Source: University of Mayland Medical Center
Also listed as: Camellia sinensis
Overview
Archeological evidence suggests that people consumed tea leaves steeped
in boiling water as many as 500,000 years ago. Botanical evidence
indicates that India and China were among the first countries to
cultivate tea. Today, hundreds of millions of people drink tea around
the world, and studies are now suggesting that green tea (Camellia
sinesis) in particular has many health benefits.
There are three main varieties of tea -- green, black, and oolong.
The difference between the teas is in their processing. Green tea is
made from unfermented leaves and reportedly contains the highest
concentration of powerful antioxidants called polyphenols. Antioxidants
are substances that scavenge free radicals -- damaging compounds in the
body that alter cells, tamper with DNA (genetic material), and even
cause cell death. Free radicals occur naturally in the body, but
environmental toxins (including ultraviolet rays from the sun,
radiation, cigarette smoke, and air pollution) also give rise to these
damaging particles. Scientists believe that free radicals contribute to
the aging process as well as the development of a number of health
problems including cancer and heart disease. Antioxidants such as
polyphenols in green tea can neutralize free radicals and may reduce or
even help prevent some of the damage they cause.
Green tea has been consumed throughout the ages in India, China,
Japan, and Thailand. In traditional Chinese and Indian medicine,
practitioners used green tea as a stimulant, diuretic (to promote the
excretion of urine), astringent (to control bleeding and help heal
wounds), and to improve heart health. Other traditional uses of green
tea include treating flatulence (gas), regulating body temperature and
blood sugar, promoting digestion, and improving mental processes.
Green tea has been extensively studied in people, animals, and
laboratory experiments. Results from these studies suggest that green
tea may be useful for the following health conditions:
Atherosclerosis
Population-based studies indicate that the antioxidant properties of
green tea may help prevent atherosclerosis, particularly coronary
artery disease. (Population-based studies means studies that follow
large groups of people over time and/or studies that are comparing
groups of people living in different cultures or with different dietary
habits, etc.) In May 2006, however, the U.S. Food and Drug
Administration (FDA) rejected a petition from teamakers to allow tea
labels to claim that green tea reduces the risk of heart disease. The
FDA concluded that there is no credible evidence to support qualified
health claims for green tea or green tea extract reducing the risk
of heart disease.
High cholesterol
Research shows that green tea lowers total cholesterol and raises
HDL ("good") cholesterol in both animals and people. One
population-based study found that men who drink green tea are more
likely to have lower total cholesterol than those who do not drink
green tea. Results from one animal study suggest that polyphenols in
green tea may block the intestinal absorption of cholesterol and
promote its excretion from the body. In another small study of male
smokers, researchers found that green tea significantly reduced blood
levels of harmful LDL cholesterol.
Cancer
Several population-based studies have shown that green tea helps
protect against cancer. For example, cancer rates tend to be low in
countries such as Japan where people regularly consume green tea.
However, it is not possible to determine from these population-based
studies whether green tea actually prevents cancer in people. Emerging
studies suggest that the polyphenols in green tea may play an important
role in the prevention of cancer. Researchers also believe that
polyphenols help kill cancerous cells and stop their progression.
Bladder cancer. Only a few studies have examined the
relationship between bladder cancer and green tea consumption. In one
study that compared people with and without bladder cancer, researchers
found that women who drank black tea and powdered green tea were less
likely to develop bladder cancer. A follow-up study by the same group
of researchers revealed that bladder cancer patients (particularly men)
who drank green tea had a substantially better 5-year survival rate
than those who did not.
Breast cancer. Studies in animals and test tubes suggest that
polyphenols in green tea inhibit the growth of breast cancer cells. In
one study of 472 women with various stages of breast cancer,
researchers found that women who consumed the most green tea
experienced the least spread of cancer (particularly premenopausal
women in the early stages of breast cancer). They also found that women
with early stages of the disease who drank at least 5 cups of tea every
day before being diagnosed with cancer were less likely to suffer
recurrences of the disease after completion of treatment. However,
women with late stages of breast cancer experienced little or no
improvement from drinking green tea. In terms of breast cancer
prevention, the studies are inconclusive. In one very large study from
Japan, researchers found that drinking green tea was not associated
with a reduced risk of breast cancer.
Ovarian cancer. In a study conducted on ovarian cancer
patients in China, researchers found that women who drank at least one
cup of green tea per day survived longer with the disease than those
who didn’t drink green tea. In fact, those who drank the most tea,
lived the longest.
