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

被引:466
作者
Bose, Mousumi [1 ]
Lambert, Joshua D. [1 ]
Ju, Jihyeung [1 ]
Reuhl, Kenneth R. [2 ]
Shapses, Sue A. [3 ]
Yang, Chung S. [1 ]
机构
[1] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Biol Chem, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmacol & Toxicol, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Grad Program Nutr Sci, New Brunswick, NJ 08901 USA
关键词
D O I
10.1093/jn/138.9.1677
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
In this study, we investigated the effects of the major green tea polypherol, (-)-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). l treatment also decreased liver weight, liver triglycerides, and plasma alanine aminotrarsferase 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 l 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.
引用
收藏
页码:1677 / 1683
页数:7
相关论文
共 38 条
[1]   Green tea extract protects leptin-deficient, spontaneously obese mice from hepatic steatosis and injury1,2 [J].
Bruno, Richard S. ;
Dugan, Christine E. ;
Smyth, Joan A. ;
DiNatale, Dana A. ;
Koo, Sung I. .
JOURNAL OF NUTRITION, 2008, 138 (02) :323-331
[2]   Metabolic syndrome - A comprehensive perspective based on interactions between obesity, diabetes, and inflammation [J].
Dandona, P ;
Aljada, A ;
Chaudhuri, A ;
Mohanty, P ;
Garg, R .
CIRCULATION, 2005, 111 (11) :1448-1454
[3]   Prevention and treatment of the metabolic syndrome [J].
Daskalopoulou, SS ;
Mikhailidis, DP ;
Elisaf, A .
ANGIOLOGY, 2004, 55 (06) :589-612
[4]  
Dulloo AG, 1999, AM J CLIN NUTR, V70, P1040
[5]   Nonalcoholic fatty liver disease: From steatosis to cirrhosis [J].
Farrell, GC ;
Larter, CZ .
HEPATOLOGY, 2006, 43 (02) :S99-S112
[6]   (-)-Epigallocatechin-3-gallate inhibits monocyte chemotactic protein-1 expression in endothelial cells via blocking NF-κB signaling [J].
Hong, Min H. ;
Kim, Mi H. ;
Chang, Hee J. ;
Kim, Nam H. ;
Shin, Boo A. ;
Ahn, Bong W. ;
Jung, Young D. .
LIFE SCIENCES, 2007, 80 (21) :1957-1965
[7]   Antihyperglycentic effect of oolong tea in type 2 diabetes [J].
Hosoda, K ;
Wang, MF ;
Liao, ML ;
Chuang, CK ;
Iha, M ;
Clevidence, B ;
Yamamoto, S .
DIABETES CARE, 2003, 26 (06) :1714-1718
[8]   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 [J].
Ikeda, I ;
Hamamoto, R ;
Uzu, K ;
Imaizumi, K ;
Nagao, K ;
Yanagita, T ;
Suzuki, Y ;
Kobayashi, M ;
Kakuda, T .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2005, 69 (05) :1049-1053
[9]   CROSS-SECTIONAL STUDY OF EFFECTS OF DRINKING GREEN TEA ON CARDIOVASCULAR AND LIVER-DISEASES [J].
IMAI, K ;
NAKACHI, K .
BRITISH MEDICAL JOURNAL, 1995, 310 (6981) :693-696
[10]   MCP-1 contributes to macrophage infiltration into adipose tissue, insulin resistance, and hepatic steatosis in obesity [J].
Kanda, Hajime ;
Tateya, Sanshiro ;
Tamori, Yoshikazu ;
Kotani, Ko ;
Hiasa, Ken-ichi ;
Kitazawa, Riko ;
Kitazawa, Sohei ;
Miyachi, Hitoshi ;
Maeda, Sakan ;
Egashira, Kensuke ;
Kasuga, Masato .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (06) :1494-1505