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吗啡和氟哌啶醇治疗后大鼠肝脏中的N-脱甲基酶活性。

N-demethylase activity in the rat liver following morphine and haloperidol treatment.

作者信息

Daniel W, Melzacka M

出版信息

Pol J Pharmacol Pharm. 1986 Mar-Apr;38(2):199-205.

PMID:3748892
Abstract

A study of the liver N-demethylase activity in rats treated with different dosage schedule of morphine, or with a single dose of haloperidol was carried out. It was found that prolonged administration of morphine to rats inhibited the rate of ethylmorphine demethylation in vitro and diminished the liver cytochrome P450 level. Therefore, it could be assumed that the changes in N-demethylase activity did not play a substantial role in altering of morphine pharmacokinetics. Haloperidol, when given to rats, did not change the microsomal N-demethylase activity in vitro; however, when introduced into incubation mixture, it inhibited the rate of ethylmorphine dealkylation. This indicated that elevation of morphine level in rats by haloperidol was more likely due to a competitive mechanism.

摘要

开展了一项关于用不同剂量方案的吗啡或单剂量氟哌啶醇处理的大鼠肝脏N-脱甲基酶活性的研究。结果发现,对大鼠长期给予吗啡会抑制体外N-脱甲基酶活性并降低肝脏细胞色素P450水平。因此,可以推测N-脱甲基酶活性的变化在改变吗啡药代动力学方面并未发挥重要作用。给大鼠服用氟哌啶醇时,体外微粒体N-脱甲基酶活性未发生变化;然而,当将其引入孵育混合物中时,它会抑制N-脱甲基酶的活性。这表明氟哌啶醇使大鼠体内吗啡水平升高更可能是由于竞争机制。

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