Colorectal cancer. Studies on the effects of green tea
on colon or rectal cancer have produced conflicting results. Some
studies show decreased risk in those who drink the tea, while others
show increased risk. Further research is needed before researchers can
recommend green tea for the prevention of colorectal cancer.
Esophageal cancer. Studies in laboratory animals have
found that green tea polyphenols inhibit the growth of esophageal
cancer cells. However, studies in people have produced conflicting
findings. For example, one large-scale population-based study found
that green tea offered significant protection against the development
of esophageal cancer (particularly among women). Another
population-based study revealed just the opposite -- green tea
consumption was associated with an increased risk of esophageal cancer.
In fact, the stronger and hotter the tea, the greater the risk. Given
these conflicting results, further research is needed before scientists
can recommend green tea for the prevention of esophageal cancer.
Lung cancer. While green tea polyphenols have been shown
to inhibit the growth of human lung cancer cells in test tubes, few
studies have investigated the link between green tea consumption and
lung cancer in people and even these studies have been conflicting. One
population-based study found that Okinawan tea (similar to green tea
but partially fermented) was associated with decreased lung cancer
risk, particularly among women. A second study revealed that green tea
and black tea significantly increased the risk of lung cancer. As with
colon and esophageal cancers, further studies are needed before
researchers can draw any conclusions about green tea and lung cancer.
Pancreatic cancer. In one large-scale study researchers
compared green tea drinkers with non-drinkers and found that those who
drank the most tea were significantly less likely to develop pancreatic
cancer. This was particularly true for women -- those who drank the
most green tea were half as likely to develop pancreatic cancer as
those who drank less tea. Men who drank the most tea were 37% less
likely to develop pancreatic cancer. However, it is not clear from this
population-based study whether green tea is solely responsible for
reducing pancreatic cancer risk. Further studies in animals and people
are needed before researchers can recommend green tea for the
prevention of pancreatic cancer.
Prostate cancer. Laboratory studies have found
that green tea extracts prevent the growth of prostate cancer cells in
test tubes. In a large study conducted in Southeast China researchers
found that the risk of prostate cancer declined with increasing
frequency, duration and quantity of green tea consumption. However,
both green and black tea extracts also stimulated genes that cause
cells to be less sensitive to chemotherapy drugs. Given this potential
interaction, people should not drink black and green tea (as well as
extracts of these teas) while receiving chemotherapy.
Skin cancer. The main polyphenol in green tea is
epigallocatechin gallate (EGCG). Scientific studies suggest that EGCG
and green tea polyphenols have anti-inflammatory and anti-cancer
properties that may help prevent the onset and growth of skin tumors.
Stomach cancer. Laboratory studies have found that green
tea polyphenols inhibit the growth of stomach cancer cells in test
tubes, but studies in people have been less conclusive. In two studies
that compared green tea drinkers with non-drinkers, researchers found
that people who drank tea were about half as likely to develop stomach
cancer and gastritis (inflammation of the stomach) as those who did not
drink green tea. However, a study including more than 26,000 men and
women in Japan found no association between green tea consumption and
stomach cancer risk. Some studies even suggest that green tea may
increase the risk of stomach cancer.
Further studies are underway to determine whether green tea helps
reduce the risk of stomach cancer. Although green tea is considered
safe for people at risk for stomach cancer, it is too soon to tell
whether green tea reduces the likelihood of developing this disease.
Inflammatory Bowel Disease (IBD)
Green tea may help reduce inflammation associated with Crohn's
disease and ulcerative colitis, the two types of IBD. If green tea
proves to be helpful for preventing colon cancer, this would be an
added benefit for those with IBD because they are at risk for colon
cancer.
Diabetes
Green tea has been used traditionally to control blood sugar in the
body. Animal studies suggest that green tea may help prevent the
development of type 1 diabetes and slow the progression once it has
developed. People with type 1 diabetes produce little or no insulin, a
hormone that converts glucose (sugar), starches, and other foods into
energy needed for daily life. Green tea may help regulate glucose in
the body.
Liver disease
Population-based studies have shown that men who drink more than 10
cups of green tea per day are less likely to develop disorders of the
liver. Green tea also seems to protect the liver from the damaging
effects of toxic substances such as alcohol. Animal studies have shown
that green tea helps protect against the development of liver tumors in
mice.
