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雄性大鼠肝脏微粒体对乙基吗啡的N-去甲基化和O-去乙基化研究。

Studies on the N-demethylation and O-de-ethylation of ethylmorphine by hepatic microsomes from male rats.

作者信息

Thompson J A, Holtzman J L

出版信息

Drug Metab Dispos. 1977 Jan-Feb;5(1):9-14.

PMID:13981
Abstract

On the basis of inhibition studies of the dealkylation of morphine and norcodeine, George and Tephly concluded that O-dealkylation and N-dealkylation are catalyzed by different enzymes. We have examined the microsomal dealkylation of 3-O-[1'-14Clethylmorphine by measuring HCHO colorimetrically and [1-14C]acetaldehyde radiometrically. We find that the KM for the O-de-ethylation is 57 muM, which is quite close to the KS(71 muM) for the type I binding of ethylmorphine in similar preparations. On the other hand, the KM for N-demethylation was 250 muM. Further, the N-demethylation was stoichiometric with the stimulation of both NADPH-cytochrome P-450 reductase and NADPH oxidase, whereas the sum of the N-demethylation and O-de-ethylation was significantly greater, suggesting that the O-de-ethylase activity does not involve stimulation of either of these two activities. Induction with phenobarbital increaesed N-demethylation 118% but did not affect O-de-ethylation. Finally, D2O inhibited the N-demethylase more than the O-de-ethylase.

摘要

基于对吗啡和去甲可待因脱烷基化的抑制研究,乔治和特夫利得出结论,O-脱烷基化和N-脱烷基化由不同的酶催化。我们通过比色法测量甲醛和放射性测量[1-14C]乙醛,研究了3-O-[1'-14C]乙基吗啡的微粒体脱烷基化。我们发现O-去乙基化的KM为57μM,这与类似制剂中乙基吗啡I型结合的KS(71μM)非常接近。另一方面,N-去甲基化的KM为250μM。此外,N-去甲基化与NADPH-细胞色素P-450还原酶和NADPH氧化酶的刺激呈化学计量关系,而N-去甲基化和O-去乙基化的总和明显更大,这表明O-去乙基酶活性不涉及这两种活性中的任何一种的刺激。苯巴比妥诱导使N-去甲基化增加118%,但不影响O-去乙基化。最后,重水对N-去甲基酶的抑制作用比对O-去乙基酶的抑制作用更强。

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