Hepatotoxicity of high oral dose (-)-epigallocatechin-3-gallate in mice

被引:336
作者
Lambert, Joshua D. [1 ]
Kennett, Mary J. [2 ]
Sang, Shengmin [3 ]
Reuhl, Kenneth R. [4 ]
Ju, Jihyeung [5 ]
Yang, Chung S. [5 ]
机构
[1] Penn State Univ, Dept Food Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Vet Sci, University Pk, PA 16802 USA
[3] N Carolina Cent Univ, Human Nutr Program, Biomed Biotechnol Res Inst, Kannapolis, NC 28081 USA
[4] Rutgers State Univ, Dept Pharmacol & Toxicol, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
[5] Rutgers State Univ, Dept Biol Chem, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院;
关键词
Green tea; (-)-Epigallocatechin-3-gallate; Hepatotoxicity; Mouse; Oxidative stress; GREEN TEA POLYPHENOL; CATECHINS; CANCER; LIVER; INHIBITION; ENZYMOLOGY; EXTRACT; DISEASE; GALLATE;
D O I
10.1016/j.fct.2009.10.030
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) has been studied for chronic disease preventive effects, and is marketed as part of many dietary supplements. However, case-reports have associated the use of green tea-based supplements with liver toxicity. We studied the hepatotoxic effects of high dose EGCG in male CF-1 mice. A single dose of EGCG (1500 mg/kg, i.g.) increased plasma alanine aminotransferase (ALT) by 138-fold and reduced survival by 85%. Once-daily dosing with EGCG increased hepatotoxic response. Plasma ALT levels were increased 184-fold following two once-daily doses of 750 mg/kg, i.g. EGCG. Moderate to severe hepatic necrosis was observed following treatment with EGCG. EGCG hepatotoxicity was associated with oxidative stress including increased hepatic lipid peroxidation (5-fold increase), plasma 8-isoprostane (9.5-fold increase) and increased hepatic metallothionein and gamma-histone 2AX protein expression. EGCG also increased plasma interleukin-6 and monocyte chemoattractant protein-1. Our results indicate that higher bolus doses of EGCG are hepatotoxic to mice. Further studies on the dose-dependent hepatotoxic effects of EGCG and the underlying mechanisms are important given the increasing use of green tea dietary supplements. which may deliver much higher plasma and tissue concentrations of EGCG than tea beverages. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:409 / 416
页数:8
相关论文
共 35 条
[1]
The chemistry of tea flavonoids [J].
Balentine, DA ;
Wiseman, SA ;
Bouwens, LCM .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) :693-704
[2]
Baltaziak Marek, 2004, Folia Morphol (Warsz), V63, P123
[3]
Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: A preliminary report from a one-year proof-of-principle study [J].
Bettuzzi, S ;
Brausi, M ;
Rizzi, F ;
Castagnetti, G ;
Peracchia, G ;
Corti, A .
CANCER RESEARCH, 2006, 66 (02) :1234-1240
[4]
Hepatotoxicity associated with supplements containing Chinese green tea (Camellia sinensis) [J].
Bonkovsky, HL .
ANNALS OF INTERNAL MEDICINE, 2006, 144 (01) :68-71
[5]
The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice [J].
Bose, Mousumi ;
Lambert, Joshua D. ;
Ju, Jihyeung ;
Reuhl, Kenneth R. ;
Shapses, Sue A. ;
Yang, Chung S. .
JOURNAL OF NUTRITION, 2008, 138 (09) :1677-1683
[6]
Role of IL-6 in an IL-10 and IL-4 double knockout mouse model uniquely susceptible to acetaminophen-induced liver injury [J].
Bourdi, Mohammed ;
Eiras, Daniel P. ;
Holt, Michael P. ;
Webster, Marie R. ;
Reilly, Timothy P. ;
Welch, Kevin D. ;
Pohl, Lance R. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2007, 20 (02) :208-216
[7]
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
[8]
Chen JH, 2004, AM J CLIN NUTR, V80, P742
[9]
Chen LS, 1997, DRUG METAB DISPOS, V25, P1045
[10]
Effects of repeated green tea catechin administration on human cytochrome P450 activity [J].
Chow, H-H. Sherry ;
Hakim, Iman A. ;
Vining, Donna R. ;
Crowell, James A. ;
Cordova, Catherine A. ;
Chew, Wade M. ;
Xu, Min-Jian ;
Hsu, Chiu-Hsieh ;
Ranger-Moore, James ;
Alberts, David S. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (12) :2473-2476