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阿片受体的分子药理学

Molecular pharmacology of the opioid receptors.

作者信息

Satoh M, Minami M

机构信息

Department of Molecular Pharmacology, Kyoto University, Japan.

出版信息

Pharmacol Ther. 1995;68(3):343-64. doi: 10.1016/0163-7258(95)02011-x.

Abstract

Opioid receptors are the primary sites of actions of opiates and endogenous opioid peptides, which have a wide variety of pharmacological and physiological effects. The opioid receptors are classified into at least three subtypes, mu, delta, and kappa, and their cDNAs have been cloned. In this review, we describe the molecular cloning of opioid receptor gene family and studies of the structure-function relationships, modes of coupling to second messenger systems, pharmacological effects of antisense oligonucleotides, and anatomical distribution of opioid receptor mRNAs.

摘要

阿片受体是阿片类药物和内源性阿片肽的主要作用位点,它们具有广泛的药理和生理效应。阿片受体至少可分为三种亚型,即μ、δ和κ亚型,其cDNA已被克隆。在本综述中,我们描述了阿片受体基因家族的分子克隆以及结构-功能关系、与第二信使系统的偶联方式、反义寡核苷酸的药理作用和阿片受体mRNA的解剖分布的研究。

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