A review of the health effects of green tea catechins in in vivo animal models

被引:420
作者
Crespy, V [1 ]
Williamson, G [1 ]
机构
[1] Nestle Res Ctr, CH-1000 Lausanne, Switzerland
关键词
green tea; catechin; epigallocatechin gallate; in vivo animal studies; cancer; cardiovascular disease;
D O I
10.1093/jn/134.12.3431S
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
There is good evidence from in vitro studies that green tea catechins have a role in protection against degenerative diseases. However, the concentrations used in vitro are often higher than those found in animal or human plasma, and so in vivo evidence is required to demonstrate any protective effect of catechins. This article summarizes the most interesting in vivo animal studies on the protective effects of green tea catechins against biomarkers for cancer, cardiovascular disease, and other degenerative diseases. Generally, most studies using animal models show that consumption of green tea (catechins) provides some protection, although most studies have not examined dose response. Tea catechins could act as antitumorigenic agents and as immune modulators in immunodysfunction caused by transplanted tumors or by carcinogen treatment. Green tea has antiproliferative activity in hepatoma cells and hypolipidemic activity in hepatoma-treated rats, and some studies report that it prevents hepatoxicity. It could act as a preventive agent against mammary cancer postinitiation. Nevertheless, the implications of green tea catechins in preventing metastasis have not been clearly established. Long-term feeding of tea catechins could be beneficial for the suppression of high-fat diet-induced obesity by modulating lipid metabolism, could have a beneficial effect against lipid and glucose metabolism disorders implicated in type 2 diabetes, and could also reduce the risk of coronary disease. Further investigations on mechanisms, the nature of the active compounds, and appropriate dose levels are needed.
引用
收藏
页码:3431S / 3440S
页数:10
相关论文
共 74 条
[1]   Catechins from green tea (Camellia sinensis) inhibit bovine and human cartilage proteoglycan and type II collagen degradation in vitro [J].
Adcocks, C ;
Collin, P ;
Buttle, DJ .
JOURNAL OF NUTRITION, 2002, 132 (03) :341-346
[2]   Consumption of green tea protects rats from exercise-induced oxidative stress in kidney and liver [J].
Alessio, HM ;
Hagerman, AE ;
Romanello, M ;
Carando, S ;
Threlkeld, MS ;
Rogers, J ;
Dimitrova, Y ;
Muhammed, S ;
Wiley, RL .
NUTRITION RESEARCH, 2002, 22 (10) :1177-1188
[3]   Subchronic toxicity of 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) in Wistar rats [J].
Vaittinen, SL ;
Komulainen, H ;
Kosma, VM ;
Julkunen, A ;
MakiPaakkanen, J ;
Jansson, K ;
Vartiainen, T ;
Tuomisto, J .
FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (12) :1027-1037
[4]   Effects of black tea, green tea and wine extracts on intestinal carcinogenesis induced by azoxymethane in F344 rats [J].
Caderni, G ;
De Filippo, C ;
Luceri, C ;
Salvadori, M ;
Giannini, A ;
Biggeri, A ;
Remy, S ;
Cheynier, V ;
Dolara, P .
CARCINOGENESIS, 2000, 21 (11) :1965-1969
[5]   Chemopreventive effects of green and black tea on pulmonary and hepatic carcinogenesis [J].
Cao, J ;
Xu, Y ;
Chen, JS ;
Klaunig, JE .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1996, 29 (02) :244-250
[6]  
Chen LS, 1997, DRUG METAB DISPOS, V25, P1045
[7]   Degradation of green tea catechins in tea drinks [J].
Chen, ZY ;
Zhu, QY ;
Tsang, D ;
Huang, Y .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (01) :477-482
[8]   Stabilizing effect of ascorbic acid on green tea catechins [J].
Chen, ZY ;
Zhu, QY ;
Wong, YF ;
Zhang, ZS ;
Chung, HY .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1998, 46 (07) :2512-2516
[9]   Effect of green tea and black tea on the metabolisms of mineral elements in old rats [J].
Deng, ZY ;
Tao, BY ;
Li, XL ;
He, JM ;
Chen, YF .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1998, 65 (01) :75-86
[10]   Catechin is metabolized by both the small intestine and liver of rats [J].
Donovan, JL ;
Crespy, V ;
Manach, C ;
Morand, C ;
Besson, C ;
Scalbert, A ;
Rémésy, C .
JOURNAL OF NUTRITION, 2001, 131 (06) :1753-1757