good health co
Good Health Group of America, LLC
Healthy Day Essentials™
Search:
About Us
Products A-Z
Contact Us
Site Map
View Cart
Glossary
Health News
FAQs
Jump to:

Home
Acai Berry
Adults Over 50
Aging Marks
Alcoholism
Alertness
Allergies
Alzheimer’s Disease
Amino Acids
Anti-Aging
Anti-Inflammatory
Anti-Oxidant
Anxiety
Appetite Suppression
Arthersclorosis
Arthritis

ATP

Bilberry
Bladder Cancer
Bladderwrack
Bloating
Blood Pressure
Blood Sugar
Bone Health
Brain Boosters
Broccoli Powder
Breast Cancer
Bromelain
Calcium
Cancer
Cardio-Health
Carpal Tunnel
Cataract
Cha de Bugre
Children’s Health
Cholesterol Health
Chondroitin
Chromium
CLA
Co-Enzyme Q-10
Cognitive / CNS Health
Colon & Rectal Support
Common Cold
Concentration
Constipation
Damaged cells
Dental Cavities
Depression
Detox
Devil's Claw
DHEA Plus
Diabetes
Digestion
Echinacea
Eczema
Energy
Erectile Dysfunction
Estrogen Therapy
Evening Primrose Oil
Eye Health
Fat Burning
Fatigue
Female Super Pack
Fertility Therapy
Fibromyalgia Support
Flax Seed Oil
Folic Acid
Fruits & Berries
GABA
Garlic
GI Support
Ginkgo Biloba
Ginseng
Glaucoma
Glucosamine
Goji
Golden Seal
Green Tea
Hair
Hay Fever
Headaches
IBD
IBS
Immune Support
Indian Ginseng
Inflammation
Insomnia
Iron
Joint Relief
Korean Ginseng
Laxative
Liver Detox & Support
Longevity
Lower Back Pain
Lung Health
Leutin
Lycopene
Macular Health
Male Potency
Male Stamina
Mangosteen
Melatonin
Memory
Menopause
Men’s Health
Menstruation
Mercury Detox
Migraines
Milk Thistle
Minerals --Research

Mood & Behavior

MSM
Nails
Niacin
Noni
Omega 3
Osteoporosis
Parkinson’s Disease
Periodontal Health
PMS
Pomegranate
Pregnancy
Pregnenolone
Progesterone Therapy
Prostate Health
Quercetin-Bromelain
Rheumatism
SAMe
Selenium
Senior Citizens

Senior Daily Formula
Serotonin Activator
Sexual Performance

Shark Cartilage
Sickle Cell
Sinusitis
Skin Disorders
Skin Health
Sleep Problems
Smokers
Sports Performance
St John's Wort
Stomach Problems
Stress Relief
Stroke
Tanning
Taurine
Thyroid Health
Tumors
Ulcers
Universal Vitamin
Valerian Root
Vegetarians
Vision
Vitality
Vitamin Research
Vitamin B-6
Vitamin B-12
Vitamin B Complex
Vitamin C
Vitamin D
Vitamin E
Wasabi
Weight Management
Women’s Health
Wound Healing

Zinc

Green Tea Extract

One of Nature’s Most Potent Nutrients
for Proper Body Functioning

1 Capsule = 5 Cups

 

   Formula 101.            60 Capsules.   1-2 Daily.

   Green Tea Leaf Extract 500mg per capsule
   Price Range: 1-2 Containers:   $11.95 each.   3-5:  $10.95.    6+: $9.95

SPECIAL OFFER!

RECEIVE A FREE PRODUCT
WITH EACH ORDER

(We will send you a free product every time you place an order.)

Have a Healthy & Prosperous Year!



 

Quality Assurance: This product is manufactured in the United States and is produced from natural sources and contains no yeast, sugar, starch, artificial flavor, dyes, coloring agent or preservatives.  


 

Green Tea Extract contains powerful antioxidants which promote overall good health, strengthen the immune system, support cognitive function, and reduce the risk of diseases. See a partial listing of uses, as cited by the University of Maryland.

The active ingredients of green tea are called polyphenols and have been researched as part of treatments for a remarkably wide variety of diseases, such as cancer, heart disease, hypertension, diabetes, and liver disease.

 

Researchers have proven that green tea may prevent coronary heart disease by promoting the health of cells that make up the artery wall (Phytother-Res.)

Additionally, researchers have found that green tea, coupled with a low-saturated diet, significantly lowers total cholesterol and raises good cholesterol (Archives of Internal Medicine). 

“Epigallo-catechin gallate (EGCG) is the major Polyphenol found in Green Tea. EGCG has anti-tumor-promoting effect.”
---Journal of Biological Chemistry. 2005 Apr. 29, v. 280, no. 17 p. 16882-16890


GREEN TEA AND CANCER:

According to the Journal of the National Cancer Institute, green tea has been proven to reduce the risk of cancer or even reverse its effects.  Polyphenols, the powerful antioxidants present in green tea in high concentrations, help kill cancerous cells and stop the progression of many types of the disease, including bladder cancer, breast cancer, colon cancer, and especially skin cancer.  Green tea protects the skin by blocking harmful UV rays and prolonging the life of skin cells (See: Curr-Drug-Targets-Immune-Endocr-Metabol-Discord).

 

SEE MEDICAL JOURNAL CITATIONS FOR GREEN TEA


GREEN TEA EXTRACT           

 

 

Serving Size: One capsule         Servings Per Container: 60



GREEN TEA EXTRACT: 500mg

Standardized to supply:
Epigallocatechin (EGCG) (30%)    150mg 
Other Polyphenol Catechins (65%)  325mg 
Naturally Occurring Caffeine 35mg

Quality Assurance: This product is produced from natural sources and contains no yeast, sugar, starch, artificial flavor or preservatives.

Recommended Dosage:
Take 1-2 capsules in the morning and/or afternoon.

 
Caution: Pregnant & breast-feeding women should avoid this product. People with heart problems, kidney disorders, stomach ulcers, and anxiety should not take green tea unless they have consulted with their physician.
See interactions
.  

 





The University of Maryland Medical Center
summarizes the uses of Green tea:


ATHEROSCLEROSIS
Population-based studies indicate that the antioxidant properties of green tea may help prevent atherosclerosis, particularly coronary artery disease. (Population-based studies refers to 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.)

HIGH CHOLESTEROL
Green tea has demonstrated an ability to lower total cholesterol and raise 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 thank 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.

CANCER
The cancer-protective effects of green tea have been reported in several population-based studies. For example, cancer rates tend to be low in countries such as Japan where green tea is regularly consumed. However, it is not possible to determine from these population-based studies whether green tea actually prevents cancer in people. Emerging animal and clinical studies are beginning to suggest that substances in green tea known as polyphenols may play an important role in the prevention of cancer. These substances act as powerful antioxidants. Researchers also believe that polyphenols help kill cancerous cells and stop its 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 with 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.

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 green tea can be recommended 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, results of studies in people have been conflicting. 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 findings, further research is needed before green tea can be recommended 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 esopageal cancers, further studies are needed before any conclusions can be drawn about green tea and lung cancer.

PANCREATIC CANCER
In one large-scale study comparing green tea drinkers with non-drinkers, 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. It is not clear from this population-based study, however, whether green tea is solely responsible for reducing pancreatic cancer risk. Although promising, further studies in animals and people are needed before green tea can be recommended 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. However, both green and black tea extracts were also found to stimulate genes that cause cells to be less sensitive to chemotherapy drugs. Given this potential interaction, black and green tea (as well as extracts of these teas) should not be taken 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 recent 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. Also, 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. More research in
this area would be helpful.

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 appears 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 at this time, 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, but there have been no specific studies of this herb in overweight or obese individuals. Some researchers speculate that substances in green tea known as polyphenols, specifically the catechins, are responsible for the herb's fat-burning effect.


BACKGROUND:

Green tea has been used as a medicinal supplement for thousands of years.  Ancient cultures in India and China were the first to recognize that green tea maintains cardiac health, regulates blood sugar, promotes a healthy metabolism, and improves mental processes (University of Maryland Medical Center).  Western countries have only more recently discovered this remarkable substance, and researchers all over the world are beginning to identify the specific properties of green tea which make it such a powerful dietary supplement.

“
Blueberries, pomegranates, green tea, and cabernet wine were among many antioxidant-rich foods and drinks shown to prevent disease in 1999. Antioxidants prevent the damage done to cells by free radicals, molecules that are released during the normal metabolic process of oxidation. Oxidation can lead to cancerous changes, accelerate the aging process, and contribute to heart disease and degenerative diseases such as arthritis.”

-----Encyclopedia Britannica


WHAT ARE GREEN TEA POLYPHENOLS?

The secret to green tea’s extraordinary health benefits lies in its naturally high concentration of polyphenols, chemicals present in other substances such as black tea, red wine, pomegranates, and a large number of other natural foods, all of which have been traditionally used in alternative medicine (Journal of Biological Chemistry).  Polyphenols act as antioxidants, preventing the harmful effects of oxidation on cells and tissue in the body.  Antioxidants have become increasingly popular today because of the increased presence of oxidation in our environment caused by ultraviolet light, radiation, cigarette smoke, and pollution (University of Maryland Medical Center).  Now more than ever the body needs the strength of antioxidants, and green tea contains antioxidants in higher concentration than almost any other naturally occurring food.


OTHER USES FOR GREEN TEA:

Green tea possesses several other medicinal properties.  In smokers, green tea has been shown to neutralize the carcinogenic properties of tobacco, as well as reduce the risk of oral cancers (Phytomedicine). 

As a great promoter of the health of cells, green tea can act as an anti-aging substance, prolonging the life of cells and preventing degeneration.  De-generation in neural tissue cells is a leading cause in diseases such as Alzheimer’s, and researchers have experimented with green tea extracts on Alzheimer’s patients to prove that green tea can be used to fight or even prevent the disease in persons of advanced age (Journal of Nutritional Biochemistry).

In addition to its role in cancer prevention and cellular health, green tea promotes a healthy metabolism and reduces the effects of stress on the body (Toxicol.Lett.).  As a dietary supplement, green tea has been used for weight management (British Journal of Nutrition).  Stress produces a larger amount of oxidation in the body, and the powerful antioxidants in green tea help to reduce oxidation from all sources.

Research into the specific causes of the benefits of green tea is ongoing.  By isolating the chemicals present in green tea which are the source of its healing, scientists are developing the best ways for delivering green tea’s health benefits.  Dietary supplements are a means of providing the antioxidants of green tea in high concentration, and are a natural and healthy means of promoting good cellular health (Mutat.-Res.).


