Induction of UDP-glucuronosyltransferase 1 (UDP-GT1) gene complex by green tea in male F344 rats

被引:41
作者
Embola, CW
Sohn, OS
Fiala, ES
Weisburger, JH
机构
[1] Amer Hlth Fdn, Valhalla, NY 10595 USA
[2] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
关键词
green tea; metabolism; UDP-glucuronosyltransferase (UDP-GT); p-nitrophenol (p-NP); detoxification; microsomes;
D O I
10.1016/S0278-6915(02)00022-4
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Tea is one of the most frequently consumed beverages in the world, second only to water. Epidemiological studies have associated the consumption of green tea with a lower risk of several types of cancers, including stomach, oral cavity, esophagus, and lung. This paper deals with the mechanism of action of tea as an effective chemopreventive agent for toxic chemicals and especially carcinogens. UDP-glueuronosyltransferase (UDP-GT) activities towards p-nitrophenol were markedly increased (51.8% or 1.5-fold) in rats that consumed tea compared with the control animals on water. Induction of UDP-glucuronosyltransferase activity by tea may involve the UDP-GT1 (UGT1A) gene complex of the UDP-GT multigene family. Therefore, a major mechanism of tea as a chemopreventive agent is induction of the microsomal detoxification enzyme, UDP-glucuronosyltransferase. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:841 / 844
页数:4
相关论文
共 18 条
[1]   Functions and transcriptional regulation of PAH-inducible human UDP-glucuronosyltransferases [J].
Bock, KW ;
Gschaidmeier, H ;
Heel, H ;
Lehmköster, T ;
Münzel, PA ;
Bock-Hennig, BS .
DRUG METABOLISM REVIEWS, 1999, 31 (02) :411-422
[2]   AH receptor-controlled transcriptional regulation and function of rat and human UDP-glucuronosyltransferase isoforms [J].
Bock, KW ;
Gschaidmeier, H ;
Heel, H ;
Lehmkoster, T ;
Munzel, PA ;
Raschko, F ;
Bock-Hennig, B .
ADVANCES IN ENZYME REGULATION, VOL 38, 1998, 38 :207-222
[3]   UDP-GLUCURONOSYLTRANSFERASE ACTIVITIES - GUIDELINES FOR CONSISTENT INTERIM TERMINOLOGY AND ASSAY CONDITIONS [J].
BOCK, KW ;
BURCHELL, B ;
DUTTON, GJ ;
HANNINEN, O ;
MULDER, GJ ;
OWENS, IS ;
SIEST, G ;
TEPHLY, TR .
BIOCHEMICAL PHARMACOLOGY, 1983, 32 (06) :953-955
[4]   In situ hybridization studies of UDP-glucuronosyltransferase UGT1A6 expression in rat testis and brain [J].
Brands, A ;
Münzel, PA ;
Bock, KW .
BIOCHEMICAL PHARMACOLOGY, 2000, 59 (11) :1441-1444
[5]   UDP-glucuronyl transferase enzyme family in both human and balb/c mouse lung [J].
Conner, CE ;
Burchell, B ;
Hume, R .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1997, 25 (02) :S181-S181
[6]   EFFECTS OF PHENETHYL ISOTHIOCYANATE, A CARCINOGENESIS INHIBITOR, ON XENOBIOTIC-METABOLIZING ENZYMES AND NITROSAMINE METABOLISM IN RATS [J].
GUO, ZY ;
SMITH, TJ ;
WANG, E ;
SADRIEH, N ;
MA, Q ;
THOMAS, PE ;
YANG, CS .
CARCINOGENESIS, 1992, 13 (12) :2205-2210
[7]  
ISSELBACHER KJ, 1962, J BIOL CHEM, V237, P3033
[8]   IMMUNOCHEMICAL AND FUNCTIONAL-CHARACTERIZATION OF UDP-GLUCURONOSYLTRANSFERASES FROM RAT-LIVER, INTESTINE AND KIDNEY [J].
KOSTER, AS ;
SCHIRMER, G ;
BOCK, KW .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (22) :3971-3975
[9]   Cancer chemoprevention by tea polyphenols through mitotic signal transduction blockade [J].
Lin, JK ;
Liang, YC ;
Lin-Shiau, SY .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (06) :911-915
[10]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265