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戊巴比妥、苯妥英和地高辛与乙醇在离体灌注豚鼠肝脏中的相互作用。

Interaction of pentobarbital, diphenylhydantoin and digitoxin with ethanol in the isolated perfused guinea-pig liver.

作者信息

Haacke H, Johnsen K, Kolenda K D

出版信息

Arzneimittelforschung. 1976;26(5):835-9.

PMID:989355
Abstract

In the isolated guinea-pig liver the interactions of ethanol with the metabolism of three drugs (14C-pentobarbital, 14C-diphenylhydantoin, and 2H-digitoxin) has been investigated. The disappearance of ethanol could be described by zero-order kinetics and was not influenced by the three drugs. In the case of 14C-pentobarbital and 14C-diphenylhydantoin after a short period of distribution disappearance of radioactivity was faster under the influence of ethanol, whereas radioactivity in liver tissue was increased. The radioactivity accumulated in the liver tissue predominantly represented the unchanged drugs suggesting that the inhibition of drug metabolism by ethanol was the cause of the altered distribution. In the case of 3H-digitoxin ethanol did neither significantly influence the distribution of radioactivity nor the pronounced biliary excretion. However there exists some evidence for a minor inhibition of 3H-digitoxin's metabolism by ethanol.

摘要

在离体豚鼠肝脏中,研究了乙醇与三种药物(14C-戊巴比妥、14C-苯妥英和3H-洋地黄毒苷)代谢的相互作用。乙醇的消失可用零级动力学描述,且不受这三种药物影响。对于14C-戊巴比妥和14C-苯妥英,在短时间分布后,乙醇影响下放射性的消失更快,而肝组织中的放射性增加。肝组织中积累的放射性主要代表未变化的药物,提示乙醇对药物代谢的抑制是分布改变的原因。对于3H-洋地黄毒苷,乙醇既未显著影响放射性分布,也未显著影响明显的胆汁排泄。然而,有一些证据表明乙醇对3H-洋地黄毒苷的代谢有轻微抑制作用。

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