           
CITATIONS:

“This preliminary work suggests that green tea extracts may play a role in weight management through increased energy expenditure.”
---- British Journal of Nutrition 2005 94:432-436.

“Green tea extract has a high polyphenol content…Significantly promotes cell survival….”
---- Life-Sci. 2005 Jun 3; 77(3): 345-58


“Green tea polyphenols were also found to inhibit the urinary mutagenicity [inducing mutations] in rats induced by tobacco extract. Moreover green tea polyphenols were found to inhibit in vitro nitrosation reaction produced by reaction sodium nitrite and methyl urea and further inhibition of mutagenicity indicating that green tea has dual action to bring out a reduction in the mutagenic and carcinogenic potential of tobacco.”
---- Phytomedicine. 2005 Mar; 12(3): 216-20


“Studies in cell culture and laboratory animals have shown that green tea and its major component, epigallocatechin-3-gallate, inhibit cell growth and reduce tumor incidence. The study, although preliminary, indicates that drinking green tea reduced the number of damaged cells in smokers by inducing cell growth arrest and apoptosis, a mechanism similar to that observed in cultured cells and animals. These results warrant a large-scale intervention trial to further verify the role of green tea in the prevention of oral cancer in smokers.”
----- Mol-Nutr-Food-Res. 2005 Jan; 49(1): 43-51


“Green tea extract (Sunphenon), which is rich in catechins (polyphenols)…”
---- J-Agric-Food-Chem. 2005 Jan 26; 53(2): 332-7


“Since green tea is considered to exert a number of beneficial health effects, green tea products are widely used as dietary supplements…”
---- Food Chemistry Toxicology. 2005 Feb; 43(2): 307-14


The potential protective roles played by green tea polyphenol (GTP) against the injurious effects of reactive oxygen species in human microvascular endothelial cells (HUMVECs) were investigated. These results demonstrate that GTP can act as a biological antioxidant in a cell culture experimental model and prevent oxidative stress-induced cytotoxicity [harmful to cells] in ECs.
---- Toxicol-Lett. 2005 Feb 15; 155(2): 269-75



Tea and tea constituents have been shown by different investigators to inhibit lung tumorigenesis in different animal model systems. In the tea-treated group, and in some experiments, decreased tumor incidence has also been observed. The green tea constituent, epigallocatechin-3-gallate (EGCG), and the black tea constituent, theaflavins, have also been shown to be effective.
---- Exp-Lung-Res. 2005 Jan-Feb; 31(1): 135-44



A naturally occurring gallated polyphenol isolated from green tea leaves, (-)-epigallocatechin gallate (EGCG), has been shown to be an inhibitor of dihydrofolate reductase (DHFR) activity in vitro at concentrations found in the serum and tissues of green tea drinkers (0.1-1.0 micromol/L). These data provide the first evidence that the prophylactic effect of green tea drinking on certain forms of cancer, suggested by epidemiologic studies, is due to the inhibition of DHFR by EGCG and could also explain why tea extracts have been traditionally used in "alternative medicine" as anti-carcinogenic/antibiotic agents or in the treatment of conditions such as psoriasis.
---- Cancer-Research. 2005 Mar 15; 65(6): 2059-64



Tea consumption is varying its status from a mere ancient beverage and a lifestyle habit, to a nutrient endowed with possible prospective neurobiological-pharmacological actions beneficial to human health. Accumulating evidence suggest that oxidative stress resulting in reactive oxygen species generation and inflammation play a pivotal role in neurodegenerative diseases, supporting the implementation of radical scavengers, transition metal (e.g., iron and copper) chelators, and nonvitamin natural antioxidant polyphenols in the clinic. These observations are in line with the current view that polyphenolic dietary supplementation may have an impact on cognitive deficits in individuals of advanced age. As a consequence, green tea polyphenols are now being considered as therapeutic agents in well controlled epidemiological studies, aimed to alter brain aging processes and to serve as possible neuro-protective agents in progressive neurodegenerative disorders such as Parkinson's and Alzheimer's diseases
--- Journal of Nutritional Biochemistry. 2004 Sept., v. 15, no. 9 p. 506-516



Among the promising bioactive food components being investigated at the National Cancer Institute in prevention clinical trials to reduce breast cancer risk are indole-3-carbinol, sulforaphanes, phytoestrogen isoflavones, perillyl alcohol, and green tea polyphenols…. selenium and vitamin E. Soy isoflavones, green tea polyphenols, and doxercalciferol also are being investigated for prostate cancer prevention.
---- J-Nutr. 2004 Dec; 134(12 Suppl): 3507S-3512S


The results presented herein are consistent with EGCG [Green Tea component] acting as a pro-oxidant, with the cancerous cells more sensitive to oxidative stress than the normal cells.
---- Basic-Clin-Pharmacol-Toxicol. 2004 Oct; 95(4): 191-200


It has been reported that tea extracts have antibacterial, antiviral, antioxidative, antitumor and antimutagenic activities. The protective effect of green tea has been assumed to be due to the powerful scavenging and antioxidative property of high concentrations of unpolymerised catechins and their gallates…possesses excellent DPPH free radical scavenging activity.
---- Mutat-Res. 2004 Nov 22; 556(1-2): 65-74


The primary target of licensed drugs for the treatment of Alzheimer's disease is the inhibition of the enzyme acetylcholinesterase, although preventing beta-amyloidosis is a prime target for drugs in development. The in vitro dual anti-cholinesterase and beta-secretase activities of Camellia sinensis L. extract (tea) is reported. Green and black tea inhibited human acetylcholinesterase (AChE) with IC(50) values of 0.03 mg/mL and 0.06 mg/mL respectively, and human butyrylcholinesterase (BuChE) with IC(50) values 0.05 mg/mL. Green tea at a final assay concentration of 0.03 mg/mL inhibited beta-secretase by 38%. These novel findings suggest that tea infusions contain biologically active principles, perhaps acting synergistically, that may be used to retard the progression of the disease assuming that these principles, yet to be identified, reach the brain. Copyright (c) 2004 John Wiley & Sons, Ltd.
---- Phytother-Res. 2004 Aug; 18(8): 624-7


We show that administration of green tea that contains EGCG caused a reduction in the level of mRNAs for gluconeogenic enzymes, phosphoenolpyruvate carboxykinase and glucose-6-phosphatase in the mouse liver. EGCG alone was also found to down-regulate the gene expression of these enzymes but not so curcumin or quercetin. The results of this study support the idea that green tea intake may be beneficial in the prevention of diabetes mellitus.
----- Planta-Med. 2004 Nov; 70(11): 1100-2


In cancer, a high flux of oxidants not only depletes the cellular thiols, but damages the whole cell as well. Epidemiological studies suggest green tea may mitigate cancers in human and animal models for which several mechanisms have been proposed.
---- Chem-Biol-Interact. 2004 Oct 15; 149(2-3): 81-7


OBJECTIVE: To determine the impact of nutritional supplementation on optimization of reproductive health in women… a proprietary nutritional supplement containing chasteberry and green tea extracts, L-arginine, vitamins (including folate) and minerals… Nutritional supplementation may provide an attractive alternative or complement to conventional fertility therapy.
---- J-Reprod-Med. 2004 Apr; 49(4): 289-93


The genomics of atherosclerosis can arise as a result of cross-talk between the genes coding for the LDL-receptor (LDL-R), LXR-alpha, PPARs (alpha, gamma), CD36 and C-myc because these genes control lipid metabolism, cytokine production and cellular activity within the arterial wall. The effect of green tea polyphenols (GTPs) upon such genomics revealed their ability to down-regulate genes coding for PPAR-gamma, CD36, LXR-alpha, C-myc coupled with up-regulation of genes coding for LDL-R and PPAR-alpha at the transcriptional level. Based upon these results, it is proposed that GTPs have the inherent capacity to inhibit the development of atherosclerotic lesions. Copyright 2004 John Wiley & Sons, Ltd.
---- Phytother-Res. 2004 Feb; 18(2): 177-9


Green tea is widely consumed in Asian countries and is becoming increasingly popular in Western countries. Epidemiologically, it has been suggested that green tea consumption prevents type 2 diabetes…. Green tea promoted glucose metabolism in healthy human volunteers at 1.5 g/body in oral glucose tolerance tests. Green tea also lowered blood glucose levels… The present study provides evidence that green tea has an anti-diabetic effect.
---- BMC-Pharmacol. 2004 Aug 26; 4(1): 18


Green tea may prevent cancer, partially by inhibiting tumor angiogenesis. Our previous studies showed that green tea extract was effective in inhibiting breast cancer and endothelial cell proliferation in vitro, and suppressed xenograft size and decreased the tumor vessel density in vivo….This study contributes to the comprehensive analysis of the molecular effects of green tea on endothelial cells, and provides insight into genes that may be important in chemoprevention.
----- International Journal of Oncology. 2004 Jul; 25(1): 193-202


Alveolar bone resorption is a characteristic feature of periodontal diseases and involves the removal of both the mineral and organic constituents of the bone matrix …These findings suggest that EGCG may prevent the alveolar bone resorption that occurs in periodontal diseases by inhibiting the expression of MMP-9 in osteoblasts and the formation of osteoclasts
--- Journal of Periodontal Research. 2004 Oct; 39(5): 300-7

Recently, considerable attention has been focused on dietary and medicinal phytochemicals that inhibit, reverse, or retard diseases caused by oxidative and inflammatory processes. Green tea polyphenols have both antioxidant and anti-inflammatory properties…. Green tea polyphenols reduce the severity of liver injury in association with lower concentrations of lipid peroxidation and pro-nflammatory nitric oxide-generated mediators. Green tea polyphenols can be a useful supplement in the treatment of liver disease and should be considered for liver conditions in which pro-inflammatory and oxidant stress responses are dominant.
--- Am-J-Clin-Nutr. 2004 Sep; 80(3): 742-51

Catechins and theaflavins, polyphenolic compounds derived from tea (Camellia sinensis, fam. Theaceae), have been reported to have a wide range of biological activities including prevention of tooth decay and oral cancer. The present study was undertaken to determine the usefulness of green tea leaves and black tea extract for the delivery of catechins and theaflavins to the oral cavity…. These results indicate that tea leaves can be used as a convenient, slow-release source of catechins and theaflavins and provide information for the possible use of tea in the prevention of oral cancer and dental caries.
---- Cancer-Epidemiol-Biomarkers-Prev. 2004 Jan; 13(1): 132-7

Green tea extract exhibited significantly lower total cholesterol, LDL cholesterol and total cholesterol to HDL cholesterol ratios compared with baseline… Tea consumption has been associated with decreased cardiovascular risk… The theaflavin-enriched green tea extract we studied is an effective adjunct to a low-saturated-fat diet to reduce LDL-C in hypercholesterolemic adults and is well tolerated.
--- Archives of Internal Medicine. 2003 Jun 23; 163(12): 1448-53

Green tea has been shown to help prevent cancer in animal studies…(EGCG) is believed to be an important active ingredient in green tea responsible for this chemo-preventive activity… Several human cancer cells (esophageal squamous, colon, and prostate) were exposed to varying doses of EGCG. The results of this study show that EGCG inhibits DNA methyltransferase activity and causes CpG demethylation and reactivation of methylation-silenced genes.
--- Journal of the National Cancer Institute 2003 95: 1477-1481.

