid intake and 64. Vester H, Holzer N, Neumaier M, Lilianna S, Nüssler
cardiovascular risk: A population-based cohort study. J. AK, Seeliger C. Green tea extract (GTE)
Transl. Med. 2015; 13:218. improvesdifferentiation in human osteoblasts during
49. Serafini M, Del Rio D, Yao DN, Bettuzzi S, Peluso I. oxidative stress. J. Inflamm. (Lond.) 2014; 11:15.
Chapter 12: Health benefits of tea. In Herbal Medicine: 65. Sugita M, Kapoor MP, Nishimura A, Okubo T. Influence
Biomolecular, and Clinical Aspects, 2nd ed., CRC Press: of green tea catechins on oxidative stressmetabolites at
~ 70 ~
International Journal of Herbal Medicine http://www.florajournal.com
rest and during exercise in healthy humans. Nutrition Ogura S, Kozawa O et al. (Beta)-Epigallocatechin gallate
2016; 32:321-331. selectively inhibits adenosine diphosphate-stimulated
66. Jówko E, Sacharuk J, Balasinska B, Wilczak J, Charmas human platelet activation: Suppression of heat shock
M, Ostraszewski P et al. Effect of asingle dose of green protein 27 phosphorylation via p38 mitogen-activated
tea polyphenols on the blood markers of exercise-induced protein kinase. Mol. Med. Rep. 2014; 10:1383-1388.
oxidative stress in soccerplayers. Int. J. Sport Nutr. 81. Jain KS, Kathiravan MK, Somani RS, Shisloo CJ. The
Exerc. Metab. 2012; 22:486-496. biology and chemistry of hyperlipidemia. Bioorg. Med.
67. Zhao J, Fang S, Yuan Y, Guo Z, Zeng J, Guo Y et al. Chem. 2007; 15:4674-4699.
Green tea polyphenols protect spinalcord neurons against 82. Parthasarathy S, Raghavamenon A, Gareinabi MO,
hydrogen peroxide-induced oxidative stress. Neural Santanam N. Oxidized low-density lipoprotein. Methods
Regen. Res. 2014; 9:1379-1385. Mol. Biol. 2010; 610:403-417.
68. Jówko E, Długoł˛ecka B, Makaruk B, Cie´slinski I. The 83. Kim A, Chiu A, Barone MK, Avino D, Wang F, Coleman
effect of green tea extract supplements onexercise- CI, et al. Green tea catechins decrease total and low-
induced oxidative stress parameters in male sprinters. density lipoprotein cholesterol: A systematic review and
Eur. J Nutr. 2015; 54:783-791. meta-analysis. J. Am. Diet. Assoc. 2011; 111:1720-1729.
69. Bogdanski P, Suliburska J, Szulinska M, Stepien M, 84. Zheng XX, Xu YL, Li SH, Liu XX, Hui R, Huang XH.
Pupek-Musialik D, Jablecka A. Green tea extractreduces Green tea intake lowers fasting serum total and LDL
blood pressure, inflammatory biomarkers, and oxidative cholesterol in adults: A meta-analysis of 14 randomized
stress and improves parameters associatedwith insulin controlled trials. Am. J. Clin. Nutr. 2011; 94:601-610.
resistance in obese, hypertensive patients. Nutr. Res. 85. Wu AH, Spicer D, Stanczyk FZ, Tseng CC, Yang CS,
2012; 32:421-427. Pike MC. Effect of 2 month controlled green tea
70. Li M, Liu JT, Pang XM, Han CJ, Mao JJ. intervention on lipoprotein cholesterol, glucose, and
Epigallocatechin-3-gallate inhibits angiotensin II hormone levels in healthy postmenopausal women.
andinterleukin-6-induced C-reactive protein production Cancer Prev. Res. (Phila.) 2012; 5:393-402.
in macrophages. Pharmacol. Rep. 2012; 64:912-918. 86. Khalesi S, Sun J, Buys N, Jamashidi A, Nikbakht-
71. Guo Q, Zhao B, Shen S, Hou J, Hu J, Xin W. ESR study Nasrabadi E, Khosravi-Boroujeni H. Green tea catechins
on the structure–antioxidant activity relationship of tea and blood pressure: A systematic review and meta-
catechins and their epimers. Biochimica et Biophysica analysis of randomized controlled trials. Eur. J. Nutr.
Acta (BBA)-General Subjects. 1999; 1427(1):13-23. 2014; 53:1299-1311.
72. Senanayake SN. Green tea extract: Chemistry, 87. Ohmori R, Kondo K, Momiyama Y. Antioxidant
antioxidant properties and food applications–A review. beverages: Green tea intake and coronary artery disease.
