Challenges for opioid receptor nomenclature: IUPHAR Review 9

被引:99
作者
Cox, Brian M. [1 ]
Christie, Macdonald J. [2 ]
Devi, Lakshmi [3 ]
Toll, Lawrence [4 ]
Traynor, John R. [5 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Pharmacol, Bethesda, MD 20814 USA
[2] Univ Sydney, Sydney Med Sch, Discipline Pharmacol, Sydney, NSW 2006, Australia
[3] Icahn Sch Med Mt Sinai, Dept Pharmacol & Syst Therapeut, New York, NY 10029 USA
[4] Torrey Pines Inst Mol Studies, Port St Lucie, FL USA
[5] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
关键词
TERMINAL SPLICE VARIANTS; NALORPHINE-LIKE DRUGS; CHRONIC SPINAL DOG; G-PROTEIN; KNOCKOUT MICE; MORPHINE-LIKE; RAT-BRAIN; MU; DELTA; PHARMACOLOGY;
D O I
10.1111/bph.12612
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent developments in the study of the structure and function of opioid receptors raise significant challenges for the definition of individual receptor types and the development of a nomenclature that precisely describes isoforms that may subserve different functions in vivo. Presentations at the 2013 meeting of the International Narcotics Research Conference in Cairns, Australia, considered some of the new discoveries that are now unravelling the complexities of opioid receptor signalling. Variable processing of opioid receptor messenger RNAs may lead to the presence of several isoforms of the receptor. Each opioid receptor type can function either as a monomer or as part of a homo- or heterodimer or higher multimer. Additionally, recent evidence points to the existence of agonist bias in the signal transduction pathways activated through receptors, and to the presence of regulatory allosteric sites on the receptors. This brief review summarizes the recent discoveries that raise challenges for receptor definition and the characterization of signal transduction pathways activated by specific receptor forms. Linked ArticlesThis article is part of a themed section on Opioids: New Pathways to Functional Selectivity. To view the other articles in this section visit
引用
收藏
页码:317 / 323
页数:7
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