 

(FOR MORE STUDIES ON GREEN TEA)


Possible Interactions with Green Tea:

Also listed as: Camellia sinensis
 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 healthcare provider:

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.

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
Green tea should not be taken with warfarin, a blood-thinning medication, because the herb contains vitamin K and, thus, can render warfarin ineffective.

Similarly, green tea and aspirin should not be mixed because they both prevent platelets from clotting. Using the two together, therefore, may increase your risk of bleeding.

CHEMOTHERAPY
The combination of green tea and chemotherapy medications, specifically doxorubicin and tamoxifen, increased the effectiveness of these medications in laboratory tests. These results have not yet been demonstrated in studies of people, however.

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, black and green tea (as well as extracts of these teas) should not be taken 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.


ADDITIONAL STUDIES ON GREEN TEA:

Epigallocatechin-3-gallate (EGCG): Chemical and biomedical perspectives.
Author: Nagle,-DG; Ferreira,-D; Zhou,-YD
Citation: Phytochemistry-. 2006 Sept; 67(17): 1849-1855.

Abstract: The compound (-)epigallocatechin3gallate (EGCG) is the major catechin found in green tea [Camellia sinensis L. Ktze. (Theaceae)]. This polyphenolic compound and several related catechins are believed to be responsible for the health benefits associated with the consumption of green tea. The potential health benefits ascribed to green tea and EGCG include antioxidant effects, cancer chemoprevention, improving cardiovascular health, enhancing weight loss, protecting the skin from the damage caused by ionizing radiation, and others. The compound EGCG has been shown to regulate dozens of diseasespecific molecular targets. Many of these molecular targets are only affected by concentrations of EGCG that are far above the levels achieved by either drinking green tea or consuming moderate doses of green tea extractbased dietary supplements. In spite of this, welldesigned doubleblinded controlled clinical studies have recently demonstrated the efficacy of green tea extracts and purified EGCG products in patients. Therefore, this review highlights results from what the authors believe to be some of the most clinically significant recent studies and describes current developments in the stereoselective total synthesis of EGCG.


Green tea extract and its major polyphenol (-)-epigallocatechin gallate improve muscle function in a mouse model for Duchenne muscular dystrophy.
Author: Dorchies,-O-M; Wagner,-S; Vuadens,-O; Waldhauser,-K; Buetler,-T-M; Kucera,-P; Ruegg,-U-T
Citation: Am-J-Physiol-Cell-Physiol. 2006 Feb; 290(2): C616-25

Abstract: Duchenne muscular dystrophy is a frequent muscular disorder caused by mutations in the gene encoding dystrophin, a cytoskeletal protein that contributes to the stabilization of muscle fiber membrane during muscle activity. Affected individuals show progressive muscle wasting that generally causes death by age 30. In this study, the dystrophic mdx(5Cv) mouse model was used to investigate the effects of green tea extract, its major component (-)-epigallocatechin gallate, and pentoxifylline on dystrophic muscle quality and function. Three-week-old mdx(5Cv) mice were fed for either 1 or 5 wk a control chow or a chow containing the test substances. Histological examination showed a delay in necrosis of the extensor digitorum longus muscle in treated mice. Mechanical properties of triceps surae muscles were recorded while the mice were under deep anesthesia. Phasic and tetanic tensions of treated mice were increased, reaching values close to those of normal mice. The phasic-to-tetanic tension ratio was corrected. Finally, muscles from treated mice exhibited 30-50% more residual force in a fatigue assay. These results demonstrate that diet supplementation of dystrophic mdx(5Cv) mice with green tea extract or (-)-epigallocatechin gallate protected muscle against the first massive wave of necrosis and stimulated muscle adaptation toward a stronger and more resistant phenotype.


Green tea (Camellia sinensis) extract ameliorates endotoxin induced sickness behavior and liver damage in rats.
Author: Singal,-A; Tirkey,-N; Pilkhwal,-S; Chopra,-K
Citation: Phytother-Res. 2006 Feb; 20(2): 125-9

Abstract: Immune activation, either by cytokines or endotoxin, elicits a constellation of nonspecific symptoms such as weakness, malaise, listlessness, fatigue, adipsia, anorexia, depression and anxiety collectively termed as sickness behavior. Further, endotoxin administration in animals has been implicated in the pathogenesis of many types of liver disease. Green tea, a common household drink, is rich in antioxidant polyphenols demonstrating inhibitory effects on cytokine production. The present study was designed to investigate the effect of chronic treatment of green tea extract (GTE) on lipopolysaccharide (LPS)-induced sickness behavior and liver damage in rats. The hypothesis was tested through the analysis of LPS-induced behavioral changes in rats, in plus maze and open field paradigms. Other parameters such as feeding and water consumption, weight loss and organ weight index were also estimated. Liver function tests were conducted to investigate the effect of GTE supplementation on LPS-induced hepatic dysfunction. The results of the study demonstrated that GTE significantly attenuated LPS-induced sickness behavior as well as hepatic damage either by its antioxidant activity or by inhibiting LPS induced cytokine production in rats. Copyright 2006 John Wiley & Sons, Ltd


Intracellular signaling network as a prime chemopreventive target of (-)-epigallocatechin gallate. Author: Na,-H-K; Surh,-Y-J

Citation: Mol-Nutr-Food-Res. 2006 Feb; 50(2): 152-9 Abstract: Chemoprevention is an attempt to use either naturally occurring or synthetic substances or their mixtures to intervene in the progress of carcinogenesis. Recently, it has been shown that some edible phytochemicals alter gene expression, directly or indirectly, thereby regulating the carcinogenic processes. (-)-Epigallocatechin gallate (EGCG), a principal antioxidant derived from green tea, is one of the most extensively investigated chemopreventive phytochemicals. EGCG has been known to block each stage of carcinogenesis by modulating signal transduction pathways involved in cell proliferation, transformation, inflammation, apoptosis, metastasis and invasion. This review addresses the molecular target-based chemoprevention with EGCG by focusing on the common events mediated by transcription factors, such as NF-kappa B, activator protein-1 and nuclear factor erythroid 2 p45-related factor, and upstream kinases involved in the cellular signaling network.


Matrix metalloproteinases in cancer metastasis: molecular targets for prostate cancer prevention by green tea polyphenols and grape seed proanthocyanidins.
 Author: Katiyar,-S-K
Citation: Endocr-Metab-Immune-Disord-Drug-Targets. 2006 Mar; 6(1): 17-24

Abstract: Matrix metalloproteinases (MMP) play a crucial role in the development and metastatic spread of cancer. One of the earliest events in the metastatic spread of cancer is the invasion through the basement membrane and proteolytic degradation of the extracellular matrix proteins, such as, collagens, laminin, elastin and fibronectin etc, and non-matrix proteins. MMPs are the important regulators of tumor growth, both at the primary site and in distant metastases. Given the clear implications of MMPs in many human cancers, MMPs remain important targets of cancer therapy. Metastatic spread of cancer continues to be the greatest barrier in prevention or cure of cancer. The recognition that MMPs facilitate tumor cell growth, invasion and metastasis of cancer has led to the development of MMP inhibitors as cancer therapeutic agents. Understanding the molecular mechanism of metastasis is also crucial for the design and effective use of novel therapeutic strategies to combat metastases. In this short review article, we discuss the evidences that MMPs are associated with cancer metastasis and that they make a functional contribution to the process. Further, since considerable interest among human population is increasing with regard to the use of dietary botanical supplements for the prevention of age-associated diseases like some forms of cancer, we also discuss the beneficial effects of dietary botanicals, such as green tea polyphenols and grape seed proanthocyanidins, in chemoprevention of cancer with particular emphasis on the involvement of MMPs in prostate cancer.




Inhibition of CWR22Rnu1 tumor growth and PSA secretion in athymic nude mice by green and black teas.
Author: Siddiqui,-I-A; Zaman,-N; Aziz,-M-H; Reagan-Shaw,-S-R; Sarfaraz,-S; Adhami,-V-M; Ahmad,-N; Raisuddin,-S; Mukhtar,-H
Citation: Carcinogenesis. 2006 Apr; 27(4): 833-9 Abstract: Cancer of the prostate gland (CaP), the most common invasive malignancy and a major cause of cancer related deaths in male population in the USA, is an ideal candidate disease for chemoprevention because it is typically detected in elderly population with a relatively slower rate of growth and progression. Many dietary phytochemicals are showing promising chemopreventive effects, at-least in pre-clinical models of CaP. Our published data in cell culture and animal studies, supported by the work from other laboratories, as well as epidemiological observations and case-control studies, suggest that polyphenols present in green tea possess CaP chemopreventive and possibly therapeutic effects. This present study was designed to compare CaP cancer chemopreventive effects of green tea polyphenols (GTP), water extract of black tea, and their major constituents epigallocatechin-3-gallate and theaflavins, respectively, in athymic nude mice implanted with androgen-sensitive human CaP CWR22Rnu1 cells. Our data demonstrated that the treatment with all the tea ingredients resulted in (i) significant inhibition in growth of implanted prostate tumors, (ii) reduction in the level of serum prostate specific antigen, (iii) induction of apoptosis accompanied with upregulation in Bax and decrease in Bcl-2 proteins, and (iv) decrease in the levels of VEGF protein. Furthermore, we also found that GTP (0.01 or 0.05% w/v; given after establishment of CWR22Rnu1 tumor) causes a significant regression of tumors suggesting therapeutic effects of GTP at human achievable concentrations.


