Green tea (Camellia sinensis), an evergreen shrub native to eastern Asia, is cultivated
extensively in India, China, Japan, Indonesia, Sri Lanka, Turkey, and Pakistan, as well as
other parts of the world, such as Africa and South America. The Chinese have used the
leaves to prepare beverages for over 4,000 years, believing that the tea infusion can cure
many diseases and prevent heart problems and cancer. Green tea also has been used to
flavor food, and the essential oil has been applied in perfumes and cosmetics.
Green tea is prepared from the steamed and dried leaves of the shrub. Different methods of
curing the leaves create different tea products. Black tea is produced by withering,
rolling, fermenting, and then drying the leaves. Oolong tea is semifermented and
considered an intermediate product between green and black tea.1,2
Tea was introduced to Europe in the 17th century and became a favorite beverage,
especially in the form of black tea. Today, almost two-thirds of the world’s
population consume tea in different forms (78% black, 20% green and 2% oolong). Green tea
is consumed mainly in Japan and China.3 Tea drinking in
Asian countries has evolved into a cultural habit and a part of everyday life.
Chemical Constituents
Several chemical constituents of green tea have been identified. The variation in chemical
composition is further complicated with fermentation and other treatments. The most
abundant components of green tea are polyphenols, such as gallic acid and catechin, and
their derivatives theogallin, gallocatechin, epiatechin, and epigallo catechin. The fresh
leaves contain 3%–4% caffeine (depending upon development), theobromine
(0.15%–0.2%), theophylline (0.02%–0.04%), and other methylxanthines.1 With
fermentation, catechins partially change into oligomeric quinones, including theaflavine,
theaflavine acid and thearubigene, or to the non-water-soluble flavonoids such as
quercetin, kaempferol and myrecetin.1,4,5 Green tea
contains B-vitamins and ascorbic acid, which are destroyed in the process of making black
tea. The essential oil contains more than 300 components including aldehydes, phenylethyl
alcohols, phenols, hexenal, hexenol, linalool, dihydroactinidiolide and p-vinylphenol.5
Physiologic Activity and Therapeutic Use
Freshly brewed green tea has an aroma with a slightly bitter taste. It stimulates the
nervous system and has a diuretic effect. Possible pharmacologic actions of green tea
include effects on lipid metabolism; antimicrobial, antioxidant, and antimutagenic
effects; and a wide variety of anticancer actions. In vitro and animal studies evoked high
hope that regular consumption of tea, especially green tea, would have a direct lowering
effect on plasma LDL levels. However, research has not supported such claims.
Antimutagenic and Anticarcinogenic Effects: Green tea has demonstrated
activity against various mutagens,6 and its
anticarcinogenic activities have been extensively examined. The polyphenol components of
green tea may possess chemopreventative properties. Their mechanisms of antimutagenesis
and anticarcinogenesis include the modulation of extracellular and intracellular metabolic
and proliferative processes.6,7 There is evidence that
induction of phase II enzymes glutathione-S-transferase and quinone reductase are enhanced
by nearly all tea fractions.8
Tea consumption has been shown to protect against chemical-induced stomach, lung,
esophagus, duodenum, pancreas, liver, breast and colon carcinogenesis in specific bioassay
models.6 A combination of curcumin (from the spice
turmeric) and the tea ingredient epigallocatechin-3 gallate proved to be even more
effective in inhibition of malignant human oral epithelial cells.9
Green tea extract exposure to human stomach cancer cells inhibited growth and induced
programmed cell death (apoptosis). These data suggest that green tea consumption may
protect humans from stomach cancer.10
Green tea and tea components were studied in the modulation of antitumor activity of
doxorubicin in mice with Erlich ascites tumors. The oral administration of green tea
extract enhanced the inhibitory effects of doxorubicin on tumor growth 2.5-fold.11 The results suggest that drinking green tea can positively
influence cancer chemotherapy.
