Gendron Louis, Mittal Nitish, Beaudry Hélène, Walwyn Wendy
Département de physiologie et biophysique, Institut de pharmacologie de Sherbrooke, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Br J Pharmacol. 2015 Jan;172(2):403-19. doi: 10.1111/bph.12706. Epub 2014 Jul 1.
Within the opioid family of receptors, δ (DOPrs) and μ opioid receptors (MOPrs) are typical GPCRs that activate canonical second-messenger signalling cascades to influence diverse cellular functions in neuronal and non-neuronal cell types. These receptors activate well-known pathways to influence ion channel function and pathways such as the map kinase cascade, AC and PI3K. In addition new information regarding opioid receptor-interacting proteins, downstream signalling pathways and resultant functional effects has recently come to light. In this review, we will examine these novel findings focusing on the DOPr and, in doing so, will contrast and compare DOPrs with MOPrs in terms of differences and similarities in function, signalling pathways, distribution and interactions. We will also discuss and clarify issues that have recently surfaced regarding the expression and function of DOPrs in different cell types and analgesia.
This article is part of a themed section on Opioids: New Pathways to Functional Selectivity. To view the other articles in this section visit http://dx.doi.org/10.1111/bph.2015.172.issue-2.
在阿片受体家族中,δ(DOPrs)和μ阿片受体(MOPrs)是典型的G蛋白偶联受体(GPCRs),它们激活经典的第二信使信号级联反应,以影响神经元和非神经元细胞类型中的多种细胞功能。这些受体激活众所周知的途径来影响离子通道功能以及诸如丝裂原活化蛋白激酶(MAP)激酶级联反应、腺苷酸环化酶(AC)和磷脂酰肌醇-3激酶(PI3K)等途径。此外,关于阿片受体相互作用蛋白、下游信号通路及由此产生的功能效应的新信息最近也已被发现。在本综述中,我们将研究这些新发现,重点关注DOPr,并在此过程中,就功能、信号通路、分布和相互作用方面的异同,将DOPr与MOPr进行对比和比较。我们还将讨论并阐明最近出现的关于DOPr在不同细胞类型中的表达和功能以及镇痛作用的问题。
本文是关于阿片类药物:功能选择性新途径的主题部分的一部分。要查看本部分的其他文章,请访问http://dx.doi.org/10.1111/bph.2015.172.issue-2 。