Biotransformation of green tea polyphenols and the biological activities of those metabolites

被引:194
作者
Lambert, Joshua D. [1 ]
Sang, Shengmin [1 ]
Yang, Chung S. [1 ]
机构
[1] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Biol Chem, Piscataway, NJ 08854 USA
关键词
green tea; catechins; epigallocatechin-3-gallate; biotransformation;
D O I
10.1021/mp700075m
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Green tea (Camellia sinensis, Theaceae) and its major polyphenol constituents, the catechins, have been reported to have many health benefits including the prevention of cancer and heart disease. Many mechanisms of action have been proposed based on in vitro models; however, the importance of most of these mechanisms remains to be determined in vivo. The bioavailability and biotransformation of tea catechins play a key role in determining the importance of various mechanisms in vivo. Likewise, the biological activity and bioavailability of tea catechin metabolites, an understudied area,are important in understanding the potential beneficial effects of tea. In this article, we review the data available on the biotransformation of the tea catechins and the limited data set available on the biological activities of the catechin metabolites. Careful interpretation of available data, carefully designed animal experiments, and integration of bioavailability and biological activity data are needed if the disease preventive activity of tea is to be understood. We hope this article will spark research efforts on some of the important questions regarding tea polyphenol bioavailability, biotransformation, and the biological activities of tea catechin metabolites.
引用
收藏
页码:819 / 825
页数:7
相关论文
共 51 条
  • [1] Glutathione and N-acetylcysteine conjugates of α-methyldopamine produce serotonergic neurotoxicity:: Possible role in methylenedioxyamphetamine-mediated neurotoxicity
    Bai, FJ
    Lau, SS
    Monks, TJ
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1999, 12 (12) : 1150 - 1157
  • [2] The chemistry of tea flavonoids
    Balentine, DA
    Wiseman, SA
    Bouwens, LCM
    [J]. CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) : 693 - 704
  • [3] Chemosensitization of pancreatic cancer by inhibition of the 26S proteasome
    Bold, RJ
    Virudachalam, S
    McConkey, DJ
    [J]. JOURNAL OF SURGICAL RESEARCH, 2001, 100 (01) : 11 - 17
  • [4] Inhibition of human liver catechol-O-methyltransferase by tea catechins and their metabolites:: Structure-activity relationship and molecular-modeling studies
    Chen, D
    Wang, CY
    Lambert, JD
    Ai, N
    Welsh, WJ
    Yang, CS
    [J]. BIOCHEMICAL PHARMACOLOGY, 2005, 69 (10) : 1523 - 1531
  • [5] Chen LS, 1997, DRUG METAB DISPOS, V25, P1045
  • [6] Chow HHS, 2003, CLIN CANCER RES, V9, P3312
  • [7] Chow HHS, 2001, CANCER EPIDEM BIOMAR, V10, P53
  • [8] Daniel KG, 2006, INT J MOL MED, V18, P625
  • [9] Green tea extract and (-)-epigallocatechin-3-gallate, the major tea catechin, exert oxidant but lack antioxidant activities
    Elbling, L
    Weiss, RM
    Teufelhofer, O
    Uhl, M
    Knasmueller, S
    Schulte-Hermann, R
    Berger, W
    Mickshe, M
    [J]. FASEB JOURNAL, 2005, 19 (02) : 807 - +
  • [10] Phytoestrogens are potent inhibitors of estrogen sulfation: Implications for breast cancer risk and treatment
    Harris, RM
    Wood, DM
    Bottomley, L
    Blagg, S
    Owen, K
    Hughes, PJ
    Waring, RH
    Kirk, CJ
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (04) : 1779 - 1787