The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice.

In this study, we investigated the effects of the major green tea polyphenol, (-)-epigallocatechin-3-gallate (EGCG), on high-fat-induced obesity, symptoms of the metabolic syndrome, and fatty liver in mice. In mice fed a high-fat diet (60% energy as fat), supplementation with dietary EGCG treatment (3.2 g/kg diet) for 16 wk reduced body weight (BW) gain, percent body fat, and visceral fat weight (P < 0.05) compared with mice without EGCG treatment. The BW decrease was associated with increased fecal lipids in the high-fat-fed groups (r(2) = 0.521; P < 0.05). EGCG treatment attenuated insulin resistance, plasma cholesterol, and monocyte chemoattractant protein concentrations in high-fat-fed mice (P < 0.05). EGCG treatment also decreased liver weight, liver triglycerides, and plasma alanine aminotransferase concentrations in high-fat-fed mice (P < 0.05). Histological analyses of liver samples revealed decreased lipid accumulation in hepatocytes in mice treated with EGCG compared with high-fat diet-fed mice without EGCG treatment. In another experiment, 3-mo-old high-fat-induced obese mice receiving short-term EGCG treatment (3.2 g/kg diet, 4 wk) had decreased mesenteric fat weight and blood glucose compared with high-fat-fed control mice (P < 0.05). Our results indicate that long-term EGCG treatment attenuated the development of obesity, symptoms associated with the metabolic syndrome, and fatty liver. Short-term EGCG treatment appeared to reverse preexisting high-fat-induced metabolic pathologies in obese mice. These effects may be mediated by decreased lipid absorption, decreased inflammation, and other mechanisms.

[1]  R. Bruno,et al.  Green tea extract protects leptin-deficient, spontaneously obese mice from hepatic steatosis and injury. , 2008, The Journal of nutrition.

[2]  J. Wardle,et al.  The effects of chronic tea intake on platelet activation and inflammation: a double-blind placebo controlled trial. , 2007, Atherosclerosis.

[3]  B. Shin,et al.  (−)-Epigallocatechin-3-gallate inhibits monocyte chemotactic protein-1 expression in endothelial cells via blocking NF-κB signaling , 2007 .

[4]  M. Quon,et al.  EGCG, a green tea polyphenol, improves endothelial function and insulin sensitivity, reduces blood pressure, and protects against myocardial I/R injury in SHR. , 2007, American journal of physiology. Endocrinology and metabolism.

[5]  A. Rudich,et al.  Improved glucose tolerance in mice receiving intraperitoneal transplantation of normal fat tissue , 2007, Diabetologia.

[6]  A. Janež,et al.  Molecular mechanisms of insulin resistance and associated diseases. , 2007, Clinica chimica acta; international journal of clinical chemistry.

[7]  B. Shin,et al.  (-)-Epigallocatechin-3-gallate inhibits monocyte chemotactic protein-1 expression in endothelial cells via blocking NF-kappaB signaling. , 2007, Life sciences.

[8]  S. Kahn,et al.  Review: The role of insulin resistance in nonalcoholic fatty liver disease. , 2006, The Journal of clinical endocrinology and metabolism.

[9]  K. Petersen,et al.  Molecular Mechanisms of Insulin Resistance in Humans and Their Potential Links With Mitochondrial Dysfunction , 2006, Diabetes.

[10]  Ying Wang,et al.  Epigallocatechin gallate supplementation alleviates diabetes in rodents. , 2006, The Journal of nutrition.

[11]  J. Furne,et al.  An extract of black, green, and mulberry teas causes malabsorption of carbohydrate but not of triacylglycerol in healthy volunteers. , 2006, The American journal of clinical nutrition.

[12]  R. Yu,et al.  Mesenteric Adipose Tissue‐Derived Monocyte Chemoattractant Protein‐1 Plays a Crucial Role in Adipose Tissue Macrophage Migration and Activation in Obese Mice , 2006, Obesity.

[13]  T. Tsujita,et al.  Antiobesity action of ϵ-polylysine, a potent inhibitor of pancreatic lipase Published, JLR Papers in Press, May 24, 2006. , 2006, Journal of Lipid Research.

[14]  R. Kitazawa,et al.  MCP-1 contributes to macrophage infiltration into adipose tissue, insulin resistance, and hepatic steatosis in obesity. , 2006, The Journal of clinical investigation.

[15]  G. Farrell,et al.  Nonalcoholic fatty liver disease: From steatosis to cirrhosis , 2006, Hepatology.