Journal of Functional Foods. 2013; 5(4):1529-1541. Clin. Med. Insights Cardiol. 2014; 8(3):7-11.
73. Rice-Evans C. Implications of the mechanisms of action 88. Onakpoya I, Spencer E, Heneghan C, Thompson M. The
of tea polyphenols as antioxidants in vitro for effect of green tea on blood pressure and lipid profile: A
chemoprevention in humans. Proceedings of the Society systematic review and meta-analysis of randomized
for experimental Biology and Medicine. 1999; clinical trials. Nutr. Met. Cardiovasc. Dis. 2014; 24:823-
220(4):262-266. 836.
74. Tsai TH, Tsai TH, Chien YC, Lee CW, Tsai PJ. In vitro 89. Takechi R, Alfonso H, Hiramatsu N, Ishisaka A, Tanaka
antimicrobial activities against cariogenic streptococci A, Tan LB et al. Elevated plasma and urinary
and their antioxidant capacities: A comparative study of concentrations of green tea catechins associated with
green tea versus different herbs. Food Chemistry. 2008; improved plasma lipid profile in healthy Japanese
110(4):859-864. women. Nutr. Res. 2016; 36:220-226.
75. Bhardwaj P, Khanna D. Green tea catechins: Defensive 90. Tian C, Huang Q, Yang L, Légaré S, Angileri F, Yang H.
role in cardiovascular disorders. Chin. J. Nat. Med. 2013; Green tea consumption is associated with reduced
11:345-353. incident CHD and improved CHD-related biomarkers in
76. Son DJ, Cho MR, Jin YR, Kim SY, Park YH, Lee SH, et the Dongfeng-Tongji cohort. Sci. Rep. 2016; 6:24353.
al. Antiplatelet effect of green tea catechins: A possible 91. Suzuki-Sugihara N, Kishimoto Y, Saita E, Taguchi C,
mechanism through arachidonic acid pathway. Kobayashi M, Ichitani M et al. Green tea catechins
Prostaglandins Leukot. Essent. Fatty Acids. 2004; 71:25– prevent low-density lipoprotein oxidation via their
31. accumulation in low-density lipoprotein particles in
77. Jin YR, Im JH, Park ES, Cho MR, Han XH, Lee JJ et al. humans. Nutr. Res. 2016; 36:16-23.
Antiplatelet activity of epigallocatechin gallate is 92. Cushnie TT, Lamb AJ. Antimicrobial activity of
mediated by the inhibition of PLC2 phosphorylation, flavonoids. International Journal of Antimicrobial
elevation of PGD2 production, and maintaining calcium- Agents. 2005; 26(5):343-356.
ATPase activity. J. Cardiovasc. Pharmacol. 2008; 51:45- 93. Clercq E. New developments in anti-HIV chemotherapy.
54. Current Medicinal Chemistry. 2001; 8(13):1543-1572.
78. Ok WJ, Cho HJ, Kim HH, Lee DH, Kang HY et al. 94. Poole K. Overcoming antimicrobial resistance by
Epigallocatechin-3-gallate has an anti-platelet effect in a targeting resistance mechanisms. Journal of Pharmacy
cyclic AMP-dependent manner. J. Atheroscler. Thromb. and Pharmacology. 2001; 53(3):283-294.
2012; 19:337-348. 95. McNaught JG. On the action of cold or lukewarm tea on
79. Lee DH, Kim YJ, Kim HH, Cho HJ, Ryu JH, Rhee MH, Bacillus typhosus. Journal of the Royal Army Medical
et al. Inhibitory effects of epigallocatechin-3-gallate on Corps. 1906; 7(4):372-373.
microsomal cyclooxygenase-1 activity in platelets. 96. Taylor PW, Hamilton-Miller JM, Stapleton PD.
Biomol. Ther. 2013; 21:54-59. Antimicrobial properties of green tea catechins. Food
80. Iida Y, Doi T, Matsushima-Nishiwaki R, Tokuda H, Science and Technology bulletin. 2005; 2:71.
~ 71 ~
International Journal of Herbal Medicine http://www.florajournal.com
97. Dias TR, Tomás G, Teixeira NF, Alves MG, Oliveira PF, Iwasaki Y et al. The green tea polyphenol (-)-
Silva BM et al. White Tea (Camellia Sinensis (L.)): epigallocatechin gallate precipitates salivary proteins
Antioxidant Properties and Beneficial Health Effects. including alpha-amylase: Biochemical implications for
International Journal of Food Science, Nutrition and oral health. Eur. J. Oral Sci. 2012; 120:132-139.