Results from several animal and human studies suggest that one of
the polyphenols present in green tea, known as catechin, may help treat
viral hepatitis (inflammation of the liver from a virus). In these
studies, catechin was isolated from green tea and used in very high
concentrations. It is not clear whether green tea (which contains a
lower concentration of catechins) confers these same benefits to people
with hepatitis.
Weight loss
Studies suggest that green tea extract may boost metabolism and help
burn fat. One study confirmed that the combination of green tea and
caffeine improved weight loss and maintenance in overweight and
moderately obese individuals. However, a second study found that weight
maintenance following weight loss was not affected by green tea. Some
researchers speculate that substances in green tea known as
polyphenols, specifically the catechins, are responsible for the herb's
fat-burning effect.
Plant Description
Green, black, and oolong tea are all derived from the leaves of the Camellia sinensis plant. Originally cultivated in East Asia, this plant grows as large as a shrub or tree. Today, Camellia sinensis grows throughout Asia and parts of the Middle East and Africa.
People in Asian countries more commonly consume green and oolong tea
while black tea is most popular in the United States. Green tea is
prepared from unfermented leaves, the leaves of oolong tea are
partially fermented, and black tea is fully fermented. The more the
leaves are fermented, the lower the polyphenol content ( see: What's It Made Of? ), and the higher the caffeine content. Green tea has the highest
polyphenol content while black tea has roughly two to three times the
caffeine content of green tea.
What's It Made Of?
The healthful properties of green tea are largely attributed to
polyphenols, chemicals with potent antioxidant properties. In fact, the
antioxidant effects of polyphenols appear to be greater than vitamin C.
The polyphenols in green tea also give it a somewhat bitter flavor.
Polyphenols contained in teas are classified as catechins. Green tea
contains six primary catechin compounds: catechin, gallaogatechin,
epicatechin, epigallocatechin, epicatechin gallate, and
apigallocatechin gallate (also known as EGCG). EGCG is the most studied
polyphenol component in green tea and the most active.
Green tea also contains alkaloids including caffeine, theobromine,
and theophylline. These alkaloids provide green tea's stimulant
effects.
Available Forms
Most green tea products are sold as dried leaf tea. There are also
extracts made from the leaves and leaf buds. The average cup of green
tea contains between 50 to 150 mg polyphenols. Decaffeinated green tea
products contain concentrated polyphenols. Capsules and liquid
preparations are also available.
How to Take It
Pediatric
There are no known scientific reports on the pediatric use of green tea, so it is not currently recommended for children.
Adult
Depending on the brand, two to three cups of green tea per day (for
a total of 240 to 320 mg polyphenols) or 300 to 400 mg per day of
standardized green tea extract is the recommended dosage.
Precautions
The use of herbs is a time-honored approach to strengthening the
body and treating disease. However, herbs contain active substances
that can trigger side effects and interact with other herbs,
supplements, or medications. For these reasons, people should take
herbs with care, under the supervision of a practitioner knowledgeable
in the field of botanical medicine.
People with heart problems, kidney disorders, stomach ulcers, and
psychological disorders (particularly anxiety) should not take green
tea. Pregnant and breastfeeding women should also avoid green tea.
People who drink excessive amounts of caffeine (including caffeine
from green tea) for prolonged periods of time may experience
irritability, insomnia, heart palpitation, and dizziness. Caffeine
overdose can cause nausea, vomiting, diarrhea, headaches, and loss of
appetite. If you are drinking a lot of tea and start to vomit or have
abdominal spasms, you may have caffeine poisoning. Lower your caffeine
intake and see your healthcare provider if your symptoms are severe.
Possible Interactions
If you are currently being treated with any of the following
medications, you should not drink green tea or take green tea extract
without first talking to your doctor:
Adenosine. Green tea may inhibit the actions of adenosine, a
medication administered in a hospital setting for an irregular (and
usually unstable) heart rhythm.
Antibiotics, beta-lactam. Green tea may increase the effectiveness of beta-lactam antibiotics by reducing bacterial resistance to treatment.
Aspirin. Green tea and aspirin should not be mixed because
they both prevent platelets from clotting. Using the two together may
increase your risk of bleeding.
Benzodiazepines. Caffeine (including caffeine from green
tea) has been shown to reduce the sedative effects of benzodiazepines
(medications commonly used to treat anxiety, such as diazepam and
lorazepam).
