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阿片肽及其受体。

Opioid peptides and their receptors.

作者信息

Kosterlitz H W

出版信息

Prog Biochem Pharmacol. 1980;16:3-10. doi: 10.1016/b978-0-08-028021-9.50005-8.

Abstract

The three agonists, methionine-enkephalin, leucine-enkephalin and beta-endorphin have different pharmacological patterns. It may be of particular importance that they vary in their relative affinities to the enkephalin and naltrexone binding sites in the brain; the former are probably related to delta-receptors prevalent in the mouse vas deferens and the later to mu-receptors prevalent in the guinea-pig. It is possible that mu-receptors are more important for the mediation of analgesic effects than delta-receptors. An understanding of the pharmacokinetics of the opioid peptides will be of basic importance for the design of enkephalin analogues suitable for use as analgesics in man.

摘要

三种激动剂,即甲硫氨酸脑啡肽、亮氨酸脑啡肽和β-内啡肽,具有不同的药理模式。特别重要的是,它们对脑中脑啡肽和纳曲酮结合位点的相对亲和力各不相同;前者可能与小鼠输精管中普遍存在的δ受体有关,而后者与豚鼠中普遍存在的μ受体有关。μ受体可能比δ受体在介导镇痛作用方面更为重要。了解阿片肽的药代动力学对于设计适合人类用作镇痛药的脑啡肽类似物至关重要。

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