Green tea as inhibitor of the intestinal absorption of lipids: potential mechanism for its lipid-lowering effect

被引:303
作者
Koo, Sung I. [1 ]
Noh, Sang K.
机构
[1] Univ Connecticut, Dept Nutrit Sci, Storrs, CT 06269 USA
[2] Changwon Natl Univ, Dept Food & Nutr, Kyongnam 641773, South Korea
关键词
intestinal absorption; lipids; green tea; (-)-epigallocatechin gallate;
D O I
10.1016/j.jnutbio.2006.12.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Animal and epidemiological studies suggest that green tea catechins may reduce the risk of cardiovascular diseases [e.g., coronary heart disease (CHD)]. The health benefit of green tea has been attributed to its antioxidant and anti-inflammatory properties; however, considerable evidence suggests that green tea and its catechins may reduce the risk of CHD by lowering the plasma levels of cholesterol and triglyceride. Although the mechanism underlying such effect of green tea is yet to be determined, it is evident from in vitro and in vivo studies that green tea or catechins inhibit the intestinal absorption of dietary lipids. Studies in vitro indicate that green tea catechins, particularly (-)-epigallocatechin gallate, interfere with the emulsification, digestion, and micellar solubilization of lipids, critical steps involved in the intestinal absorption of dietary fat, cholesterol, and other lipids. Based on the observations, it is likely that green tea or its catechins lower the absorption and tissue accumulation of other lipopbilic organic compounds. The available information strongly suggests that green tea or its catechins may be used as safe and effective lipid-lowering therapeutic agents. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:179 / 183
页数:5
相关论文
共 58 条
[11]   Flavonoids: A class of modulators with bifunctional interactions at vicinal ATP- and steroid-binding sites on mouse P-glycoprotein [J].
Conseil, G ;
Baubichon-Cortay, H ;
Dayan, G ;
Jault, JM ;
Barron, D ;
Di Pietro, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :9831-9836
[12]   Enhancement of antioxidative ability of rat plasma by oral administration of (-)-epicatechin [J].
Da Silva, EL ;
Piskula, M ;
Terao, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (7-8) :1209-1216
[13]  
Guharay J, 2001, PROTEINS, V43, P75, DOI 10.1002/1097-0134(20010501)43:2<75::AID-PROT1019>3.0.CO
[14]  
2-7
[15]  
Harbowy ME, 1997, CRIT REV PLANT SCI, V16, P415, DOI 10.1080/713608154
[16]   Reduced progression of atherosclerosis in apolipoprotein E-deficient mice following consumption of red wine, or its polyphenols quercetin or catechin, is associated with reduced susceptibility of LDL to oxidation and aggregation [J].
Hayek, T ;
Fuhrman, B ;
Vaya, J ;
Rosenblat, M ;
Belinky, P ;
Coleman, R ;
Elis, A ;
Aviram, M .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (11) :2744-2752
[17]   DIETARY ANTIOXIDANT FLAVONOIDS AND RISK OF CORONARY HEART-DISEASE - THE ZUTPHEN ELDERLY STUDY [J].
HERTOG, MGL ;
FESKENS, EJM ;
HOLLMAN, PCH ;
KATAN, MB ;
KROMHOUT, D .
LANCET, 1993, 342 (8878) :1007-1011
[18]   Regular ingestion of tea does not inhibit in vivo lipid peroxidation in humans [J].
Hodgson, JM ;
Croft, KD ;
Mori, TA ;
Burke, V ;
Beilin, LJ ;
Puddey, IB .
JOURNAL OF NUTRITION, 2002, 132 (01) :55-58
[19]   Bioavailability of flavonoids from tea [J].
Hollman, PCH ;
Tijburg, LBM ;
Yang, CS .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) :719-738
[20]  
Homan R, 1998, J LIPID RES, V39, P1197