Chemoprevention of photocarcinogenesis by selected dietary botanicals.
Author: Baliga,-M-S; Katiyar,-S-K
Citation: Photochem-Photobiol-Sci. 2006 Feb; 5(2): 243-53

Abstract: Epidemiological, clinical and laboratory studies have implicated solar ultraviolet (UV) radiation as a tumor initiator, tumor promoter and complete carcinogen, and their excessive exposure can lead to the development of various skin disorders including melanoma and nonmelanoma skin cancers. Sunscreens are useful, but their protection is not adequate to prevent the risk of UV-induced skin cancer. It may be because of inadequate use, incomplete spectral protection and toxicity. Therefore new chemopreventive methods are necessary to protect the skin from photodamaging effects of solar UV radiation. Chemoprevention refers to the use of agents that can inhibit, reverse or retard the process of skin carcinogenesis. In recent years, considerable interest has been focused on identifying naturally occurring botanicals, specifically dietary, for the prevention of photocarcinogenesis. A wide variety of botanicals, mostly dietary flavonoids or phenolic substances, have been reported to possess substantial anticarcinogenic and antimutagenic activities because of their antioxidant and antiinflammatory properties. This review summarizes chemopreventive effects of some selected botanicals, such as apigenin, curcumin, grape seed proanthocyanidins, resveratrol, silymarin, and green tea polyphenols, against photocarcinogenesis in in vitro and in vivo systems. Attention has also been focused on highlighting the mechanism of chemopreventive action of these dietary botanicals. We suggest that in addition to the use of these botanicals as dietary supplements for the protection of photocarcinogenesis, these botanicals may favorably supplement sunscreens protection and may provide additional antiphotocarcinogenic protection including the protection against other skin disorders caused by solar UV radiation.

 

 


Catechin-vanilloid synergies with potential clinical applications in cancer.
Author: Morre,-D-M; Morre,-D-J
Citation: Rejuvenation-Res. 2006 Spring; 9(1): 45-55

Abstract: A cancer-specific cell surface protein, tNOX, has been identified as a target for low-dose cell killing (apoptosis) of cancer cells by green tea catechins and Capsicum vanilloid combinations. This protein is uniquely associated with all forms of cancer and is absent from normal cells and tissues. Its activity is correlated with cancer growth. When blocked, cancer cells fail to enlarge after division and eventually die. Among the most potent and effective inhibitors of tNOX are naturally occurring polyphenols exemplified by the principal green tea catechin (-)-epigallocatechin gallate (EGCg) and the vanilloid capsaicin. Catechin-vanilloid combinations are 10 to 100 times more effective than either catechins or vanilloids alone. Vector-forced overexpression of tNOX cDNA and antisense has demonstrated that the tNOX target is both necessary and sufficient to explain the anticancer properties of green tea catechins alone and in vanilloid-containing combinations. The necessity and sufficiency of tNOX was validated as the catechin target with transgenic mice overexpressing the processed form of tNOX. Transgenic mice grew faster and the increased growth caused by tNOX overexpression was blocked by EGCg in the drinking water. A catechin-vanilloid mixture where one 350-mg capsule is equivalent to 16 cups of green tea in its ability to inhibit tNOX and growth of cancer cells in culture is undergoing clinical evaluation as a therapeutic aid for cancer patients.



Natural products and the treatment of leukemia.

Author: Hamblin,-T Citation: Leuk-Res. 2006 Jun; 30(6): 649-50

Abstract: Plants have been the source of many medicines in the pharmacopoeia. So much so that an industry has arisen selling plant extracts as health foods. To a great degree it operates over the internet and it chiefly caters to the worried well. However, cancer patients frequently take plant extracts in addition to their prescribed medicines. These extracts are not biologically inactive, and many have important pro-apoptotic effects on cancer cell-lines in vitro. In this issue a study of the in vivo effects of green tea extract in low grade lymphomas is reported. The results are sufficiently encouraging to initiate a formal clinical trial.



Clinical effects of oral green tea extracts in four patients with low grade B-cell malignancies.
Author: Shanafelt,-T-D; Lee,-Y-K; Call,-T-G; Nowakowski,-G-S; Dingli,-D; Zent,-C-S; Kay,-N-E Citation: Leuk-Res. 2006 Jun; 30(6): 707-12

Abstract: Green tea or its constituents have long been touted as a health promoting substance including claims it may have cancer prevention properties. We previously reported the in vitro ability of one tea polyphenol, epigallocatechin gallate (EGCG), to induce apoptotic cell death in the leukemic B-cells from a majority of patients with chronic lymphocytic leukemia (CLL). After the publication of our findings many patients with CLL and other low grade lymphomas began using over-the-counter products containing tea polyphenols despite the absence of evidence to suggest clinical benefit, definition of possible toxicities, or information on optimal dose and schedule. We have become aware of four patients with low grade B-cell malignancies seen in our clinical practice at Mayo Clinic who began, on their own initiative, oral ingestion of EGCG containing products and subsequently appeared to have an objective clinical response. Three of these four patients met criteria for partial response (PR) by standard response criteria. Although spontaneous remission/regression is occasionally observed in individuals with low grade B-cell malignancies, such events are rare. Several patients presented here had documented steady clinical, laboratory, and/or radiographic evidence of progression immediately prior to initiation of over-the-counter green tea products and then developed objective responses shortly after self-initiating this therapy. Such anecdotes highlight the need for clinical trials of tea polyphenols to define the optimal dosing, schedule, toxicities, and clinical efficacy before widespread use can be recommended. An NCI sponsored phase I/II trial of de-caffeinated green tea extracts for patients with asymptomatic, early stage CLL opened at Mayo Clinic in August 2005.



Suppression of Wnt signaling by the green tea compound (-)-epigallocatechin 3-gallate (EGCG) in invasive breast cancer cells. Requirement of the transcriptional repressor HBP1.
Author: Kim,-J; Zhang,-X; Rieger-Christ,-K-M; Summerhayes,-I-C; Wazer,-D-E; Paulson,-K-E; Yee,-A-S
Citation: J-Biol-Chem. 2006 Apr 21; 281(16): 10865-75

Abstract: Genetic and biochemical de-regulation of Wnt signaling is correlated with breast and other cancers. Our goal was to identify compounds that block Wnt signaling as a first step toward investigating new strategies for suppression of invasive and other breast cancers. In a limited phytonutrient screen, EGCG ((-)-epigallocatechin 3-gallate), the major phytochemical in green tea, emerged as an intriguing candidate. Epidemiological studies have associated green tea consumption with reduced recurrence of invasive and other breast cancers. Wnt signaling was inhibited by EGCG in a dose-dependent manner in breast cancer cells. The apparent mechanism targeted the HBP1 transcriptional repressor, which we had previously characterized as a suppressor of Wnt signaling. EGCG treatment induced HBP1 transcriptional repressor levels through an increase in HBP1 mRNA stability, but not transcriptional initiation. To test functionality, DNA-based short hairpin RNA (shRNA) was used to knockdown the endogenous HBP1 gene. Consistently, the HBP1 knockdown lines had reduced sensitivity to EGCG in the suppression of Wnt signaling and of a target gene (c-MYC). Because our ongoing studies clinically link abrogation of HBP1 with invasive breast cancer, we tested if EGCG also regulated biological functions associated with de-regulated Wnt signaling and with invasive breast cancer. EGCG reduced both breast cancer cell tumorigenic proliferation and invasiveness in an HBP1-dependent manner. Together, the emerging mechanism is that EGCG blocks Wnt signaling by inducing the HBP1 transcriptional repressor and inhibits aspects of invasive breast cancer. These studies provide a framework for considering future studies in breast cancer treatment and prevention.



A new approach to managing oral manifestations of Sjogren's syndrome and skin manifestations of lupus.
Author: Hsu,-S; Dickinson,-D
Citation: J-Biochem-Mol-Biol. 2006 May 31; 39(3): 229-39

Abstract: Sjogren's syndrome (SS) is an autoimmune disorder that affects the salivary glands, leading to xerostomia, and the lacrimal glands, resulting in xerophthalmia. Secondary SS is associated with other autoimmune disorders such as systemic rheumatic diseases and systemic lupus erythematosis (SLE), which can affect multiple organs, including the epidermis. Recent studies have demonstrated that green tea polyphenols (GTPs) possess both anti-inflammatory and anti-apoptotic properties in normal human cells. Epidemiological evidence has indicated that, in comparison to the United States, the incidence of SS, clinical xerostomia and lupus is considerably lower in China and Japan, the two leading green tea-consuming countries.Thus, GTPs might be responsible, in part, for geographical differences in the incidence of xerostomia by reducing the initiation or severity of SS and lupus. Consistent with this, molecular, cellular and animal studies indicate that GTPs could provide protective effects against autoimmune reactions in salivary glands and skin. Therefore, salivary tissues and epidermal keratinocytes could be primary targets for novel therapies using GTPs. This review article evaluates the currently available research data on GTPs, focusing on their potential application in the treatment of the oral manifestations of SS and skin manifestations of SLE.




Green tea polyphenol inhibits Mycobacterium tuberculosis survival within human macrophages.
Author: Anand,-P-K; Kaul,-D; Sharma,-M
Citation: Int-J-Biochem-Cell-Biol. 2006; 38(4): 600-9
Abstract: Lack of maturation of phagosomes containing pathogenic Mycobacterium tuberculosis within macrophages has been widely recognized as a crucial factor for the persistence of mycobacterial pathogen. Host molecule tryptophan-aspartate containing coat protein (TACO) has been shown to play a crucial role in the arrest of such a maturation process. The present study was addressed to understand whether or not polyphenols derived from green tea could down-regulate TACO gene transcription. And if yes, what impact TACO gene down-regulation has on the uptake/survival of M. tuberculosis within macrophages. The reverse-transcriptase polymerase chain reaction and reporter assay technology, employed in this study, revealed that the major component of green tea polyphenols, epigallocatechin-3-gallate had the inherent capacity to down-regulate TACO gene transcription within human macrophages through its ability to inhibit Sp1 transcription factor. We also found out that TACO gene promoter does contain Sp1 binding sequence using bioinformatics tools. The down-regulation of TACO gene expression by epigallocatechin-3-gallate was accompanied by inhibition of mycobacterium survival within macrophages as assessed through flow cytometry and colony counts. Based on these results, we propose that epigallocatechin-3-gallate may be of importance in the prevention of tuberculosis infection.