Studies in mice showed that green tea inhibited chemical-induced hepatotoxicity.12 Naphthoquinone-induced hepatotoxicity was evaluated in rat
hepatocytes by measuring lactate dehydrogenase (LDH) leakage. Cell viability improved
after treatment with either tea extract or tea polyphenols. A mechanism of protection was
suggested to be closely related to the protein thiol content modulated by tea polyphenols.13
Clinical Studies: Epidemiological and human clinical studies produced
varying results. Most reported that green tea reduced risk of esophageal, pancreatic and
stomach cancer. However, a positive association between green tea consumption and
development of stomach and colon cancer also has been reported.14
In Japan, a large-scale study carried out from 1990 to 1995 included 1,706 histologically
diagnosed cases of digestive tract cancers and a total of 21,128 non-cancer outpatients.
High intake of green tea (7 or more cups/day) reduced the odds ratio of stomach cancer to
0.69 (95% confidence interval).15 Another study,
including 8,000 women, revealed that drinking 10 cups or more of green tea daily delayed
cancer onset. Stages I and II breast cancer patients who consumed 5 or more cups/day
experienced lower recurrence with longer disease-free period compared to occasional tea
drinkers.16 This indicates that consumption of green tea could play a role both in cancer
prevention and as an adjunct to chemotherapy.
The antibacterial effects of green tea against oral bacteria and several pathogenic
strains common in the GI tract also have been well documented. Green tea polyphenols
completely inhibited the growth and adherence of Porphyromonas gingivalis in a
concentration of 250–500 mcg/mL.17 After 5 minutes of contact, green tea polyphenol
solution (1 mg/mL) inhibited the proliferation of Streptococcus mutans.18
In general, green tea extracts proved to be bactericidal. They inhibited the growth of
diarrhea-causing Staphylococcus aureus, Staphylococcus epidermidis, Vibrio
parahaemolyticus, Campylobacter jejuni and Vibrio cholerae O1.19 The extracts also proved
effective against pathogenic methicillin-resistant S. aureus (MRSA) and, to some extent,
against penicillin-resistant S. aureus.20 In vitro tests
also showed that green tea was effective against some pathogenic fungi.21
The antioxidant activity of catechins has been studied in various experimental and human
conditions. It is now generally accepted that catechins possess antioxidant activity in
vitro and in vivo. Iron-induced oxidative stress was investigated in rat brains. Infusion
of green tea extract prevented oxidative injury induced by iron. Both iron-induced lipid
peroxidation products and iron-induced decrease in dopamine were suppressed.22
A Japanese longevity study suggested that regular green tea consumption could contribute
to an extended life span. More than 3,000 practitioners of chanoyu (Japanese tea ceremony)
were followed between 1980 and 1988. Their standardized mortality ratio was lower (0.55)
compared to that of the general Japanese female population (0.57).23
Other components of green tea, such as caffeine and tannin, can be effective in treating
different pathological conditions. Caffeine is an effective stimulant of the central
nervous system and can be useful in treating headaches and enhancing both stomach acid
production and renal excretion of water. Caffeine is frequently included in weight loss
pills and used as a cardiotonic agent.
Green tea also has been employed in cases of hepatitis, for protection of the liver
against chemical toxins, and (topically) in various skin disorders. Psoriasis and a number
of other common skin diseases are treated with psoralens combined with exposure to
ultraviolet A (PUVA). Although this treatment combination is highly effective, careful
follow-up cohort studies have shown that it greatly increases risk for the development of
cutaneous squamous cell carcinoma and melanoma.24 It has
been shown that green tea and constituent polyphenols protect against ultraviolet
B-induced carcinogenesis and reduce the growth rate of established tumors in the skin.
Zhao and coworkers showed that pre- and post-treatment with standardized green tea extract
abrogate PUVA-induced photochemical damage to skin.23
Precautions
Moderate consumption of green tea does not pose any hazard. However, women who are or
intend to become pregnant should avoid caffeine-containing products. Also, there is
evidence that highly condensed tannins and catechin could induce esophageal cancer.
Precaution is necessary in patients who are taking anticoagulants. It has been reported
that green tea may antagonize the effects of warfarin, an oral anticoagulant that requires
close monitoring to prevent complications.25 Tea combined
with milk may prevent the undesired effects of tannins. Patients with high blood pressure,
insomnia, asthma, heart conditions or elevated cholesterol should consult their physician
before becoming a regular tea drinker.
