Satoh T, Sugiyama S, Kitagawa H
Res Commun Chem Pathol Pharmacol. 1979 Dec;26(3):547-62.
The higher inhibition of liver microsomal carboxylesterase (CEase) by EPN, as compared to that of acetylcholinesterase (AchE) may be, at least in part, explained by the present findings that NAD potentiated the anti-CEase, but not anti-AchE, action of EPN. This phenomenon was referred to as "NAD-effect" in this paper. NAD-effect was not due to the increased formation of oxygen analog of EPN (EPN=O) by NAD addition through liver microsomal cytochrome P-450 catalyzed monoxygenase, because the amounts of EPN=O formed during incubation in the presence and absence of NAD were not significantly changed as shown by gaschromatography-mass spectrometric estimations. In addition, HAD-effect could be observed in the experiments even under carbon monoxide atmosphere. Such NAD-effect was observed only when NAD, EPN and an unidentified component bound to liver microsomal membrane were co-existent in the incubation mixture.
与乙酰胆碱酯酶(AchE)相比,EPN对肝脏微粒体羧酸酯酶(CEase)的抑制作用更强,这至少部分可以由本研究结果解释,即NAD增强了EPN的抗CEase作用,但未增强其抗AchE作用。本文将这种现象称为“NAD效应”。NAD效应并非由于通过肝脏微粒体细胞色素P-450催化的单加氧酶添加NAD而增加了EPN的氧类似物(EPN=O)的形成,因为气相色谱-质谱估计显示,在有和没有NAD的情况下孵育期间形成的EPN=O的量没有显著变化。此外,即使在一氧化碳气氛下的实验中也能观察到HAD效应。只有当NAD、EPN和与肝脏微粒体膜结合的一种未鉴定成分同时存在于孵育混合物中时,才会观察到这种NAD效应。