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作为疼痛靶点的新型G蛋白偶联受体

Novel G protein-coupled receptors as pain targets.

作者信息

Ahmad Sultan, Dray Andy

机构信息

AstraZeneca Research & Development Montreal, 7171 Frederick Banting St, Montreal H4S 1Z9, Canada.

出版信息

Curr Opin Investig Drugs. 2004 Jan;5(1):67-70.

Abstract

G protein-coupled receptors (GPCRs) and their ligands play a number of important roles in the modulation of acute and chronic pain. Indeed, opioid and cannabinoid ligands are of established therapeutic value for pain management, and further exploitation of the specific GPCR subtypes (delta-opioid, CB1 and CB2) for these ligands may yield more selective, potent analgesics with favorable side effects. More recent identification of a number of other GPCRs involved in pain pathways (eg, sensory neuron specific receptors) and selective ligands that modulate pain transmission, has highlighted further therapeutic opportunities. A further challenge to understanding pain modulation and an additional dimension for targeting analgesia is the discovery of GPCR heteromerization and accessory and regulatory proteins, such as regulator of G protein-signaling proteins, involved in expression and regulation of GPCR.

摘要

G蛋白偶联受体(GPCRs)及其配体在急性和慢性疼痛的调节中发挥着许多重要作用。事实上,阿片类和大麻素类配体在疼痛管理方面具有既定的治疗价值,进一步开发这些配体的特定GPCR亚型(δ-阿片受体、CB1和CB2)可能会产生更具选择性、强效且副作用良好的镇痛药。最近鉴定出了许多参与疼痛通路的其他GPCRs(例如,感觉神经元特异性受体)以及调节疼痛传递的选择性配体,这凸显了更多的治疗机会。理解疼痛调节的另一个挑战以及靶向镇痛的一个新层面是发现GPCR异聚化以及辅助和调节蛋白,如参与GPCR表达和调节的G蛋白信号调节蛋白。

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