Aida K, Negishi M
Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709.
Biochemistry. 1991 Aug 13;30(32):8041-5. doi: 10.1021/bi00246a023.
The induction mechanism by pyrazole or phenobarbital of coumarin 7-hydroxylase (cytochrome P450coh) was investigated in DBA/2J male mice. The P450coh mRNA in the pyrazole-induced mice was increased gradually to a 20-fold higher level within 48 h, yet transcription of the P450coh gene was not affected. The half-life of P450coh mRNA, on the other hand, was at least 4-fold longer in the pyrazole-induced DBA/2J (approximately 6.0 h) than in control DBA/2J (approximately 1.5 h) male mice. The stabilization of P450coh mRNA, therefore, is the primary mechanism for the induction by pyrazole of coumarin 7-hydroxylase. Phenobarbital, on the other hand, regulates the induction either translationally or posttranslationally. This drug affected neither the P450coh mRNA nor the P450coh gene's transcription levels in the DBA/2J male mice, although Western blots showed approximately a 3-fold increase of the P450coh protein in the liver microsomes of the drug-treated mice. The results indicate, therefore, that both phenobarbital and pyrazole regulate the P450coh induction posttranscriptionally; the former inducer enhances the translational efficiency of P450coh mRNA or alters the degradation rate of P450coh aproprotein, while the latter stabilizes P450coh mRNA.
在DBA/2J雄性小鼠中研究了吡唑或苯巴比妥对香豆素7-羟化酶(细胞色素P450coh)的诱导机制。吡唑诱导的小鼠中,P450coh mRNA在48小时内逐渐增加至高出20倍的水平,但P450coh基因的转录未受影响。另一方面,吡唑诱导的DBA/2J雄性小鼠中P450coh mRNA的半衰期(约6.0小时)比对照DBA/2J雄性小鼠(约1.5小时)至少长4倍。因此,P450coh mRNA的稳定化是吡唑诱导香豆素7-羟化酶的主要机制。另一方面,苯巴比妥通过翻译或翻译后水平调节诱导作用。该药物对DBA/2J雄性小鼠的P450coh mRNA和P450coh基因转录水平均无影响,尽管蛋白质免疫印迹显示药物处理小鼠肝微粒体中P450coh蛋白增加了约3倍。因此,结果表明苯巴比妥和吡唑均在转录后调节P450coh的诱导;前者诱导剂提高P450coh mRNA的翻译效率或改变P450coh前体蛋白的降解速率,而后者使P450coh mRNA稳定。