Matsubara T, Touchi A
Jpn J Pharmacol. 1977 Oct;27(5):701-8. doi: 10.1254/jjp.27.701.
Cyanide, an inhibitor of many hemoproteins, was shown to affect a number of microsomal drug-metabolizing activities catalyzed by cytochrome P-450. The N-demethylation reaction of aminopyrine was inhibited noncompetitively by this inhibitor in microsomal preparations from rats. The binding reaction of aminopyrine with microsomal cytochrome P-450 was also modified by cyanide, and an abnormal aminopyrine-induced difference spectrum of microsomes by cyanide, and an abnormal aminopyrine-induced difference spectrum of microsomes appeared when cyanide was added to the reaction mixture. Partial dissociation of cytochrome P-450. Cyanide complex by aminopyrine was observed by spectrophotometrical and epr spectroscopic methods. These results suggest that aminopyrine and cyanide reciprocally affect binding with cytochrome P-450 and modification by cyanide of aminopyrine binding reaction with the hemoprotein produces an inhibition of N-demethylase activity.
氰化物是许多血红蛋白的抑制剂,已证明它会影响细胞色素P - 450催化的多种微粒体药物代谢活性。在大鼠微粒体制剂中,该抑制剂对氨基比林的N - 去甲基化反应具有非竞争性抑制作用。氰化物还改变了氨基比林与微粒体细胞色素P - 450的结合反应,当向反应混合物中加入氰化物时,会出现异常的氨基比林诱导的微粒体差异光谱。观察到细胞色素P - 450。通过分光光度法和电子顺磁共振光谱法观察到氨基比林对氰化物复合物的部分解离。这些结果表明,氨基比林和氰化物相互影响与细胞色素P - 450的结合,并且氰化物对氨基比林与血红蛋白结合反应的修饰会导致N - 脱甲基酶活性受到抑制。