Phillips I R, Shephard E A, Mitani F, Rabin B R
Biochem J. 1981 Jun 15;196(3):839-51. doi: 10.1042/bj1960839.
The treatment of rats for 4 days with phenobarbital causes an apparent 3-fold increase in the amount of total liver cytochrome P-450. By sodium dodecyl sulphate/polyacrylamide-gel electrophoresis, metyrapone binding and immunoprecipitation, this increase was found to be due to a much larger increase in a restricted number of specific cytochrome P-450 variants. A radioimmunoassay technique demonstrated that the major phenobarbital-inducible variant, of molecular weight 52 000, is induced 24-fold by phenobarbital. Immunoprecipitation analysis of products of translation in vitro with an antibody specific to the 52 000-mol.wt. cytochrome P-450 showed that phenobarbital induces the mRNA in polyribosomes for this variant 20-fold. Evidence is presented for the action of phenobarbital at the transcriptional and translational levels.
用苯巴比妥对大鼠进行为期4天的处理,可使肝脏中细胞色素P - 450的总量明显增加3倍。通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳、甲吡酮结合及免疫沉淀分析发现,这种增加是由于特定数量有限的细胞色素P - 450变体大幅增加所致。放射免疫测定技术表明,分子量为52000的主要苯巴比妥诱导变体被苯巴比妥诱导了24倍。用针对分子量为52000的细胞色素P - 450的特异性抗体对体外翻译产物进行免疫沉淀分析表明,苯巴比妥可使该变体在多核糖体中的mRNA诱导增加20倍。本文提供了苯巴比妥在转录和翻译水平上发挥作用的证据。