Minami M, Satoh M
Department of Molecular Pharmacology, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.
Neurosci Res. 1995 Sep;23(2):121-45. doi: 10.1016/0168-0102(95)00933-k.
Opiates like morphine and endogenous opioid peptides exert their pharmacological and physiological effects through binding to their endogenous receptors, opioid receptors. The opioid receptors are classified into at least three types, mu-, delta- and kappa-types. Recently, cDNAs of the opioid receptors have been cloned and have greatly advanced our understanding of their structure, function and expression. This review focuses on the recent advances in the studies on opioid receptors using the cloned cDNAs. We describe the molecular cloning of the opioid receptor gene family and studies of the structure-function relationships, modes of coupling to second messenger systems, pharmacological effects of antisense oligonucleotide and anatomical distributions of opioid receptors.
吗啡等阿片类药物和内源性阿片肽通过与内源性受体——阿片受体结合来发挥其药理和生理作用。阿片受体至少可分为三种类型,即μ型、δ型和κ型。最近,阿片受体的cDNA已被克隆出来,这极大地推动了我们对其结构、功能和表达的认识。本综述着重介绍利用克隆的cDNA对阿片受体进行研究所取得的最新进展。我们将描述阿片受体基因家族的分子克隆、结构-功能关系研究、与第二信使系统的偶联方式、反义寡核苷酸的药理作用以及阿片受体的解剖分布。