The prevention of cancer through dietary intervention is receiving considerable attention. Several epidemiological studies indicate that Green tea has a protective effect against a variety of malignant disorders such as lung cancer, breast cancer and prostate cancer. This preventive potential of green tea against cancer is attributed to the biologically active Flavonoids called catechins.
Green tea Catechins
Epigallocatechin 3-o-gallate,
EGCG, is the major catechin
found in green tea. Another catechin is GCG, gallocatechin-3-gallate.
Other catechins include epicatechin gallate (ECG), epigallocatechin (EGC),
and epichtechin (EC). The relative concentration of the five major tea catechins
are EGCG > ECG > EC > EGC > C.
Green Tea
Extract, 100 mg ( Yielding 35 mg EGCG ), 60 Tablets - Source Naturals

Green Tea Extract offers a convenient way to get the benefits of green
tea catechin EGCG in a highly concentrated green tea pill form. This green tea extract is standardized for
bioflavonoid-like antioxidants known as polyphenols, particularly (-)-Epigallocatechin
Gallate (EGCG). EGCG has been found in scientific studies to be a potent
antioxidant. Green tea antioxidants are likely to become more popular with time.
Green Tea
Supplement Facts
Green Tea Extract Yielding 70 mg EGCG catechin
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Research Update newsletter. Twice a month we email a brief abstract of
several studies on various supplements and natural medicine topics - including
benefit of green tea catechins - and
their practical interpretation by Ray Sahelian, M.D.
Suggested Use: 1
green tea catechin extract tablet a few times a week. Take green tea
catechin in the morning or midday
with a meal. Evening use may lead to mild insomnia.
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catechins
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Catechins and Cancer
Catechins exert diverse physiological effects against proliferative
diseases by several mechanisms, most of which are not completely
characterized.
Green Tea Catechins and
Prostate Cancer
Chemoprevention of human prostate cancer by oral administration of green
tea catechins in volunteers with high-grade prostate intraepithelial
neoplasia: a preliminary report from a one-year proof-of-principle study.
Cancer Res. 2006 Jan 15;66(2):1234-40. Department of Medicina
Sperimentale, Sezione di Biochimica, University of Parma, Via Volturno 39,
43100 Parma, Italy.
Recent studies showed that 30% of men with high-grade prostate
intraepithelial neoplasia (HG-PIN) would develop prostate cancer within 1
year after repeated biopsy. This prompted us to do a proof-of-principle
clinical trial to assess the safety and efficacy of green tea catechins
for the chemoprevention of prostate cancer in HG-PIN volunteers. The
purity and content of GTCs preparations were assessed by high-performance
liquid chromatography [(-)-epigallocathechin, 5%; (-)-epicatechin, 12%;
(-)-epigallocatechin-3-gallate, 51%; (-)-epicatechin-3-gallate, 6%; total
green tea catechins, 75%; caffeine, <1%]. Sixty volunteers with HG-PIN,
who were made aware of the study details, agreed to sign an informed
consent form and were enrolled in this double-blind, placebo-controlled
study. Daily treatment consisted of three green tea catechin capsules, 200
mg each (total 600 mg/d). After 1 year, only one tumor was diagnosed among
the 30 green tea catechins -treated men (incidence, approximately 3%),
whereas nine cancers were found among the 30 placebo-treated men
(incidence, 30%). Total prostate-specific antigen did not change
significantly between the two arms, but green tea catechins -treated men
showed values constantly lower with respect to placebo-treated ones.
International Prostate Symptom Score and quality of life scores of green
tea catechins -treated men with coexistent benign prostate hyperplasia
improved, reaching statistical significance in the case of International
Prostate Symptom Scores. No significant side effects or adverse effects
were documented. To our knowledge, this is the first study showing that
green tea catechins are safe and very effective for treating premalignant
lesions before prostate cancer develops. As a secondary observation,
administration of green tea catechins also reduced lower urinary tract
symptoms, suggesting that these compounds might also be of help for
treating the symptoms of benign prostate hyperplasia.
Catechins and Platelet
Aggregation
Complex effects of different green tea catechins on human platelets.
FEBS Lett. 2003 Jul 10;546(2-3):265-70. Institut fur Pharmakologie und
Klinische Pharmakologie, Universitatsklinikum Dusseldorf, Moorenstr 5,
D-40225 Dusseldorf, Germany.