Polyphenols and gastrointestinal diseases.
Author: Dryden,-G-W; Song,-M; McClain,-C
Citation: Curr-Opin-Gastroenterol. 2006 Mar; 22(2): 165-70
Abstract: PURPOSE OF REVIEW: This article will review the role of polyphenols in gastrointestinal diseases. Ingested polyphenols are concentrated in the gastrointestinal tract and are not well absorbed into the rest of the body. Thus, the high luminal concentrations achieved support a potential for therapeutic uses in the gastrointestinal tract. Additionally, there is great interest from the general public in complementary and alternative medicine. RECENT FINDINGS: Dietary polyphenols are a major source of antioxidants consumed by humans. Polyphenols possess not only antioxidant properties but also antiviral, antibacterial, antiinflammatory and anticarcinogenic effects, as well as the ability to modulate certain signaling pathways such as nuclear factor-kappaB activation. Green tea polyphenols have been shown to have efficacy in various models of inflammatory bowel disease. Silymarin, or milk thistle, is hepatoprotective against many forms of experimental liver injury and is widely used in human liver diseases, such as hepatitis C and alcoholic cirrhosis, with an excellent safety profile (but with unclear efficacy). SUMMARY: Substantial in-vitro and animal studies support the beneficial effects of polyphenols in many gastrointestinal diseases. Well designed multicenter trials in humans, such as those called for in the 2005 National Institutes of Health Requests for Applications for Silymarin Centers, will be critical for defining the safety, appropriate dosing and therapeutic efficacy of such agents.




Green tea extract improves running endurance in mice by stimulating lipid utilization during exercise.
Author: Murase,-T; Haramizu,-S; Shimotoyodome,-A; Tokimitsu,-I; Hase,-T
Citation: Am-J-Physiol-Regul-Integr-Comp-Physiol. 2006 Jun; 290(6): R1550-6

Abstract: A series of polyphenols known as catechins are abundant in green tea, which is consumed mainly in Asian countries. The effects of catechin-rich green tea extract (GTE) on running endurance and energy metabolism during exercise in BALB/c mice were investigated. Mice were divided into four groups: nonexercise control, exercise control (Ex-cont), exercise+0.2% GTE, and exercise+0.5% GTE groups. Treadmill running time to exhaustion, plasma biochemical parameters, skeletal muscle glycogen content, beta-oxidation activity, and malonyl-CoA content immediately after exercise were measured at 8-10 wk after the initiation of the experiment. Oxygen consumption and respiratory exchange ratio were measured using indirect calorimetry. Running times to exhaustion in mice fed 0.5% GTE were 30% higher than in Ex-cont mice and were accompanied by a lower respiratory exchange ratio, higher muscle beta-oxidation activity, and lower malonyl-CoA content. In addition, muscle glycogen content was high in the GTE group compared with the Ex-cont group. Plasma lactate concentrations in mice fed GTE were significantly lower after exercise, concomitant with an increase in free fatty acid concentrations. Catechins, which are the main constituents of GTE, did not show significant effects on peroxisome proliferator-activated receptor-alpha or delta-dependent luciferase activities. These results suggest that the endurance-improving effects of GTE were mediated, at least partly, by increased metabolic capacity and utilization of fatty acid as a source of energy in skeletal muscle during exercise



Anticancer activity of grape and grape skin extracts alone and combined with green tea infusions.
Author: Morre,-D-M; Morre,-D-J Citation: Cancer-Lett. 2006 Jul 18; 238(2): 202-9
Abstract: Grapes and grape extracts were compared for inhibition of a growth-related and cancer-specific form of cell surface NADH oxidase with protein disulfide-thiol interchange activity designated tNOX from human cervical carcinoma (HeLa) cells and growth of HeLa and mouse mammary 4T1 cells in culture and transplanted tumors in mice. Grapes and grape extracts of several varieties had activity. With an extracted grape preparation provided by the California Table Grape Commission, an active fraction was eluted with methanol from a Diaion HP-20 column after removal of inactive water-soluble materials. Grape skins were a much more potent source than either grape pulp, juice or seeds. Ethanol extracts of the ground freeze-dried pomace was an excellent source. The grape extracts interacted, often synergistically, with decaffeinated green tea extracts both in the inhibition of tNOX activity and in the inhibition of cancer cell growth. Intratumoral injections of a 25:1 mixture of a green tea extract plus ground freeze-dried pomace was nearly as effective as standard synergistic green tea-Capsicum mixtures in inhibiting growth of 4T1 mammary tumors in situ in mice.



Green tea extract and (-)-epigallocatechin-3-gallate inhibit hypoxia- and serum-induced HIF-1alpha protein accumulation and VEGF expression in human cervical carcinoma and hepatoma cells.
Author: Zhang,-Q; Tang,-X; Lu,-Q; Zhang,-Z; Rao,-J; Le,-A-D
Citation: Mol-Cancer-Ther. 2006 May; 5(5): 1227-38

Abstract: Green tea extract and its major component (-)-epigallocatechin-3-gallate (EGCG) exhibit antiangiogenic activities in various experimental tumor models. A growing body of evidence has established that hypoxia-inducible factor-1alpha (HIF-1alpha) and its downstream target, vascular endothelial growth factor (VEGF), play a critical role in tumor angiogenesis. In this study, we investigated the effect of green tea extract and EGCG on HIF-1alpha and VEGF expression in human cervical carcinoma (HeLa) and hepatoma (HepG2) cells. Our results showed that green tea extract and EGCG significantly inhibited hypoxia- and serum-induced HIF-1alpha protein accumulation in these cancer cells but had no effects on HIF-1alpha mRNA expression. Suppression of HIF-1alpha protein by green tea extract and EGCG also resulted in a drastic decrease in VEGF expression at both mRNA and protein levels. The mechanisms of green tea extract and EGCG inhibition of hypoxia-induced HIF-1alpha protein accumulation seem to involve the blocking of both phosphatidylinositol 3-kinase/Akt and extracellular signal-regulated kinase 1/2 signaling pathways and the enhancing of HIF-1alpha protein degradation through the proteasome system. In addition, green tea extract and EGCG inhibited serum-induced HIF-1alpha protein and VEGF expression by interfering with the phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin signaling pathways, which play a crucial role in the protein translational machinery cascade. Functionally, green tea extract and EGCG abolished both chemoattractant- and hypoxia-stimulated HeLa cell migration. Our data suggested that HIF-1alpha/VEGF function as therapeutic target for green tea extract and EGCG in the context of cancer chemoprevention and anticancer therapy.



Inhibition of angiotensin converting enzyme activity by flavanol-rich foods.
Author: Actis-Goretta,-L.; Ottaviani,-J.I.; Fraga,-C.G.
Citation: Journal of agricultural and food chemistry. 2006 Jan. 11, v. 54, no. 1 p. 229-234.

Abstract: Angiotensin converting enzyme (ACE) activity was evaluated in the presence of flavanol-rich foods, i.e., wines, chocolates, and teas, and of purified flavonoids. All foods assayed inhibited ACE activity, red wines being more effective than white wine, and green tea more effective than black tea. The inhibition of ACE activity was associated with both phenolic and flavanol content in the foods. When isolated polyphenols were assayed, procyanidins (dimer and hexamer) and epigallocatechin significantly inhibited enzyme activity; similar concentrations of (+)-catechin, (-)-epicatechin, gallic acid, chlorogenic acid, caffeic acid, quercetin, kaempferol, and resveratrol were ineffective. When ACE activity was assayed in rat kidney membranes in the presence of chocolate extracts or purified procyanidins, it was observed that the inhibition depended on the chocolate content of flavanols and the number of flavanol units constituting the procyanidin. These experiments demonstrate that flavanols either isolated or present in foods could inhibit ACE activity. The occurrence of such inhibition in vivo needs to be determined, although is supported by the association between the consumption of flavanol-rich foods and reductions in blood pressure observed in several experimental models.


Specific killing of multiple myeloma cells by (-)-epigallocatechin-3-gallate extracted from green tea: biologic activity and therapeutic implications.
Author: Shammas,-M-A; Neri,-P; Koley,-H; Batchu,-R-B; Bertheau,-R-C; Munshi,-V; Prabhala,-R; Fulciniti,-M; Tai,-Y-T; Treon,-S-P; Goyal,-R-K; Anderson,-K-C; Munshi,-N-C
Citation: Blood. 2006 Oct 15; 108(8): 2804-10

Abstract: Epigallocatechin-3-gallate (EGCG), a polyphenol extracted from green tea, is an antioxidant with chemopreventive and chemotherapeutic actions. Based on its ability to modulate growth factor-mediated cell proliferation, we evaluated its efficacy in multiple myeloma (MM). EGCG induced both dose- and time-dependent growth arrest and subsequent apoptotic cell death in MM cell lines including IL-6-dependent cells and primary patient cells, without significant effect on the growth of peripheral blood mononuclear cells (PBMCs) and normal fibroblasts. Treatment with EGCG also led to significant apoptosis in human myeloma cells grown as tumors in SCID mice. EGCG interacts with the 67-kDa laminin receptor 1 (LR1), which is significantly elevated in myeloma cell lines and patient samples relative to normal PBMCs. RNAi-mediated inhibition of LR1 resulted in abrogation of EGCG-induced apoptosis in myeloma cells, indicating that LR1 plays an important role in mediating EGCG activity in MM while sparing PBMCs. Evaluation of changes in gene expression profile indicates that EGCG treatment activates distinct pathways of growth arrest and apoptosis in MM cells by inducing the expression of death-associated protein kinase 2, the initiators and mediators of death receptor-dependent apoptosis (Fas ligand, Fas, and caspase 4), p53-like proteins (p73, p63), positive regulators of apoptosis and NF-kappaB activation (CARD10, CARD14), and cyclin-dependent kinase inhibitors (p16 and p18). Expression of related genes at the protein level were also confirmed by Western blot analysis. These data demonstrate potent and specific antimyeloma activity of EGCG and provide the rationale for its clinical evaluation.





