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西咪替丁对微粒体单加氧酶的抑制性质。

The nature of microsomal monooxygenase inhibition by cimetidine.

作者信息

Winzor D J, Ioannoni B, Reilly P E

出版信息

Biochem Pharmacol. 1986 Jul 1;35(13):2157-61. doi: 10.1016/0006-2952(86)90586-1.

Abstract

A kinetic investigation of the inhibitory effect of cimetidine on the O-dealkylation of 7-ethoxyresorufin by rat liver microsomes has yielded linear Lineweaver-Burk plots which intersect in the second quadrant. Though technically compatible with non-competitive inhibition, the results are shown to be readily explained by the more realistic molecular concept of competitive inhibition by invoking the involvement of cytochrome P-450 isoenzymes with widely different KI values. Microsomal monooxygenase heterogeneity is also shown to provide a plausible explanation of other published results signifying the departure of chloramphenicol and phenacetin from the concept of competitive inhibition despite competition with substrate for the active-site haem group of cytochrome P-450.

摘要

对西咪替丁抑制大鼠肝微粒体使7-乙氧基试卤灵O-脱烷基化作用进行的动力学研究得出了在第二象限相交的线性Lineweaver-Burk图。虽然从技术上看与非竞争性抑制相符,但通过援引具有广泛不同KI值的细胞色素P-450同工酶的参与,这些结果表明用更实际的竞争性抑制分子概念能很容易地解释。微粒体单加氧酶的异质性也为其他已发表结果提供了一个合理的解释,这些结果表明氯霉素和非那西丁不符合竞争性抑制概念,尽管它们与底物竞争细胞色素P-450活性位点的血红素基团。

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