Dietetics. 2013; 2(2):19-26. 115. Narotzki B, Levy Y, Aizenbud D, Reznick AZ. Green tea
98. Campos FM, Couto JA, Hogg TA. Influence of phenolic and its major polyphenol EGCG increase theactivity of
acids on growth and inactivation of Oenococcusoeni and oral peroxidases. Adv. Exp. Med. Biol. 2013; 756:99-
Lactobacillus hilgardii. Journal of Applied Microbiology. 104.
2003; 94(2):167-174. 116. Waltner-Law ME, Wang XL, Law BK, Hall RK, Nawano
99. Taguri T, Tanaka T, Kouno I. Antimicrobial activity of M, Granner DK. Epigallocatecin gallate, a constituent of
10 different plant polyphenols against bacteria causing green tea, represses hepatic glucose production. J Biol
food-borne disease. Biological and Pharmaceutical Chem. 2002; 277:34933-34940.
Bulletin. 2004; 27(12):1965-1969. 117. Wu LY, Juan CC, Hwang LS, Hsu YP, Ho PH, Ho LT.
100. Yam TS, Shah S, Hamilton-Miller JMT. Microbiological Green tea supplementation ameliorates insulin resistance
activity of whole and fractionated crude extracts of tea and increases glucose transporter IV content in a
(Camellia sinensis), and of tea components. FEMS fructose-fed rat model. Eur J Nutr. 2004; 43:116-124.
microbiology letters. 1997; 152(1):169-174. 118. Han MK. Epigallocatechin gallate, a constituent of green
101. Hara Y. Green tea: health benefits and applications. edn tea, suppresses cytokine-induced pancreatic beta-cell
1, CRC press, New York, 2001, 139-148. damage. Exp Mol Med. 2003; 35:136-139.
102. Negi PS, Jayaprakasha GK, Jena BS. Antioxidant and 119. Song EK, Hur H, Han MK. Epigallocatechin gallate
antimutagenic activities of pomegranate peel extracts. prevents autoimmune diabetes induced by multiple low
Food Chemistry 2003; 80(3):393-397. doses of streptozotocin in mice. Arch Pharm Res. 2003;
103. Gramza A, Korczak J. Tea constituents (Camellia 26:559-563.
sinensis L.) as antioxidants in lipid systems. Trends in 120. Kao YH, Chang HH, Lee MJ, Chen CL. Tea, obesity, and
Food Science & Technology 2005; 16(8):351-358. diabetes. Mol Nutr Food Res. 2006; 50(2):188-210.
104. Friedman M. Overview of antibacterial, antioxidant, 121. Shoji Y, Nakashima H. Glucose-lowering effect of
antiviral, and antifungal activities of tea flavonoids and powder formulation of African black tea extract in KK-
teas. Molecular Nutrition & Food Research. 2007; A(y)/TaJcl diabetic mouse. Arch Pharmacol Res. 2006;
51(1):116-134. 29(9):786-794.
105. He W, Li LX, Liao QJ, Liu CL, Chen XL. 122. Yang MH, Wang CH, Chen HL. Green, Oolong and
Epigallocatechin gallate inhibits HBV DNA synthesis in black tea extracts modulate lipid metabolism in
a viral replication-inducible cell line. World Journal of hyperlipidemia rats fed high-sucrose diet. J Nutr
Gastroenterology 2011; 17(11):1507. Biochem. 2001; 12:14-20.
106. Wang H, Xu J, Deng F, Hu Z. Natural extract of green 123. Klaus S, Pultz S, Thone-Reineke C, Wolfram S.
tea for inhibiting hepatitis B virus and its primary active Epigallocatechin gallate attenuates diet-induced obesity
ingredient. Faming Zhuanli Shenqing Gongkai in mice by decreasing energy absorption and increasing
Shuomingshu, CN 101028382, 2007, 9. fat oxidation. Int J Obes. 2005; 29(6):615-623.
107. Hamza A, Zhan CG. How can (-)-epigallocatechin gallate 124. Dulloo AG, Seydoux J, GirardierL, Chantre P,
from green tea prevent HIV-1 infection? Mechanistic Vandermander J. Green tea and thermogenesis:
insights from computational modeling and the interactions between catechin-polyphenols, caffeine and
implication for rational design of anti-HIV-1 entry sympathetic activity. Int J Obes Relat Metab Disord
inhibitors. The Journal of Physical Chemistry B. 2006; 2000; 24(2):252-258.