Modulatory efficacy of green tea polyphenols on glycoconjugates and immunological markers in 4-Nitroquinoline 1-oxide-induced oral carcinogenesis-A therapeutic approach.
Author: Srinivasan,-P; Sabitha,-K-E; Shyamaladevi,-C-S
 Citation: Chem-Biol-Interact. 2006 Aug 25; 162(2): 149-56

Abstract: Green tea polyphenols (GTP) has been used as a chemopreventive agent world wide against chemically induced cancer. The present study is aimed to understand the therapeutic action of GTP on glycoconjugates and immunological markers in 4-Nitroquinoline 1-oxide (4-NQO)-induced oral cancer over a period of 30 days at 200mg/kg, p.o., Oral cancer was induced by painting 4-NQO for 8 weeks followed by administration of GTP after 22 weeks, for 30 days. Glycoconjugates such as hexose, hexosamine, sialicacid, fucose and mucoprotein were analysed. Expression of glycoconjugates was examined through histology and SDS-PAGE. Immunological markers such as circulating immune complex and mast cell density were studied. Oral cancer-induced animals showed a significant increase in levels of glycoconjugates and its expression, similar to that observed for immunological markers. Treatment with GTP altered the expression of glycoconjugates as well as immunological markers. The results suggest that GTP modulates both the expression of glycoconjugates and immunological markers resulting in regression of oral cancer.



Therapeutic effect of green tea extract on oxidative stress in aorta and heart of streptozotocin diabetic rats.
Author: Babu,-P-V; Sabitha,-K-E; Shyamaladevi,-C-S
Citation: Chem-Biol-Interact. 2006 Aug 25; 162(2): 114-20

Abstract: Hyperglycemia induced oxidative stress has been proposed as a cause of many complications of diabetes including cardiac dysfunction. The present study depicts the therapeutic effect of green tea extract on oxidative stress in aorta as well as heart of streptozotocin diabetic rats. Six weeks after diabetes induction, green tea was administered orally for 4 weeks [300 mg (kg body weight)(-1) day (-1)]. In aorta and heart of diabetic rats there was a significant increase in the activity of superoxide dismutase, catalase and glutathione peroxidase with an increase in lipid peroxides. Diabetic rats showed a significant decrease in the levels of serum and cardiac glutathione. Green tea administration to diabetic rats reduced lipid peroxides and activity of antioxidant enzymes whereas increased glutathione content. The results demonstrate that the induction of antioxidant enzymes in diabetic rats is not efficient and sufficient to reduce the oxidative stress. But green tea by providing a competent antioxidative mechanism ameliorates the oxidative stress in the aorta and heart of diabetic rats. The study suggests that green tea may provide a useful therapeutic option in the reversal of oxidative stress induced cardiac dysfunction in diabetes mellitus.



Epigallocatechin gallate supplementation alleviates diabetes in rodents.
Author: Wolfram,-S; Raederstorff,-D; Preller,-M; Wang,-Y; Teixeira,-S-R; Riegger,-C; Weber,-P
Citation: J-Nutr. 2006 Oct; 136(10): 2512-8

Abstract: As the prevalence of type 2 diabetes mellitus is increasing at an alarming rate, effective nutritional and exercise strategies for the prevention of this disease are required. Specific dietary components with antidiabetic efficacy could be one aspect of these strategies. This study investigated the antidiabetic effects of the most abundant green tea catechin, epigallocatechin gallate (EGCG, TEAVIGO), in rodent models of type 2 diabetes mellitus and H4IIE rat hepatoma cells. We assessed glucose and insulin tolerance in db/db mice and ZDF rats after they ingested EGCG. Using gene microarray and real-time quantitative RT-PCR we investigated the effect of EGCG on gene expression in H4IIE rat hepatoma cells as well as in liver and adipose tissue of db/db mice. EGCG improved oral glucose tolerance and blood glucose in food-deprived rats in a dose-dependent manner. Plasma concentrations of triacylglycerol were reduced and glucose-stimulated insulin secretion was enhanced. In H4IIE cells, EGCG downregulated genes involved in gluconeogenesis and the synthesis of fatty acids, triacylgycerol, and cholesterol. EGCG decreased the mRNA expression of phosphoenolpyruvate carboxykinase in H4IIE cells as well as in liver and adipose tissue of db/db mice. Glucokinase mRNA expression was upregulated in the liver of db/db mice in a dose-dependent manner. This study shows that EGCG beneficially modifies glucose and lipid metabolism in H4IIE cells and markedly enhances glucose tolerance in diabetic rodents. Dietary supplementation with EGCG could potentially contribute to nutritional strategies for the prevention and treatment of type 2 diabetes mellitus.



Tea flavanols inhibit angiotensin-converting enzyme activity and increase nitric oxide production in human endothelial cells.
Author: Persson,-I-A; Josefsson,-M; Persson,-K; Andersson,-R-G
Citation: J-Pharm-Pharmacol. 2006 Aug; 58(8): 1139-44

Abstract: A diversity of pharmacological effects on the cardiovascular system have been reported for Camellia sinensis: antioxidative, antiproliferative and anti-angiogenic activity, and nitric oxide synthase activation. The purpose of this study was to investigate if the connection between tea and angiotensin-converting enzyme (ACE) and nitric oxide (NO) might be an explanation of the pharmacological effects of tea on the cardiovascular system. Cultured endothelial cells from human umbilical veins (HUVEC) were incubated with extracts of Japanese Sencha (green tea), Indian Assam Broken Orange Pekoe (black tea) and Rooibos tea, respectively. The main flavanols and purine alkaloids in green and black tea were examined for their effects on ACE and NO. After incubation with green tea, black tea and Rooibos tea for 10 min, a significant and dose-dependent inhibition of ACE activity in HUVEC was seen with the green tea and the black tea. No significant effect on ACE was seen with the Rooibos tea. After 10-min incubation with (-)-epicatechin, (-)-epigallocatechin, (-)-epicatechingallate and (-)-epigallocatechingallate, a dose-dependent inhibition of ACE activity in HUVEC was seen for all four tea catechins. After 24-h incubation, a significantly increased dose-dependent effect on NO production in HUVEC was seen for the green tea, the black tea and the Rooibos tea. After 24-h incubation with (-)-epicatechin, (-)-epigallocatechin, (-)-epicatechingallate and (-)-epigallocatechingallate, a dose-dependent increased NO production in HUVEC was seen. In conclusion, tea extracts from C. sinensis may have the potential to prevent and protect against cardiovascular disease.



Green tea extract induces interleukin-8 (IL-8) mRNA and protein expression but specifically inhibits IL-8 secretion in caco-2 cells.
Author: Netsch,-M-I; Gutmann,-H; Aydogan,-C; Drewe,-J
Citation: Planta-Med. 2006 Jun; 72(8): 697-702

Abstract: The chemokine interleukin (IL)-8 is a cytokine involved in neutrophil attraction and activation and elevated levels have been observed in intestinal inflammation. Anti-inflammatory activities have been attributed to green tea or its major constituent (-)-epigallocatechin gallate (EGCG). In this study, we investigated the effects of a defined green tea extract (GTE) or EGCG on basal or IL-1beta-induced IL-8 expression and secretion in the human gastrointestinal epithelial cell line Caco-2. mRNA expression levels were determined by quantitative RT-PCR. GTE significantly induced IL-8 mRNA expression, which was not mediated indirectly via an induction of IL-1beta mRNA expression. EGCG only exerted a weak although significant induction of IL-8 mRNA expression at the highest concentration. Intracellular and extracellular protein levels were analyzed by an enzyme-linked immunosorbent assay. GTE and EGCG significantly decreased secreted IL-8 concentrations. Determination of intracellular and secreted IL-8 concentrations after 24 h, 48 h, and 72 h of incubation suggested that GTE specifically inhibited IL-8 secretion while inducing DE NOVO synthesis of IL-8. The IL-1beta-mediated increase of IL-8 secretion was significantly inhibited by GTE in a dose-dependent manner. At the highest concentration, GTE inhibited IL-1beta-induced IL-8 secretion to a similar extent as found for brefeldin A, an inhibitor of vesicular transport. These results suggest that GTE may exert an anti-inflammatory activity in enterocytes, which may be useful for the treatment of intestinal inflammation.


Bioassay-guided purification and identification of antimicrobial components in Chinese green tea extract.
 Author: Si,-W; Gong,-J; Tsao,-R; Kalab,-M; Yang,-R; Yin,-Y
Citation: J-Chromatogr-A. 2006 Sep 1; 1125(2): 204-10
Abstract: The Chinese green tea extract was found to strongly inhibit the growth of major food-borne pathogens, Escherichia coli O157:H7, Salmonella Typhimurium DT104, Listeria monocytogenes, Staphylococcus aureus, and a diarrhoea food-poisoning pathogen Bacillus cereus, by 44-100% with the highest activity found against S. aureus and lowest against E. coli O157:H7. A bioassay-guided fractionation technique was used for identifying the principal active component. A simple and efficient reversed-phase high-speed counter-current chromatography (HSCCC) method was developed for the separation and purification of four bioactive polyphenol compounds, epicatechin gallate (ECG), epigallocatechin gallate (EGCG), epicatechin (EC), and caffeine (CN). The structures of these polyphenols were confirmed with mass spectrometry. Among the four compounds, ECG and EGCG were the most active, particularly EGCG against S. aureus. EGCG had the lowest MIC90 values against S. aureus (MSSA) (58 mg/L) and its methicilin-resistant S. aureus (MRSA) (37 mg/L). Scanning electron microscopy (SEM) studies showed that these two compounds altered bacterial cell morphology, which might have resulted from disturbed cell division. This study demonstrated a direct link between the antimicrobial activity of tea and its specific polyphenolic compositions. The activity of tea polyphenols, particularly EGCG on antibiotics-resistant strains of S. aureus, suggests that these compounds are potential natural alternatives for the control of bovine mastitis and food poisoning caused by S. aureus.



Effects of green tea on urinary stone formation: an in vivo and in vitro study.
Author: Jeong,-B-C; Kim,-B-S; Kim,-J-I; Kim,-H-H
Citation: J-Endourol. 2006 May; 20(5): 356-61

Abstract: PURPOSE: We evaluated whether epigallocatechin gallate (EGCG), a main constituent of green tea polyphenols, could protect against cellular toxicity by oxalate and whether green tea supplementation attenuates the development of nephrolithiasis in an animal model. MATERIALS AND METHODS: Cells of the NRK-52E line were incubated with different concentrations of oxalate with and without EGCG, and toxicity and malondialdehyde assays were done to investigate the cytotoxic effect of oxalate and the anti-oxalate effect of EGCG.. In a second series of experiments, male Sprague-Dawley rats were divided into three groups. Group 1 animals (controls) were fed regular chow and drank water ad libitum; group 2 animals were fed chow containing 3% sodium oxalate with the administration of gentamicin (40 mg/kg) and drank water ad libitum; group 3 animals were fed the same diet as group 2 with gentamicin administration and drank only green tea. Rats were killed 4 weeks later after a 24-hour urine collection, and the kidneys were removed for morphologic examination. RESULTS: As oxalate concentrations increased, the number of surviving cells decreased, and the formation of free radicals increased. The administration of EGCG inhibited free-radical production induced by oxalate. Green tea supplementation decreased the excretion of urinary oxalate and the activities of urinary gammaglutamyltranspeptidase and N-acetylglucosaminidase. The number of crystals within kidneys in group 3 was significantly lower than in group 2. CONCLUSIONS: Green tea has an inhibitory effect on urinary stone formation, and the antioxidative action of EGCG is considered to be involved.