Beta-blockers, propranolol and metoprolol. Caffeine
(including caffeine from green tea) may increase blood pressure in
people taking propranolol and metoprolol (medications used to treat
high blood pressure and heart disease).
Blood Thinning Medications . People who take warfarin, a blood thinning
medication, should not drink green tea. Since green tea contains
vitamin K, it can make warfarin ineffective. (See also the aspirin
listing, above.)
Chemotherapy. The combination of green tea and chemotherapy
medications, specifically doxorubicin and tamoxifen, increased the
effectiveness of these medications in laboratory tests. However, these
results have not yet been demonstrated in studies on people. On the
other hand, there have been reports of both green and black tea
extracts stimulating a gene in prostate cancer cells that may cause
them to be less sensitive to chemotherapy drugs. Given this potential
interaction, people should not drink black and green tea (as well as
extracts of these teas) while receiving chemotherapy for prostate
cancer in particular.
Clozapine. The anti-psychotic effects of the medication clozapine may be reduced if taken less than 40 minutes after drinking green tea.
Ephedrine. When taken together with ephedrine, green tea may cause agitation, tremors, insomnia, and weight loss.
Lithium. Green tea has been shown to reduce blood levels of lithium (a medication used to treat manic/depression).
Monoamine oxidase inhibitors (MAOIs). Green tea may cause a
severe increase in blood pressure (called a "hypertensive crisis") when
taken together with MAOIs used to treat depression. Examples of MAOIs
include phenelzine and tranylcypromine.
Oral contraceptives. Oral contraceptives can prolong the amount of time caffeine stays in the body and may increase its stimulating effects.
Phenylpropanolamine. A combination of caffeine (including
caffeine from green tea) and phenylpropanolamine (an ingredient used in
many over-the-counter and prescription cough and cold medications and
weight loss products) can cause mania and a severe increase in blood
pressure. The FDA issued a public health advisory in November 2000 to
warn people of the risk of bleeding in the brain from use of this
medication and has strongly urged all manufacturers of this drug to
remove it from the market.
Supporting Research
Alic M. Green tea for remission maintenance in Crohn's disease? Am J Gastroenterol. 1999;94(6):1710.
Blumenthal M, ed. The Complete German Commission E Monographs. Therapeutic Guide to Herbal Medicines . Boston, Mass: Integrative Medicine Communications; 1998:47, 132.
Borrelli F, Capasso R, Russo A, Ernst E. Systematic review: green tea and gastrointestinal cancer risk. Aliment Pharmacol Ther Mar 1, 2004;19(5):497-510.
Brinker F. Herb Contraindications and Drug Interactions. 2nd ed. Sandy, OR: Eclectic Medical Publications; 1998:126-129.
Brown MD. Green tea (Camellia sinensis) extract and its possible role in the prevention of cancer. Alt Med Rev . 1999;4(5):360-370.
Bushman JL. Green tea and cancer in humans: a review of the literature. Nutr Cancer . 1998;31(3):151-159.
Craig WJ. Health-promoting properties of common herbs. Am J Clin Nutr . 1999;70(suppl):491S-499S.
Dulloo AG, Duret C, Rohrer D, et al. Efficacy of a green tea extract
rich in catechin polyphenols and caffeine in increasing 24-h energy
expenditure and fat oxidation in humans. Am J Clin Nutr . 1999;70:1040-1045.
Ernst E, ed. The Desktop Guide to Complementary and Alternative Medicine: An Evidence-Based Approach . Mosby, Edinburgh; 2001:119-121.
Ernst E, Cassileth BR. How useful are unconventional cancer treatments? Eur J Cancer . 1999;35(11):1608-1613.
Fujiki H, Suganuma M, Okabe S, et al. Cancer inhibition by green tea. Mutation Research. 1998;307-310.
Fujiki H, Suganuma M, Okabe S, et al. Mechanistic findings of green tea as cancer preventive for humans. Proc Soc Exp Biol Med . 1999;220(4):225 – 228.
Gao Yt, McLaughlin JK, Blot WJReduced risk of esophageal cancer associated with green tea consumption. J Natl Cancer Inst. 1994 Jun 1;86(11):855-8.
Geleijnse JM, Launer LJ, Hofman A, Pols HA, Witteman JCM. Tea
flavonoids may protect against atherosclerosis: the Rotterdam study. Arch Intern Med. 1999;159:2170-2174.
