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添加来自6-氨基烟酰胺处理的饥饿大鼠的肝细胞溶胶增强EPN对肝微粒体羧酸酯酶的抑制作用。

Potentiation of EPN-induced inhibition of liver microsomal carboxylesterase by addition of liver cytosol from 6-aminonicotinamide-treated, starved rats.

作者信息

Sugiyama S, Satoh T, Ueno K, Igarashi T, Kitagawa H

出版信息

Jpn J Pharmacol. 1984 Aug;35(4):433-7. doi: 10.1254/jjp.35.433.

Abstract

Addition of liver cytosol from 16 hr-starved rats treated with 6-aminonicotinamide to rat liver microsomes caused potentiation of the anti-carboxylesterase action of ethyl-p-nitrophenyl phenylphosphonothioate (EPN). This was not found when liver cytosol from non-pretreated rats after 16 hr-starvation was used. This potentiation of EPN-induced inhibition of carboxylesterase may be, at least in part, explained by the fact that treatment of rats with 6-aminonicotinamide resulted in a significant increase in NADPH level in liver cytosol which, in turn, stimulated formation of an EPN oxygen analog, a potent inhibitor of carboxylesterase, through cytochrome P-450-coupled monooxygenase.

摘要

将用6-氨基烟酰胺处理过的饥饿16小时大鼠的肝细胞溶胶添加到大鼠肝微粒体中,会增强对氧磷(EPN)的抗羧酸酯酶作用。而使用饥饿16小时后未经预处理大鼠的肝细胞溶胶时,未发现这种情况。EPN诱导的羧酸酯酶抑制作用的这种增强,至少部分可以通过以下事实来解释:用6-氨基烟酰胺处理大鼠会导致肝细胞溶胶中NADPH水平显著增加,进而通过细胞色素P-450偶联单加氧酶刺激形成一种EPN氧类似物,这是一种有效的羧酸酯酶抑制剂。

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