 

Effect of green tea consumption on endothelial function and circulating endothelial progenitor cells in chronic smokers.
Author: Kim,-W; Jeong,-M-H; Cho,-S-H; Yun,-J-H; Chae,-H-J; Ahn,-Y-K; Lee,-M-C; Cheng,-X; Kondo,-T; Murohara,-T; Kang,-J-C
Citation: Circ-J. 2006 Aug; 70(8): 1052-7

Abstract: BACKGROUND: The present study was designed to investigate the effect and relationship of endothelial function and endothelial progenitor cells (EPCs) by green tea consumption in chronic smokers. The numbers of circulating EPCs have an inverse correlation with chronic smoking and endothelial dysfunction. Green tea catechin improved endothelial dysfunction in chronic smokers. METHOD AND RESULTS: In 20 young healthy smokers, endothelial functions, defined by flow-mediated endothelium dependent vasodilation (FMD) of the brachial artery via ultrasound as well as the number of EPCs isolated from peripheral blood, were determined at baseline and at 2 weeks after green tea consumption (8 g/day). Circulating EPCs were quantified by flow cytometry as CD45lowCD34+KDR2+ cells and by acyl-low-density lipoprotein and fluorescein isotiocyanate-lectin double positive cells after culture for 7 days. Clinical characteristics and laboratory findings were not significantly different between the baseline and at 2 weeks after green tea intake. EPC levels were inversely correlated with the number of cigarettes smoked. Circulating EPCs by flow cytometry (78.6+/-72.6 vs 156.1+/-135.8 /ml, p<0.001) and cultured EPCs (118.2+/-35.7 vs 169.31+/-58.3/10 field, p<0.001) increased rapidly at 2 weeks after green tea consumption. FMD was significantly improved after 2 weeks (7.2+/-2.8 vs 9.3+/-2.4, p<0.001). The FMD correlated with EPC counts (r=0.67, p=0.003) before treatment and after 2 weeks (r=0.60, p=0.013). CONCLUSIONS: A short-term administration of green tea consumption induces a rapid improvement of EPC levels and FMD. Green tea consumption may be effective to prevent future cardiovascular events in chronic smokers.



Effect of green tea on angiogenesis and severity of atherosclerosis in cholesterol-fed rabbit.
Author: Kavantzas,-N; Chatziioannou,-A; Yanni,-A-E; Tsakayannis,-D; Balafoutas,-D; Agrogiannis,-G; Perrea,-D
Citation: Vascul-Pharmacol. 2006 Jun; 44(6): 461-3

Abstract: BACKGROUND AND AIMS: Since the development of the atherosclerotic plaque requires the growth of new microvessels in the plaque itself (vasa vasorum), we postulated that green tea may exert an anti-atherogenic effect. METHODS AND RESULTS: Thirteen male New Zealand white rabbits were studied for 17 weeks. All rabbits were fed an hypecholesterolemic diet. After 2 weeks of adaptation rabbits were randomly assigned into two groups. Animals in Group A were fed the hypercholesterolemic diet and received plain tap water ad libitum. Animals in Group B were fed with the same diet and furthermore received 2.5% (g/g) green tea for 17 weeks. CONCLUSION: According to our results the atherosclerotic lesions were more severe in Group B than in Group A specimens. Also, the number of VEGF positively stained foam cells and smooth muscle cells of Group B were significantly greater than in Group A. About 30% less plaque was found in Group A than in the control group (Group B). So, our study showed that the consumption of green tea leads to a reduction of atherosclerosis as well as a significant decrease of VEGF expression in the atherosclerotic plaque of rabbit aorta. The hypothesis that probably green tea may produce its anti-atherogenetic effect through an anti-angiogenetic mechanism needs more investigation.


Iron-chelating and free-radical scavenging activities of microwave-processed green tea in iron overload.
Author: Srichairatanakool,-S; Ounjaijean,-S; Thephinlap,-C; Khansuwan,-U; Phisalpong,-C; Fucharoen,-S
Citation: Hemoglobin. 2006; 30(2): 311-27

Abstract: Secondary iron overload is found in beta-thalassemia (thal) patients because of increased dietary iron absorption and multiple blood transfusions. Excessive iron catalyzes free-radical generation, leading to oxidative damage and vital organ dysfunction. Non-transferrin-bound iron (NTBI) detected in thalassemic plasma is highly toxic and chelatable. Though used to treat iron overload, desferrioxamine (DFO) and deferiprone (L1) also have adverse effects. Green tea (GT) shows many pharmacological effects, particularly antioxidative and iron-chelating capacities. This study was performed to investigate the ability of GT extracts to reduce plasma NTBI concentration and oxidative stress in vitro. The Fe(3+) was found to bind to GT crude extract and form a complex. Green tea crude extract time- and dose-dependently decreased plasma NTBI concentration and counteracted the increase of oxidative stress in both Fe(2+)-EDTA-treated human plasma and erythrocytes. Green tea is a bifunctional natural product that could be relevant for management of iron overload and oxidative stress .


Potent suppressive effect of green tea polyphenols on tobacco-induced mutagenicity.

 Author: Santhosh,-K-T; Swarnam,-J; Ramadasan,-K Citation:

Phytomedicine. 2005 Mar; 12(3): 216-20

Abstract: Antimutagenic activity of green tea (Camellia sinensis) was studied using Salmonella typhimurium strains (TA 102) (Ames test). Aqueous tobacco extract was found to be mutagenic to S. typhimurium TA 102 at concentration of 50 mg/plate. Green tea polyphenols was found to inhibit the mutagenicity of tobacco in a concentration-dependent manner. Concentrations needed for 50% inhibition of mutagen-induced revertant formation was found to be 5 mg/plate. Green tea polyphenols was also found to inhibit the urinary mutagenicity in rats induced by tobacco extract. Moreover green tea polyphenols were found to inhibit in vitro nitrosation reaction produced by reaction sodium nitrite and methyl urea and further inhibition of mutagenicity indicating that green tea has dual action to bring out a reduction in the mutagenic and carcinogenic potential of tobacco.


Molecular and cellular effects of green tea on oral cells of smokers: a pilot study.
Author: Schwartz,-J-L; Baker,-V; Larios,-E; Chung,-F-L
Citation: Mol-Nutr-Food-Res. 2005 Jan; 49(1): 43-51

Abstract: Studies in cell culture and laboratory animals have shown that green tea and its major component, epigallocatechin-3-gallate, inhibit cell growth and reduce tumor incidence. However, results of epidemiological studies have generated inconsistent, sometimes conflicting data regarding protection by green tea against human cancers. To clarify the findings of these laboratory studies in application to humans, we conducted a pilot intervention study with three heavy smokers (> 10 cigarettes/day) and three nonsmokers (never smokers) in order to evaluate the molecular and cellular effects of drinking green tea using human oral cells as an investigative tool. Green tea total extract (400-500 mg/cup, 5 cups/day) was administered in drinking water to the subjects for four weeks. Two oral cytology samples were taken weekly for measurements of tobacco carcinogen-induced DNA damage, including bulky adducts and oxidized bases, cell growth, DNA content, and apoptosis. The study showed that during the course of green tea administration smoking-induced DNA damage was decreased, cell growth was inhibited, and the percentage of cells in S phase was reduced, cells accumulated in G1 phase (cyclin D1 positive), DNA content became more diploid and less aneuploid, and p53, Caspase-3, and TUNEL, markers of apoptosis, were increased. The study, although preliminary, indicates that drinking green tea reduced the number of damaged cells in smokers by inducing cell growth arrest and apoptosis, a mechanism similar to that observed in cultured cells and animals. These results warrant a large-scale intervention trial to further verify the role of green tea in the prevention of oral cancer in smokers.


Protective effect of green tea on erythrocyte membrane of different age rats intoxicated with ethanol.
Author: Dobrzynska,-I; Szachowicz-Petelska,-B; Ostrowska,-J; Skrzydlewska,-E; Figaszewski,-Z
Citation: Chem-Biol-Interact. 2005 Sep 10; 156(1): 41-53

Abstract: It is known that aging is characterized by changes in cell metabolism resulting in modification of the structure and function of cell membrane components which is mainly the consequence of reactive oxygen species action. These disturbances are also enhanced by different xenobiotics, e.g. ethanol. Therefore, the aim of this paper is to examine green tea influence on total antioxidant status (TAS) and on composition and electric charge of erythrocyte membrane phospholipids in ethanol intoxicated rats of various ages. Antioxidant abilities of erythrocytes were estimated by measuring TAS. Qualitative and quantitative composition of phospholipids in the membrane was determined by HPLC, while the extent of erythrocytes lipid peroxidation was estimated by HPLC measurement of malondialdehyde (MDA) and 4-hydroxynonenal (4-HNE) levels. Electrophoresis was used to determine the surface charge density of the rat erythrocyte membrane. It was shown that the process of aging was accompanied by a decrease in TAS and in the total amount of phospholipids as well as by enhancement of lipid peroxidation and increase in surface charge density of erythrocyte membrane. Ethanol administration caused, in term, decrease in TAS and increase in the level of all phospholipids and lipid peroxidation products. Ethanol as well significantly enhanced changes in surface charge density of erythrocyte membrane. The ingestion of green tea partially prevented decrease in erythrocyte antioxidant abilities observed during aging and ethanol intoxication. Moreover, long-term drinking of green tea protects the structure of the erythrocytes membrane disturbed during aging process and/or chronic ethanol intoxication.



Effectiveness of green tea catechines for the correction of the alimentary obesity in the experiment.