Gomes A, Vedasiromoni JR, Das M, Sharma RM, Ganguly DK. Anti-hyperglycemic effect of black tea (Camellia sinensis) in rat. J Ethnopharmocolgy . 1995;45:223-226.
Gruenwalkd J, Brendler T, Jaenicke C, scientific eds; Fleming T, chief ed. PDR for Herbal Medicines . 2nd ed. Montvale, NJ:Medical Economics Company; 2000:369-372.
Heck AM, DeWitt BA, Lukes AL. Potential interactions between alternative therapies and warfarin. [review]. Am J Health Syst Pharm . 2000 Jul 1;57(13):1221-1227.
Hu J, Nyren O, Wolk A, Bergstrom R, et al. Risk factors for oesophageal cancer in northeast China. Int J Cancer . 1994;57(1):38-46.
Imai K, Suga K, Nagachi K. Cancer-preventive effects of drinking green tea among a Japanese population. Prev Med . 1997;26(6):769-775.
Inoue M, Tajima K, Mizutani M, et al. Regular consumption of green tea
and the risk of breast cancer recurrence: follow-up study from the
Hospital-based Epidemiologic Research Program at Aichi Cancer Center
(HERPACC), Japan. Cancer Lett . 2001;167(2):175-182.
Ji B-T, Chow W-H, Hsing AW, et al. Green tea consumption and the risk of pancreatic and colorectal cancers. Int J Cancer . 1997;70:255-258.
Jian L, Xie LP, Lee AH, Binns CW. Protective effect of green tea
against prostate cancer: a case-control study in southeast China. Int J Cancer Jan 1, 2004;108(1):130-135.
Kaegi E. Unconventional therapies for cancer: 2. Green tea. [Review].
The Task Force on Alternative Therapies of the Canadian Breast Cancer
Research Initiative. CMAJ . 1998;158(8):1033-1035.
Katiyar SK, Ahmad N, Mukhtar H. Green tea and skin. Arch Dermatol . 2000;136(8):989-94.
Katiyar SK, Mukhtar H. Tea antioxidants in cancer chemoprevention. [Review]. J Cell Biochem Suppl . 1997;27:59-67.
Kono S, Shinchi K, Ikeda N, Yanai F, Imanishi K. Green tea consumption
and serum lipid profiles: a cross-sectional study in northern Kyushu,
Japan. Prev Med . 1992 Jul;21(4):526-531.
Kovacs EM, Lejeune MP, Nijs I, Westerterp-Plantenga MS. Effects of green tea on weight maintenance after body-weight loss. Br J Nutr Mar 1, 2004;91(3):431-437.
Kuroda Y, Hara Y. Antimutagenic and anticarcinogenic activity of tea polyphenols. [Review]. Mutat Res . 1999;436(1):69-97.
Lee W, Min WK, Chun S, Lee YW, Park H, Lee do H, Lee YK, Son JE.
Long-term effects of green tea ingestion on atherosclerotic biological
markers in smokers. Clin Biochem . Jan 1, 2005;38(1):84-87.
Low Dog T, Riley D, Carter T. Traditional and alternative therapies for breast cancer. Alt Ther . 2001;7(3):36-47.
Luo M, Kannar K, Wahlqvist ML, O'Brien RC. Inhibition of LDL oxidation by green tea extract. Lancet . 1997 Feb 1;349(9048):360-361.
Luper S. A review of plants used in the treatment of liver disease: part two. Alt Med Rev . 1999;4(3):178-188.
Lyn-Cook BD, Rogers T, Yan Y, Blann EB, Kadlubar FF, Hammons GJ.
Chemopreventive effects of tea extracts and various components on human
pancreatic and prostate tumor cells in vitro. Nutr Cancer . 1999;35(1):80-86.
McKenna DJ, Hughes K, Jones K. Green tea monograph. Alt Ther . 2000;6(3):61-84.
Miura Y, Chiba T, Tomita I, et al. Tea catechins prevent the development of atherosclerosis in apoprotein E-deficient mice. J Nutr . 2001;131(1):27-32.
Mukhtar H, Ahmad N. Green tea in chemoprevention of cancer. [Review]. Toxicol Sci. 1999;52(2 Suppl):111-117.