Dosage
The beneficial effects of tea infusion are typically seen at the dosages normally consumed
by humans. Overdose (quantities more than 300 mg caffeine, more than 5 cups/day) can lead
to negative effect on the CNS and irritation of the stomach.
Conclusion
Green tea is a popular beverage in Asia and is becoming recognized in the U.S. both as a
beverage and as an herbal remedy. Detailed multidisciplinary research on the effect of
green tea is available, and the following conclusions can be derived: 1) green tea
drinkers may enjoy a lower risk of developing certain cancers; 2) tea modifies oral and
intestinal microflora, reducing undesirable bacteria; 3) tea and tea polyphenols
selectively induce phase I and phase II enzymes, which may aid in detoxification of
harmful metabolites; and 4) the antioxidant effect of green tea may control inflammatory
processes, protect against DNA damage, and prolong life span.
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References
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- Bokuchava M, Skobeleva N. The biochemistry and technology of tea manufacture. Crit Rev Food Sci Nutr. 1980;12(4):303-370.
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- PDR for Herbal Medicine. Medical Economics Co, Montvale, NJ. First Edition. 1999; pp710.
- Duke J. Handbook of Medicinal Herbs. Boca Raton, FL. CRC Press 1985.
- Katiyar SK, Mukhtar H. Tea antioxidants in cancer prevention. J. Cell Biochem. (Suppl.) 1997;27:59-67.
- Facts and Comparisons, The Review of Natural Products. Green Tea, Feb., 1999.
- Steele VE, Kelloff GJ et al. Comparative mechanisms of green tea, black tea and selected polyphenols extracts measured in vitro bioassays. Carcinogenesis. 2000;21(1):63-67.
- Khafif A, Schanttz SP et al. Quantitation of chemopreventive synergism between (-)epigallocatechin-3-gallate and curcumin in normal, premalignant and malignant human oral epithelial cells. Carcinogenesis. 1998;19(3):419-424.
- Hibasami H, Komiya T, et al. Induction of apoptosis in human stomach cancer cells by green tea catechins. Oncol Rep. 1998;5(2):527-529.
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- Miyagawa C, Wu C, et al. Protective effect of green tea extract and tea polyphenols against the cytotoxicity of 1,4-naphtoquinone in isolated rat hepatocytes. Biosci Biotechnol Biochem. 1997;61(11):1901-1905.
- Bushman JL. Green tea and cancer in humans: a review of the literature. Nutr. Cancer. 1998;31(3):151-159.
- Inoue M., Tajima K. et al. Tea and coffee consumption and risk of digestive tract cancers: data from comparative case-referent study in Japan. Cancer Causes Control. 1998;9(2):209-216.
- Fujiki H. Two stages of cancer prevention with green tea. J Cancer Res Clin Oncol. 1999;125(11):589-597.
- Sakanaka S, Aizawa M, et al. Inhibitory effects of green tea polyphenols on growth and cellular adherence of an oral bacterium, Porphyromonas gingivalis. Biosci Biotechnol Biochem 1996;60(5):745-749.
- Saeki Y, Ito Y, et al. Antimicrobial action of green tea extract, flavono flavor and copper chlorophyll against oral bacteria. Bull Tokyo Dent Coll. 1993;34(1):33-37.
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- Lin AM, Chyi BY. The antioxidative property of green tea against iron-induced oxidative stress in rat brain. Chin J Physiology. 1998 Dec 31;41(4):189-194.
- Sadakata S, Fukao A, Hisamichi S. Mortality among female practitioners of Chanoyu (Japanese “tea ceremony”). Tohoku J Exp Med. 1992;166(4):475-477.
- Zhao JF, Zhang YJ, et al. Green tea protects against psoralen plus ultraviolet A-induced photochemical damage to skin. J Invest Dermatol 1999;113(6):1070-1075.
- Taylor JR, Wilt VM. Probable antagonism of warfarin by green tea. Ann Pharmacother. 1999;33(4):436-428.
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