Author: Chanadiri,-T; Sanikidze,-T; Esaishvili,-M; Chkhikvishvili,-I; Datunashvili,-I
Citation: Georgian-Med-News. 2005 Sep; (9): 61-3

Abstract: Obesity is one of the most important problems of the modern medicine. The immobile life-style and consumption of high-calorie food are the most remarkable risk-factors of the obesity, which in presence of genetic predisposition contribute to the increasing of the body weight. In the modern literature there are numerous data about the important role of free radical oxidation in the pathogenesis of the obesity. In this relation application of natural antioxidants for the purpose of the correction of excess weight has gained an active research interest. Numerous researches showed natural antioxidants to be effective in correction of elevated blood cholesterol, triglycerides and LDL levels. In this relation the purpose of our research was to investigate effectiveness of green tea catechizes on lipid metabolism disorder, antioxidant status and excess body weight during experimental alimentary obesity. Experiment was conducted on rats kept on high-calorie diet for 7 weeks. Simultaneously one group of animals had been administered catechines in addition to the high-calorie diet during last 4 weeks. The experiment established corrective effect of catechines on the parameters of lipid metabolism (blood cholesterol, triglyceride and LDL levels), epididymal fat mass and antioxidant enzymes activity. Obtained results may be important for the development of weight losing diets.


Green tea polyphenol extract attenuates ischemia/reperfusion injury of the gut.
Author: Muia,-C; Mazzon,-E; Di-Paola,-R; Genovese,-T; Menegazzi,-M; Caputi,-A-P; Suzuki,-H; Cuzzocrea,-S
Citation: Naunyn-Schmiedebergs-Arch-Pharmacol. 2005 May; 371(5): 364-74
Abstract: Various studies have clearly demonstrated that green tea catechins possess potent antioxidative properties, and the preventive effects against various oxidative diseases have been reported. The aim of this study was to investigate the effect of green tea extract on the tissue injury caused by ischemia/reperfusion (I/R) of the gut. I/R injury of the intestine was caused by clamping both the superior mesenteric artery and the celiac trunk for 45 min followed by release of the clamp allowing reperfusion for 1 h or 4 h. This procedure results in splanchnic artery occlusion (SAO) shock. Rats subjected to SAO developed a significant fall in mean arterial blood pressure, and only 10% of the animals survived for the entire 4-h reperfusion period. Surviving animals were sacrificed for histological examination and biochemical studies. Rats subjected to SAO displayed a significant increase in tissue myeloperoxidase (MPO) activity and malondialdehyde (MDA) levels, significant increases in plasma tumor necrosis factor (TNF)-alpha levels and marked injury to the distal ileum. Increased immunoreactivity to nitrotyrosine was observed in the ileum of rats subjected to SAO. Staining of sections of the ileum obtained from SAO rats with anti-intercellular adhesion molecule (ICAM-1) antibody and with anti-P-selectin antibody resulted in diffuse staining. Administration of green tea extract (20 and 10 mg kg(-1) i.v.) 15 min prior to the onset of gut reperfusion significantly reduced in a dose-dependent manner the fall in mean arterial blood pressure, the mortality rate, infiltration of the reperfused intestine with polymorphonuclear neutrophils (MPO activity), lipid peroxidation (MDA levels), production of TNF-alpha, and histological evidence of gut injury. Administration of green tea extract also markedly reduced nitrotyrosine formation and the up-regulation of ICAM-1 and P-selectin during reperfusion. In order to clarify that green tea extract might be useful in the therapy of I/R injury, we also investigated the effect of green tea extract (20 mg kg(-1) i.v.) when administered 5 min after the onset of gut reperfusion. Similar to the pretreatment approach, the post-treatment also significantly reduced the gut injury induced by I/R. These results demonstrate that green tea extract significantly reduces I/R injury of the intestine.


Impact of diet on prostate cancer: a review.
Author: Sonn,-G-A; Aronson,-W; Litwin,-M-S
Citation: Prostate-Cancer-Prostatic-Dis. 2005; 8(4): 304-10
Abstract: Epidemiological studies suggest that environmental factors may mediate the transformation of latent prostate cancer into clinically apparent tumors and that diet appears to influence this progression. Close correlations between average per capita fat intake and prostate cancer mortality internationally generated interest in underlying mechanisms for this link, such as through serum levels of androgens, free radicals, proinflammatory fatty acid metabolites, or insulin-like growth factor. Much interest currently lies in the potential of HMG-CoA reductase inhibitors (statins) to play a chemopreventative role in prostate cancer. Lycopene, a potent antioxidant found in tomatoes, may exert a protective effect in the prostate. Selenium and vitamin E have also been shown to decrease the risk of prostate cancer in some men. Calcium may support vitamin D-related antiproliferative effects in prostate cancer. Certain soy proteins, common in the Asian diet, have been shown to inhibit prostate cancer cell growth. Finally, green tea may also have a chemopreventive effect by inducing apoptosis. Despite confounding factors present in clinical studies assessing the effect of diet on cancer risk, the data remain compelling that a variety of nutrients may prevent the development and progression of prostate cancer.




Modulation of N-methyl-N-nitrosourea induced mammary tumors in Sprague-Dawley rats by combination of lysine, proline, arginine, ascorbic acid and green tea extract.
Author: Roomi,-M-W; Roomi,-N-W; Ivanov,-V; Kalinovsky,-T; Niedzwiecki,-A; Rath,-M
Citation: Breast-Cancer-Res. 2005; 7(3): R291-5
Abstract: INTRODUCTION: The limited ability of current treatments to control metastasis and the proposed antitumor properties of specific nutrients prompted us to examine the effect of a specific formulation (nutrient supplement [NS]) of lysine, proline, arginine, ascorbic acid, and green tea extract in vivo on the development of N-methyl-N-nitrosourea (MNU)-induced mammary tumors in rats. METHODS: A single intraperitoneal dose of MNU was injected into each of 20 female Sprague-Dawley rats (aged 50 days) to induce tumors. Two weeks after MNU treatment, a time by which the animals had recovered from MNU-induced toxicity, the rats were divided into two groups. Rats in group 1 (n = 10) were fed Purina chow diet, whereas those in group 2 (n = 10) were fed the same diet supplemented with 0.5% NS. After a further 24 weeks, the rats were killed and tumors were excised and processed. RESULTS: NS reduced the incidence of MNU-induced mammary tumors and the number of tumors by 68.4%, and the tumor burden by 60.5%. The inhibitory effect of NS was also reflected by decreased tumor weight; the tumor weights per rat and per group were decreased by 41% and 78%, respectively. In addition, 30% of the control rats developed ulcerated tumors, in contrast to 10% in the nutrient supplemented rats. CONCLUSION: These findings suggest that the specific formulation of lysine, proline, arginine, ascorbic acid, and green tea extract tested significantly reduces the incidence and growth of MNU-induced mammary tumors, and therefore has strong potential as a useful therapeutic regimen for inhibiting breast cancer development.



Green tea with a high catechin content suppresses inflammatory cytokine expression in the galactosamine-injured rat liver.
Author: Abe,-K; Ijiri,-M; Suzuki,-T; Taguchi,-K; Koyama,-Y; Isemura,-M
Citation: Biomed-Res. 2005 Oct; 26(5): 187-92
Abstract: Galactosamine is known to induce hepatic injury in rats and the galactosamine-induced hepatitis is believed to be similar to viral hepatitis both morphologically and functionally. In the present study, we examined how drinking green tea affects the gene expression of inflammatory cytokines which may be up-regulated in galactosamine-induced hepatitis. As has been reported, galactosamine caused hepatic injury in rats as evidenced by an increase in serum transaminase activities and histological observations of the liver. The results of the reverse transcription and polymerase chain reaction indicated an increased gene expression of inflammatory cytokines, tumor necrosis factor-alpha and interleukin-1beta, in the injured liver and the enzyme linked immunoassay showed an increase in the serum levels of these cytokines. Oral administration of green tea rich in catechins (Healthya green tea) restored these biomarkers in the galacotsamine-treated rats to near the control levels. These results suggest that the drinking of green tea with a high catechin content may help to prevent and/or attenuate the development of a certain type of hepatitis.


Inhibitory effect of green tea extract on beta-amyloid-induced PC12 cell death by inhibition of the activation of NF-kappaB and ERK/p38 MAP kinase pathway through antioxidant mechanisms.
Author: Lee,-S-Y; Lee,-J-W; Lee,-H; Yoo,-H-S; Yun,-Y-P; Oh,-K-W; Ha,-T-Y; Hong,-J-T
Citation: Brain-Res-Mol-Brain-Res. 2005 Oct 31; 140(1-2): 45-54
Abstract: Beta-amyloid peptide (Abeta) is considered responsible for the pathogenesis of Alzheimer's disease (AD). Several lines of evidence support that Abeta-induced cytotoxicity is mediated through the generation of reactive oxygen species (ROS). Thus, agents that scavenge ROS level may usefully impede the development or progress of AD. Green tea extract has been known to have such antioxidant properties. Our previous studies demonstrate that green tea extract protected ischemia/reperfusion-induced brain cell death by scavenging oxidative damages of macromolecules. In this study, we investigated the effects of green tea extract on Abeta-induced oxidative cell death in cultured rat pheochromocytoma (PC12) cells. PC12 cells treated with Abeta25-35 (10-50 microM) showed intracellular ROS elevation, the formation of 8-oxodG (an oxidized form of DNA), and underwent apoptotic cell death in a dose-dependent manner. Abeta(25-35) treatment upregulated pro-apoptotic p53 at the gene level, and Bax and caspase-3 at the protein level, but downregulated anti-apoptotic Bcl-2 protein. Interestingly, co-treated green tea extract (10-50 microg/ml) dose-dependently attenuated Abeta(25-35) (50 microM)-induced cell death, intracellular ROS levels, and 8-oxodG formation, in addition to p53, Bax, and caspase-3 expression, but upregulated Bcl-2. Furthermore, green tea extract prevented the Abeta(25-35)-induced activations of the NF-kappaB and ERK and p38 MAP kinase pathways. Our study suggests that green tea extract may usefully prevent or retard the development and progression of AD.


A review of antioxidants and Alzheimer's disease.
Author: Frank,-B; Gupta,-S
Citation: Ann-Clin-Psychiatry. 2005 Oct-Dec; 17(4): 269-86
Abstract: BACKGROUND: In this article, we review a diverse body of research and draw conclusions about the usefulness, or lack there-of, of specific antioxidants in the prevention of Alzheimer's disease (AD). METHODS: The National Library of Medicine's database was searched for the years 1996-2004 using the search terms "Alzheimer's, anti-oxidants, antioxidants." RESULTS: Over 300 articles were identified and 187 articles were selected for inclusion based on relevance to the topic. Agents that show promise in helping prevent AD include: 1) aged garlic extract, 2) curcumin, 3) melatonin, 4) resveratrol, 5) Ginkgo biloba extract, 6) green tea, 7) vitamin C and 8) vitami