Suppression of the expression of the CYP2B1/2 gene by retinoic acids

被引:10
作者
Yamada, H [1 ]
Yamaguchi, T [1 ]
Oguri, K [1 ]
机构
[1] Kyushu Univ, Grad Sch Pharmaceut Sci, Higashi Ku, Fukuoka 8128582, Japan
关键词
CYP2B1; CYP2B2; phenobarbital; retinoic acid; constitutive androstane receptor; retinoid X-receptor;
D O I
10.1006/bbrc.2000.3620
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
The effects of 5 alpha -androsten-3 alpha -ol (ASE), and retinoic acids (RAs) and their precursors on the phenobarbital (PB)-mediated induction of CYP2B1 and 2B2 were examined in cultured rat hepatocytes. Two isomers of RA, 9-cis- and all-trans-RA, suppressed markedly the effect of PB on CYP2B1/2 expression, while ASE had no suppressive effect. The effect of 9-cis-RA appeared at a lower concentration than the all-trans-isomer, indicating the dominant action of the former isomer. Suppression with 9-cis-retinal was also observed, but all-trans-retinol and -retinal were without effect. These results suggest that: (1) ASE, an inverse agonist for the constitutive androstane receptor (CAR), does not play a major role in the suppression of the CYP2B; (2) 9-cis-RA suppresses CYP2B induction by reducing ligand-free retinoid X-receptors (RXR) available for dimerization with the CAR; and (3) enzymes responsible for RA formation play an important role in the mechanism governing CYP2B regulation. (C) 2000 Academic Press.
引用
收藏
页码:66 / 71
页数:6
相关论文
共 41 条
[1]  
Auwerx J, 1999, CELL, V97, P161
[2]   A TIME-COURSE INVESTIGATION OF VITAMIN-A LEVELS AND DRUG-METABOLIZING ENZYME-ACTIVITIES IN RATS FOLLOWING A SINGLE TREATMENT WITH PROTOTYPIC POLYCHLORINATED-BIPHENYLS AND DDT [J].
AZAIS, V ;
ARAND, M ;
RAUCH, P ;
SCHRAMM, H ;
BELLENAND, P ;
NARBONNE, JF ;
OESCH, F ;
PASCAL, G ;
ROBERTSON, LW .
TOXICOLOGY, 1987, 44 (03) :341-354
[3]   A NEW ORPHAN MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY THAT INTERACTS WITH A SUBSET OF RETINOIC ACID RESPONSE ELEMENTS [J].
BAES, M ;
GULICK, T ;
CHOI, HS ;
MARTINOLI, MG ;
SIMHA, D ;
MOORE, DD .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1544-1552
[4]   RETINOIC ACID REGULATES GROWTH-HORMONE GENE-EXPRESSION [J].
BEDO, G ;
SANTISTEBAN, P ;
ARANDA, A .
NATURE, 1989, 339 (6221) :231-234
[5]   A RAPID, SENSITIVE METHOD FOR DETECTION OF ALKALINE-PHOSPHATASE CONJUGATED ANTI-ANTIBODY ON WESTERN BLOTS [J].
BLAKE, MS ;
JOHNSTON, KH ;
RUSSELLJONES, GJ ;
GOTSCHLICH, EC .
ANALYTICAL BIOCHEMISTRY, 1984, 136 (01) :175-179
[6]   Differential transactivation by two isoforms of the orphan nuclear hormone receptor CAR [J].
Choi, HS ;
Chung, MR ;
Tzameli, I ;
Simha, D ;
Lee, YK ;
Seol, W ;
Moore, DD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (38) :23565-23571
[7]   UPTAKE AND CELLULAR-TRANSPORT OF [11-H-3] ALL-TRANS-RETINOIC ACID IN THE LIVER OF VITAMIN-A-DEFICIENT HAMSTERS [J].
CHOWDHURY, A ;
CHOPRA, DP .
TISSUE & CELL, 1988, 20 (04) :555-565
[9]   Androstane metabolites bind to and deactivate the nuclear receptor CAR-β [J].
Forman, BM ;
Tzameli, I ;
Choi, HS ;
Chen, L ;
Simha, D ;
Seol, W ;
Evans, RM ;
Moore, DD .
NATURE, 1998, 395 (6702) :612-615
[10]   Characterization of a phenobarbital-responsive enhancer module in mouse P450 Cyp2b10 gene [J].
Honkakoski, P ;
Negishi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (23) :14943-14949