μ-Opioid receptor 6-transmembrane isoform: A potential therapeutic target for new effective opioids

被引:19
作者
Convertino, Marino [1 ]
Samoshkin, Alexander [2 ]
Gauthier, Josee [3 ]
Gold, Michael S. [4 ]
Maixner, William [3 ]
Dokholyan, Nikolay V. [1 ]
Diatchenko, Luda [2 ]
机构
[1] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[2] McGill Univ, Alan Edwards Ctr Res Pain, Montreal, PQ H3A 0G1, Canada
[3] Univ N Carolina, Ctr Pain Res & Innovat, KOHSB, Chapel Hill, NC 27599 USA
[4] Univ Pittsburgh, Sch Med, Dept Anesthesiol, Pittsburgh, PA 15213 USA
关键词
6TM MOR isoform; Drug discovery; Review; mu-Opioid receptor; MORPHINE-INDUCED ANALGESIA; TRIGEMINAL NUCLEUS SLICES; MOR-1 SPLICE VARIANTS; G-BETA-GAMMA; INDUCED HYPERALGESIA; SUBSTANCE-P; FUNCTIONAL SELECTIVITY; ADENYLYL-CYCLASE; MICE LACKING; TOLERANCE;
D O I
10.1016/j.pnpbp.2014.11.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The mu-opioid receptor (MOR) is the primary target for opioid analgesics. MOR induces analgesia through the inhibition of second messenger pathways and the modulation of ion channels activity. Nevertheless, cellular excitation has also been demonstrated, and proposed to mediate reduction of therapeutic efficacy and opioid-induced hyperalgesia upon prolonged exposure to opioids. In this mini-perspective, we review the recently identified, functional MOR isoform subclass, which consists of six transmembrane helices (6TM) and may play an important role in MOR signaling. There is evidence that 6TM MOR signals through very different cellular pathways and may mediate excitatory cellular effects rather than the classic inhibitory effects produced by the stimulation of the major (7TM) isoform. Therefore, the development of 6TM and 7TM MOR selective compounds represents a new and exciting opportunity to better understand the mechanisms of action and the pharmacodynamic properties of a new class of opioids. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:61 / 67
页数:7
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