[16]  Ying Wang,et al.  Anti-obesity effects of green tea: from bedside to bench. , 2006, Molecular nutrition & food research.

[17]  T. Tsujita,et al.  Antiobesity action of epsilon-polylysine, a potent inhibitor of pancreatic lipase. , 2006, Journal of lipid research.

[18]  S. Klaus,et al.  Epigallocatechin gallate attenuates diet-induced obesity in mice by decreasing energy absorption and increasing fat oxidation , 2005, International Journal of Obesity.

[19]  A. Aljada,et al.  Contemporary Reviews in Cardiovascular Medicine Metabolic Syndrome A Comprehensive Perspective Based on Interactions Between Obesity, Diabetes, and Inflammation , 2022 .

[20]  H. S. Park,et al.  Greater beneficial effects of visceral fat reduction compared with subcutaneous fat reduction on parameters of the metabolic syndrome: a study of weight reduction programmes in subjects with visceral and subcutaneous obesity , 2005, Diabetic medicine : a journal of the British Diabetic Association.

[21]  Ying Wang,et al.  TEAVIGOTM (Epigallocatechin Gallate) Supplementation Prevents Obesity in Rodents by Reducing Adipose Tissue Mass , 2005, Annals of Nutrition and Metabolism.

[22]  T. Yanagita,et al.  Dietary Gallate Esters of Tea Catechins Reduce Deposition of Visceral Fat, Hepatic Triacylglycerol, and Activities of Hepatic Enzymes Related to Fatty Acid Synthesis in Rats , 2005, Bioscience, biotechnology, and biochemistry.

[23]  Y. Komine,et al.  Ingestion of a tea rich in catechins leads to a reduction in body fat and malondialdehyde-modified LDL in men. , 2005, The American journal of clinical nutrition.

[24]  Yukimi Sano,et al.  Effects of green tea on gene expression of hepatic gluconeogenic enzymes in vivo. , 2004, Planta medica.

[25]  S. Daskalopoulou,et al.  Prevention and Treatment of the Metabolic Syndrome , 2004, Angiology.

[26]  T. Sasaoka,et al.  Effect of green tea on blood glucose levels and serum proteomic patterns in diabetic (db/db) mice and on glucose metabolism in healthy humans , 2004, BMC pharmacology.

[27]  D. Befroy,et al.  Mechanism of Hepatic Insulin Resistance in Non-alcoholic Fatty Liver Disease* , 2004, Journal of Biological Chemistry.

[28]  M. Westerterp-Plantenga,et al.  Effects of green tea on weight maintenance after body-weight loss , 2004, British Journal of Nutrition.

[29]  Liang-Yi Wu,et al.  Green tea supplementation ameliorates insulin resistance and increases glucose transporter IV content in a fructose-fed rat model , 2004, European journal of nutrition.

[30]  Chung S. Yang,et al.  Mechanisms of cancer prevention by tea constituents. , 2003, The Journal of nutrition.

[31]  P. Weber,et al.  Effect of EGCG on lipid absorption and plasma lipid levels in rats. , 2003, The Journal of nutritional biochemistry.

[32]  B. Clevidence,et al.  Antihyperglycemic effect of oolong tea in type 2 diabetes. , 2003, Diabetes care.

[33]  S. Rössner,et al.  Obesity: the disease of the twenty-first century , 2002, International Journal of Obesity.

[34]  T. Murase,et al.  Beneficial effects of tea catechins on diet-induced obesity: stimulation of lipid catabolism in the liver , 2002, International Journal of Obesity.

[35]  D. Granner,et al.  Epigallocatechin Gallate, a Constituent of Green Tea, Represses Hepatic Glucose Production* , 2002, The Journal of Biological Chemistry.

[36]  B. Clevidence,et al.  Oolong tea increases metabolic rate and fat oxidation in men. , 2001, The Journal of nutrition.

[37]  A. Dulloo,et al.  Efficacy of a green tea extract rich in catechin polyphenols and caffeine in increasing 24-h energy expenditure and fat oxidation in humans. , 1999, The American journal of clinical nutrition.

[38]  K. Nakachi,et al.  Cross sectional study of effects of drinking green tea on cardiovascular and liver diseases , 1995, BMJ.

[39]  M. Zamboni,et al.  Effect of weight loss on regional body fat distribution in premenopausal women. , 1993, The American journal of clinical nutrition.