Epigallocatechin gallate (EGCG), a major component of green tea, has been
previously shown to inhibit platelet aggregation. The effects of other
green tea catechins on platelet function are not known. Pre-incubation
with EGCG concentration-dependently inhibited thrombin-induced aggregation
and phosphorylation of p38 mitogen-activated protein kinase and
extracellular signal-regulated kinases-1/2. In contrast EGCG stimulated
tyrosine phosphorylation of platelet proteins, including Syk and SLP-76
but inhibited phosphorylation of focal adhesion kinase. Other catechins
did not inhibit platelet aggregation. Interestingly, when EGCG was added
to stirred platelets, a tyrosine kinase-dependent stimulation of platelet
aggregation was observed. The two other catechins containing a galloyl
group in the 3' position (catechin gallate, epicatechin gallate) also
stimulated platelet aggregation, while catechins without a galloyl group (catechin,
epicatechin) or the catechin with a galloyl group in the 2' position (epigallocatechin)
did not.
Catechin Research Update
Green tea extract and catechin ameliorate chronic fatigue-induced
oxidative stress in mice.
J Med Food. 2005 Spring;8(1):47-52.
Chronic fatigue syndrome (CFS) is an illness characterized by
persistent and relapsing fatigue, often accompanied by numerous symptoms
involving various body systems. The etiology of CFS remains unclear, but a
number of studies have shown that oxidative stress may be involved in its
pathogenesis. The present study was designed to investigate the protective
effect of green tea extract and catechin in the mouse model of CFS. Animals were
subjected to a forced swimming test session of 6 minutes every day for 7 days; a
significant increase in immobility time on successive days represented the CFS
in mice. Biochemical analysis revealed that the chronic swim test significantly
increased lipid peroxidation levels and decreased glutathione levels in mouse
whole-brain homogenate. Treatment with green tea extract (25 or 50 mg/kg, i.p.)
and catechin (50 or 100 mg/kg, i.p.) for 7 days reversed the increase in
immobility time. Protection was correlated with the lowered levels of lipid
peroxidation and restoration of reduced glutathione levels in the brains of
fatigued mice. These findings strongly suggest the pivotal role of oxidative
stress in the pathophysiology of CFS and that green tea extract and catechin
could be used as potential agents in the management of CFS and warrant the
inclusion of green tea extract and catechin in the treatment regimen of CFS
patients.
Catechins are the major source of flavonoids in a group of Australian women.
Asia Pac J Clin Nutr. 2004;13(Suppl):S72.
School of Public Health, Queensland University of Technology, Kelvin Grove, QLD
Australia.
Evidence is emerging for the role of flavonoids in the prevention
of degenerative diseases such as cancer and cardiovascular disease. Objective:
To determine the dietary intake of flavonoids in a group of Australian women.
Design: Twelve day weighed record data were available from 24 healthy young
women, participating in a larger study on diet and hormones; mean +/-SD age was
32.7+/-9.9 y and body mass index was 23.3+/-4.1 kg/m2. Dietary data were
analysed for intake of 15 individual flavonoids, comprising four major
subclasses: flavonols (quercetin, kaempferol, myricetin and fisetin), flavones (apigenin
and luteolin), flavanones (hesperetin, naringenin and eriodictyol) and flavanes
or catechins (epicatechin, epicatechin 3-gallate, epigallocatechin,
epigallocatechin 3-gallate, catechin, gallocatechin). As limited data are
available for the flavonoid content of Australian food and drink items, values
were mainly sourced from published international data; intake was estimated
utilising data for the aglycone form and for a limited number of glucosides
converted to aglycone equivalents. Results: Mean (SEM) daily intake in the group
was 25.6 mg/d for flavonols, 3.9+/- 0.7 mg/d for flavones, 22.6 +/- 4.9
mg/d for flavonones and 76.1+/-15.9 mg/d for catechins; total intake of
flavonoids was 128+/-19.9 mg/d. Major food sources in this group of women were:
onions, apples (with skin), tea (green, black), olives and broccoli, for
flavonols; fresh parsley and celery, for flavones; oranges, grapefruit and their
juices, for flavonones; and tea (green, black), apples (with or without skin),
red wine, dark chocolate and cocoa, for catechins. Conclusions: To our knowledge
these results are the first Australian data available on flavonoid intake.
Catechins were the major subclass of flavonoids in this group of women,
providing 59% of the total intake, followed by the flavonols (20%) and
flavonones (18%), and with a smaller contribution from the flavones (3%). Our
mean catechin intake was higher than that reported in Finnish (14.1 mg) or
American (25.4 mg/d) populations, and comparable to that in a Dutch population
(72 mg/d).