Zakharova N E, Mordvinov V A, Tsyrlov I B, Liakhovich V V
Biull Eksp Biol Med. 1976;81(4):418-20.
The dependence of expressiveness of microsomal mono-oxygenase induction by phenobarbital upon the amount of binding sites at cytochrome P-450 active center(s) has been studied. The experimental cholestasis is accompanied by accumulation of hydroxylated derivatives of cholesterol, which possess the detergent characteristics and destruct the substrate binding sites in P-450 molecule. The possibility has been demonstrated of phenobarbital induction under conditions when the inducer-monooxygenase primary binding and metabolic steps are not involved. It is assumed that the activation of de novo microsomal protein synthesis is effected by the molecule of phenobarbital itself and not by the products of its primary hydroxylation in the microsomes.
研究了苯巴比妥对微粒体单加氧酶诱导表达的作用,其依赖于细胞色素P - 450活性中心结合位点的数量。实验性胆汁淤积伴随着胆固醇羟基化衍生物的积累,这些衍生物具有去污剂特性,会破坏P - 450分子中的底物结合位点。已证明在不涉及诱导剂 - 单加氧酶初级结合和代谢步骤的条件下,苯巴比妥仍可诱导。推测微粒体蛋白从头合成的激活是由苯巴比妥分子本身实现的,而非其在微粒体中初级羟基化的产物。