Parola A L, Yamamura H I, Laird H E
Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson 85724.
Life Sci. 1993;52(16):1329-42. doi: 10.1016/0024-3205(93)90168-3.
Since their first description as anomalous high affinity diazepam binding sites in rat peripheral tissues, the peripheral-type benzodiazepine receptor (PBR) has been increasingly studied to better understand nonneural effects of the benzodiazepines. The mammalian PBR is ubiquitously distributed with high concentrations in the outer mitochondrial membrane of secretory tissues. In regions of the brain, the density of PBR can equal or exceed the density of central-type benzodiazepine receptors. High affinity PK 11195 binding is diagnostic for the receptor while the affinity for benzodiazepines is species dependent. Recent cDNA cloning of a PBR component, the isoquinoline binding protein (IBP), shows no apparent sequence homology with any GABAA receptor subunits known to comprise central benzodiazepine receptor subtypes. The PBR seems at best only distantly related to CBRs. Recent advances in the pharmacology, biochemistry and molecular biology of the PBR are reviewed.
自从外周型苯二氮䓬受体(PBR)最初在大鼠外周组织中被描述为异常高亲和力的地西泮结合位点以来,人们对其进行了越来越多的研究,以更好地理解苯二氮䓬类药物的非神经效应。哺乳动物的PBR广泛分布,在分泌组织的线粒体外膜中浓度很高。在脑区,PBR的密度可以等于或超过中枢型苯二氮䓬受体的密度。高亲和力的PK 11195结合是该受体的诊断依据,而对苯二氮䓬类药物的亲和力则因物种而异。最近对PBR的一个组分异喹啉结合蛋白(IBP)进行的cDNA克隆显示,它与已知构成中枢苯二氮䓬受体亚型的任何GABAA受体亚基均无明显的序列同源性。PBR似乎与中枢苯二氮䓬受体(CBRs)至多只有远缘关系。本文综述了PBR在药理学、生物化学和分子生物学方面的最新进展。