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综述文章:H2受体拮抗剂与乙醇相互作用缺乏临床意义

Review article: lack of clinical significance of the interaction between H2-receptor antagonists and ethanol.

作者信息

Levitt M D

机构信息

Minneapolis Veterans Administration Medical Center, MN 55417.

出版信息

Aliment Pharmacol Ther. 1993 Apr;7(2):131-8. doi: 10.1111/j.1365-2036.1993.tb00081.x.

DOI:10.1111/j.1365-2036.1993.tb00081.x
PMID:8097933
Abstract

It has been proposed that an appreciable fraction of ingested ethanol is metabolized in the gastric mucosa and that inhibition of this metabolism by H2-receptor antagonists produces clinically important increases in blood ethanol. This paper reviews available data concerning gastric metabolism of ethanol and the influence of H2-antagonists on ethanol metabolism. It concludes that very little, if any, metabolism of ethanol is likely to occur in the gastric mucosa, and the interaction between H2-antagonists and ethanol is clinically insignificant.

摘要

有人提出,摄入的乙醇有相当一部分在胃黏膜中代谢,并且H2受体拮抗剂对这种代谢的抑制会导致血液中乙醇含量出现具有临床意义的升高。本文综述了关于乙醇胃代谢以及H2拮抗剂对乙醇代谢影响的现有数据。结论是,乙醇在胃黏膜中的代谢即使有也微乎其微,并且H2拮抗剂与乙醇之间的相互作用在临床上无足轻重。

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Review article: lack of clinical significance of the interaction between H2-receptor antagonists and ethanol.综述文章:H2受体拮抗剂与乙醇相互作用缺乏临床意义
Aliment Pharmacol Ther. 1993 Apr;7(2):131-8. doi: 10.1111/j.1365-2036.1993.tb00081.x.
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H2-antagonists and alcohol. Do they interact?H2拮抗剂与酒精。它们会相互作用吗?
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Bioavailability of alcohol: role of gastric metabolism and its interaction with other drugs.酒精的生物利用度:胃代谢的作用及其与其他药物的相互作用。
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Inhibition of gastric alcohol dehydrogenase activity by histamine H2-receptor antagonists has no influence on the pharmacokinetics of ethanol after a moderate dose.组胺H2受体拮抗剂对胃乙醇脱氢酶活性的抑制作用对中等剂量乙醇的药代动力学没有影响。
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Ethanol and H2-receptor antagonists.
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引用本文的文献

1
Pharmacokinetic interactions between alcohol and other drugs.酒精与其他药物之间的药代动力学相互作用。
Clin Pharmacokinet. 1997 Aug;33(2):79-90. doi: 10.2165/00003088-199733020-00001.
2
Inter-individual and intra-individual variability of ethanol concentration-time profiles: comparison of ethanol ingestion before or after an evening meal.乙醇浓度-时间曲线的个体间和个体内变异性:晚餐前后乙醇摄入量的比较。
Br J Clin Pharmacol. 1995 Oct;40(4):387-92. doi: 10.1111/j.1365-2125.1995.tb04561.x.
3
Lack of effect of H2-receptor antagonists on the pharmacokinetics of alcohol consumed after food at lunchtime.
午餐进食后服用H2受体拮抗剂对酒精药代动力学无影响。
Br J Clin Pharmacol. 1994 Apr;37(4):371-4. doi: 10.1111/j.1365-2125.1994.tb04291.x.
4
H2-antagonists and alcohol. Do they interact?H2拮抗剂与酒精。它们会相互作用吗?
Drug Saf. 1994 Apr;10(4):271-80. doi: 10.2165/00002018-199410040-00001.
5
Ranitidine increases the bioavailability of postprandial ethanol by the reduction of first pass metabolism.雷尼替丁通过减少首过代谢来提高餐后乙醇的生物利用度。
Gut. 1995 Sep;37(3):413-7. doi: 10.1136/gut.37.3.413.
6
First-pass metabolism of alcohol. Absence of diurnal variation and its inhibition by cimetidine after evening meal.酒精的首过代谢。晚餐后无昼夜变化及其被西咪替丁抑制的情况。
Dig Dis Sci. 1995 Oct;40(10):2091-7. doi: 10.1007/BF02208989.