Nakachi K, Suemasu K, Suga K, Takeo T, Imai K, Higashi Y. Influence of
drinking green tea on breast cancer malignancy among Japanese patients. Jpn J Cancer Res . 1998;89(3):254-261.
Nagata C, Kabuto M, Shimizu H. Association of coffee, green tea, and
caffeine intakes with serum concentrations of estradiol and sex hormone
– binding globulin in premenopausal Japanese women. Nutr Cancer . 1998;30(1):21 – 24.
Ohno Y, Aoki K, Obata K, Morrison AS. Case-control study of urinary bladder cancer in metropolitan Nagoya. Natl Cancer Inst Monogr . 1985;69:229-234.
Ohno Y, Wakai K, Genka K, et al. Tea consumption and lung cancer risk: a case-control study in Okinawa, Japan. Jpn J Cancer Res . 1995;86(11):1027-1034.
Pianetti S, Guo S, Kavanagh KT, Sonenshein GE. Green tea polyphenol
epigallocatechin-3 gallate inhibits Her-2/neu signaling, proliferation,
and transformed phenotype of breast cancer cells. Cancer Res . 2002;62(3):652-655.
Picard D. The biochemistry of green tea polyphenols and their potential application in human skin cancer. Altern Med Rev . 1996;1(1):31-42.
Robbers JE, Tyler VE. Tyler's Herbs of Choice . New York: The Haworth Herbal Press; 1999: 249-250.
Sadzuka Y, Sugiyama T, Hirota. Modulation of cancer chemotherapy by green tea. Clin Cancer Res . 1998;4(1):153 – 156.
Sano T, Sasako M. Green tea and gastric cancer. N Engl J Med . 2001;344(9):675-676.
Sasazuki S, Kodama H, Yoshimasu K et al. Relation between green tea
consumption and the severity of coronary atherosclerosis among Japanese
men and women. Ann Epidemiol . 2000;10:401-408.
Setiawan VW, Zhang ZF, Yu GP, et al. Protective effect of green tea on the risks of chronic gastritis and stomach cancer. Int J Cancer . 2001;92(4):600-604.
Shim JH, Kang MG, Kim YH, Roberts C, Lee IP. Chemopreventive effect of green tea (Camellia sinensis) among cigarette smoke. Cancer-Epidemio-Biomarkers-Prev . 1995;Jun; 4(4): 387-91.
Shiota S, Shimizu M, Mizushima T, Ito H, et al. Marked reduction in the
minimum inhibitory concentration (MIC) of ß-lactams in
methicillin-resistant Staphylococcus aureus produced by epicatechin
gallate, an ingredient of green tea (Camellia sinensis). Biol. Pharm. Bull . 1999;22(12):1388-1390.
Suganuma M, Okabe S, Kai Y, Sueoka N, et al. Synergistic effects of
(-)-epigallocatechin gallate with (-)-epicatechin, sulindac, or
tamoxifen on cancer-preventive activity in the human lung cancer cell
line PC-9. Cancer Res . 1999;59:44-47.
Suganuma M, Okabe S, Sueoka N, et al. Green tea and cancer chemoprevention. Mutat Res . 1999 Jul 16;428(1-2):339-344.
Sugiyama T, Sadzuka Y. Combination of theanine with doxorubicin inhibits hepatic metastasis of M5076 ovarian sarcoma. Clin Cancer Res . 1999;5:413-416.
Sugiyama T, Sadzuka Y. Enhancing effects of green tea components on the
antitumor activity of adriamycin against M5076 ovarian sarcoma. Cancer Lett . 1998;133(1):19 – 26.
Suzuki Y, Tsubono Y, Nakaya N, Suzuki Y, Koizumi Y, Tsuji I. Green tea
and the risk of breast cancer: pooled analysis of two prospective
studies in Japan. Br J Cancer . Apr 5, 2004;90(7)1361-1363.
Taylor JR, Wilt VM. Probable antagonism of warfarin by green tea. Ann Pharmacother. 1999;33(4):426 – 428.
Tewes FJ, Koo LC, Meisgen TJ, Rylander R. Lung cancer risk and mutagenicity of tea. Environ Res . 1990;52(1):23-33.
Thatte U, Bagadey S, Dahanukar S. Modulation of programmed cell death by medicinal plants. [Review]. Cell Mol Biol . 2000;46(1):199-214.
