Molecular pharmacology of the opioid receptors

被引:190
作者
Satoh, M
Minami, M
机构
[1] Department of Molecular Pharmacology, Faculty of Pharmaceutical Sciences, Kyoto University, Kyoto
关键词
opioid receptors; molecular cloning; receptor subtypes; second messenger systems; in situ hybridization; morphine;
D O I
10.1016/0163-7258(95)02011-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 x, 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.
引用
收藏
页码:343 / 364
页数:22
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