110(6):2910-2917. 125. Boschmann M, Thielecke F. The effects of
108. Matsumoto M, Mukai T, Furukawa S, Ohori H. epigallocatechin-3-gallate on thermogenesis and fat
Inhibitory effects of epigallocatechin gallate on the oxidation in obese men: a pilot study. J Am Coll Nutr
propagation of bovine coronavirus in Madin Darby 2007; 26(4):389S-395S.
bovine kidney cells. Animal Science Journal. 2005; 126. Samman S, Sandstrom B, Toft MB, Bukhave K, Jensen
76(5):507-512. M, Sorensen SS et al. Green tea or rosemary extract
109. Gaur S, Agnihotri R. Green tea: A novel functional food added to foods reduces nonheme-iron absorption. Am J
for the oral health of older adults. Geriatr. Gerontol. Int. Clin Nutr. 2001; 73:607-612.
2014; 14:238-250. 127. Nelson M, Poulter J. Impact of tea drinking on iron status
110. Awadalla HI, Ragab MH, Bassuoni MW, Fayed MT, in the UK: a review. J Hum Nutr Diet. 2004; 17:43-54.
Abbas MO. A pilot study of the role of green tea use on 128. Deng Z, Tao B, Li X, He J, Chen Y. Effect of green tea
oral health. Int. J. Dent. Hyg. 2011; 9:110-116. and black tea on the metabolisms of mineral elements in
111. Rassameemasmaung S, Phusudsawang P, Sangalungkarn old rats. Biol Trace Elem Res. 1998; 65:75-86.
V. Effect of green tea mouthwash on oral malodor. ISRN 129. Record IR, McInerney JK, Dreosti IE. Black tea, green
Prev. Med. 2012, 2013, 975148. tea, and tea polyphenols: effects on trace element status
112. Kushiyama M, Shimazaki Y, Murakami M, Yamashita Y. in weanling rats. Biol Trace Elem Res. 1996; 53:27-43.
Relationship between intake of green tea and periodontal 130. Mira L, Fernandez MT, Santos M, Rocha R, Florencio
disease. J. Periodontol. 2009; 80:372-377. MH, Jennings KR. Interactions of flavonoids with iron
113. Kato MT, Magalháes AC, Rios D, Hannas AR, Attin T, and copper ions: a mechanism fortheir antioxidant
Buzalaf MA. Protective effect of green tea on dentin activity. Free Radic Res. 2002; 36:1199-1208.
erosion and abrasion. J. Appl. Oral Sci. 2009; 17:560- 131. Maliakal PP, Coville PF, Wanwimolruk S. Tea
564. consumption modulates hepatic drug metabolizing
114. Hara K, Ohara M, Hayashi I, Hino T, Nishimura R, enzymes in Wistar rats. J Pharm Pharmacol 2001,
~ 72 ~
International Journal of Herbal Medicine http://www.florajournal.com
53:569-577.
132. Donovan JL, Crespy V, Manach C, Morand C, Besson C,
Scalbert A et al. Catechin is metabolized by both the
small intestine and liver of rats. J Nutr. 2001; 131:1753-
1757.
133. Embola CW, Weisburger JH, Weisburger MC. Urinary
excretion of N-OH-2- amino-3-methylimidazo [4, 5-
f]quinoline-N-glucuronide] in F344 rats is enhanced by
green tea. Carcinogenesis. 2001; 22:1095-1098.
134. Bruneton J. Pharmacognosie. Phytochimie. Plantes
Me’dicinales Paris: Technique Documentation-Lavoisier,
2001.
135. Costa LM, Gouveia ST, Nobrega JA. Comparison of
heating extraction procedures for Al, Ca, Mg and Mn in
tea samples. Ann Sci. 2002; 18:313-318.
136. Hamdaou MH, Chabchob S, Heidhili A. Iron
bioavailability and weight gains to iron-deficient rats fed
a commonly consumed Tunisian meal bean seeds ragout
with or without beef and with green or black tea
decoction. J Trace Elem Med Biol. 2003; 17:159-164.
137. Schmidt M, Schmitz HJ, Baumgart A, Guedon D, Netsch
MI, Kreuter MH et al. Toxicity of green tea extracts and
their constituents in rat hepatocytes in primary culture.
Food Chem Toxicol. 2005; 43:307-314.
138. Takabayashi F, Tahara S, Kanerko T, Harada N. Effect of
green tea catechins on oxidative DNA damage of hamster
pancreas and liver induced by Nnitrosobis (2-oxopropyl)
amine and/or oxidized soybean oil. Biofactors. 2004;
21:335-337.
139. Yun SY, Kim SP, Song DK. Effects of (-)-
epigallocatechin-3-gallate on pancreatic beta-cell damage
in streptozotocin-induced diabetic rats. Eur J Pharmacol
2006; 541:115-121.
140. Sakamoto Y, Mikuriya H, Tayama K, Takahashi H,
Nagasawa A, Yano N et al. Goitrogenic effects of green
tea extract catechins by dietary administration in rats.
Arch Toxicol. 2001; 75:591-596.
~ 73 ~