Tsubono Y, Nishino Y, Komatsu S, et al. Green tea and the risk of gastric cancer in Japan. N Engl J Med . 2001;344(9):632-636.
van het Hof KH, de Boer HS, Wiseman SA, Lien N, Westrate JA, Tijburg
LB. Consumption of green or black tea does not increase resistance of
low-density lipoprotein to oxidation in humans. Am J Clin Nutr . 1997 Nov;66(5):1125-1132.
Wakai K, Ohno Y, Obata K, Aoki K. Prognostic significance of selected lifestyle factors in urinary bladder cancer. Jpn J Cancer Res . 1993 Dec;84(12):1223-1229.
Wang Z, et al. Antimutagenic activity of green tea polyphenols. Mutation Research. 1989;223:273 – 285.
Wargovich MJ, Woods C, Hollis DM, Zander ME. Herbals, cancer prevention and health. [Review]. J Nutr . 2001;131(11 Suppl):3034S-3036S.
Wei H, Zhang X, Zhao JF, Wang ZY, Bickers D, Lebwohl M. Scavenging of
hydrogen peroxide and inhibition of ultraviolet light-induced oxidative
DNA damage by aqueous extracts from green and black teas. Free Radic Biol Med . 1999;26(11-12):1427-1435.
Weisburger JH. Tea and health: a historic perspective. Cancer Letters . 1997;114:315-317.
Westerterp-Plantenga MS, Lejeune MP, Kovacs EM. Body weight and weight
maintenance in relation to habitual caffeine intake and green tea. Obes Res Jul 2005;13(7):1195-1204.
Windridge C. The Fountain of Health. An A-Z of Traditional Chinese Medicine . London, England: Mainstream Publishing; 1994:259.
Yamane T, Nakatani H, Kikuoka N, et al. Inhibitory effects and toxicity
of green tea polyphenols for gastrointestinal carcinogenesis. Cancer . 1996;77(8 Suppl):1662-1667.
Yang TT, Koo MW. Hypocholesterolemic effects of Chinese tea. Pharmacol Res . 1997;35(6):505-512.
Yang TTC, Koo MWI. Chinese green tea lowers cholesterol level through an increase in fecal lipid excreiton. Life Sciences . 1999:66:5:411-423.
Yu GP, Hsieh CC, Wang LY, Yu SZ, Li XL, Jin TH. Green-tea consumption
and risk of stomach cancer: a population-based case-control study in
Shanghai, China. Cancer Causes Control. 1995;6(6):532-538.
Zhang M, Lee AH, Binns CW, Xie X. Green tea consumption enhances survival of epithelial ovarian cancer. Int J Cancer Nov 10, 2004;112(3):465-469.
- Review Date:
9/30/2005
- Reviewed By: Amy Paturel, MS, MPH. Previously reviewed by:
Jacqueline A. Hart, MD, Department of Internal Medicine,
Newton-Wellesley Hospital, Harvard University and Senior Medical Editor
Integrative Medicine, Boston, MA; Gary Kracoff, RPh (Pediatric Dosing
section February 2001), Johnson Drugs, Natick, MA; Steven Ottariono,
RPh, Veteran's Administrative Hospital, Londonderry, NH. All
interaction sections have also been reviewed by a team of experts
including Joseph Lamb, MD (July 2000), The Integrative Medicine Works,
Alexandria, VA;Enrico Liva, ND, RPh (August 2000), Vital Nutrients,
Middletown, CT; Brian T Sanderoff, PD, BS in Pharmacy (March 2000),
Clinical Assistant Professor, University of Mayland School of
Pharmacy; President, Your Prescription for Health, Owings Mills, MD; R.
Lynn Shumake, PD (March 2000), Director, Alternative Medicine
Apothecary, Blue Mountain Apothecary & Healing Arts, University of Mayland Medical Center, Glenwood, MD; Ira Zunin, MD, MPH, MBA (July
2000), President and Chairman, Hawaii State Consortium for Integrative
Medicine, Honolulu, HI.
Statements made on this site has not been evaluated by the Food and Drug Administration.Energyade is not intended to diagnose, treat or cure or prevent a disease. Information on this site provided for eductional purposes only. The information provided herein should not be used during any
medical emergency or for the diagnosis or treatment of any medical
condition or disease. A licensed medical professional should be consulted for
diagnosis and treatment of any and all medical conditions. Call 911 for
all medical emergencies. Links to other sites are provided for
information purposes only -- they do not constitute endorsements of those other
sites.
|