Borowsky S A, Lieber C S
J Pharmacol Exp Ther. 1978 Oct;207(1):123-9.
To determine whether there might be a physiologic basis for the abuse of ethanol by methadone maintenance patients, studies of methadone metabolism were conducted in vivo and in vitro after acute and chronic ethanol administration to rats. Acute administration of ethanol resulted in increased brain and liver concentrations of methadone at two time periods and decreased biliary output of pharmacologically active methadone measured by radioactive tracer technique with [3H]methadone. In vitro, ethanol inhibited N-demethylation of methadone by microsomes from livers of naive rats, with a Ki averaging 32 mM (146 mg/kl). Also, methadone metabolism was inhibited by carbon monoxide indicating cytochrome P-450 dependence as is the case for ethanol. Chronic administration of ethanol to rats led to decreased levels of unmetabolized methadone in brain and liver, in vivo, and to increased microsomal N-demethylation of methadone, in vitro, compared to pair-fed controls. Therefore, acute ethanol administration may enhance cerebral effects of methadone by interfering with degradation of methadone at liver microsomal sites. Chronic ethanol administration increases methadone metabolism by stimulating degradation in liver microsomes.
为了确定美沙酮维持治疗患者滥用乙醇是否可能存在生理基础,在给大鼠急性和慢性给予乙醇后,进行了体内和体外美沙酮代谢研究。急性给予乙醇导致在两个时间段美沙酮在脑和肝脏中的浓度增加,并且通过用[3H]美沙酮的放射性示踪技术测量的具有药理活性的美沙酮胆汁排出量减少。在体外,乙醇抑制来自未接触过乙醇大鼠肝脏的微粒体对美沙酮的N-去甲基化,其Ki平均为32 mM(146 mg/kl)。此外,美沙酮代谢受到一氧化碳抑制,表明与乙醇情况一样,美沙酮代谢依赖细胞色素P-450。与配对喂养的对照相比,对大鼠慢性给予乙醇导致体内脑和肝脏中未代谢美沙酮水平降低,以及体外美沙酮微粒体N-去甲基化增加。因此,急性给予乙醇可能通过干扰肝脏微粒体部位美沙酮的降解来增强美沙酮的脑效应。慢性给予乙醇通过刺激肝脏微粒体中的降解增加美沙酮代谢。