Phenobarbital induction of drug/steroid-metabolizing enzymes and nuclear receptor CAR

被引:55
作者
Kakizaki, S [1 ]
Yamamoto, Y [1 ]
Ueda, A [1 ]
Moore, R [1 ]
Sueyoshi, T [1 ]
Negishi, M [1 ]
机构
[1] NIEHS, Pharmacogenet Sect, Reprod & Dev Toxicol Lab, NIH, Res Triangle Pk, NC 27709 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2003年 / 1619卷 / 03期
关键词
metabolizing enzyme; nuclear receptor; phenobarbital;
D O I
10.1016/S0304-4165(02)00482-8
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
Phenobarbital (PB) increases hepatic drug/steroid-metabolic capability by coordinately activating transcription of the genes encoding various metabolizing enzymes. The nuclear receptor CAR was first implicated as a transcription factor that activates the cytochrome P450 Cyp2b10 gene. In response to PB, CAR forms a heterodimer with the retinoid X receptor (RXR), binds to a PB response element (typified by DR-4 motif), and activates transcription of the gene. In the CAR-null mouse, PB does not only induce the Cyp2b10 gene, but also induces genes encoding various metabolizing enzymes. Thus, CAR is a general nuclear receptor that is essential for PB induction of drug/steroid metabolizing enzymes. PB also induces amino levulinate synthase 1 (ALAS-1), the rate-limiting enzyme in heme biosynthesis, to increase heme supply. However, PB induction of the synthase occurs in CAR-null mice, suggesting that CAR does not coordinate the heme synthesis for the induction of drug/steroid metabolism. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:239 / 242
页数:4
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