受体
类阿片
医学
阿片受体
κ-阿片受体
信号转导
药理学
背景(考古学)
神经科学
δ-阿片受体
细胞生物学
生物
内科学
古生物学
作者
Ream Al‐Hasani,Michael R. Bruchas
出处
期刊:Anesthesiology
[Ovid Technologies (Wolters Kluwer)]
日期:2011-10-21
卷期号:115 (6): 1363-1381
被引量:870
标识
DOI:10.1097/aln.0b013e318238bba6
摘要
Opioid receptors have been targeted for the treatment of pain and related disorders for thousands of years and remain the most widely used analgesics in the clinic. Mu (μ), kappa (κ), and delta (δ) opioid receptors represent the originally classified receptor subtypes, with opioid receptor like-1 (ORL1) being the least characterized. All four receptors are G-protein coupled and activate inhibitory G proteins. These receptors form homo- and heterodimeric complexes and signal to kinase cascades and scaffold a variety of proteins.The authors discuss classic mechanisms and developments in understanding opioid tolerance and opioid receptor signaling and highlight advances in opioid molecular pharmacology, behavioral pharmacology, and human genetics. The authors put into context how opioid receptor signaling leads to the modulation of behavior with the potential for therapeutic intervention. Finally, the authors conclude there is a continued need for more translational work on opioid receptors in vivo.
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