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大脑中的 GPR55 与慢性神经性疼痛。

GPR55 in the brain and chronic neuropathic pain.

机构信息

Department of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, School of Medicine Lubbock, TX, 79430, United States.

Center for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, 19140, United States.

出版信息

Behav Brain Res. 2021 May 21;406:113248. doi: 10.1016/j.bbr.2021.113248. Epub 2021 Mar 18.

Abstract

There is a clear need for novel and improved therapeutic strategies for alleviating chronic neuropathic pain, as well as a need for better understanding of brain mechanisms of neuropathic pain, which are less understood than spinal and peripheral mechanisms. The G protein-coupled receptor 55 (GPR55), is a lysophosphatidylinositol (LPI)-sensitive receptor that has also been involved in cannabinoid signaling. It is expressed throughout the central nervous system, including the periaqueductal gray (PAG), a brainstem area and key element of the descending pain control system. Behaviors, pharmacology, biochemistry tools, and stereotaxic microinjections were used to determine if GPR55 plays a role in pain control in a chronic constriction injury (CCI) neuropathic pain model in rats. It was found that the blockade of GPR55 action in the PAG can restore and drive a descending control system to mitigate neuropathic pain. Our data demonstrate that GPR55 play a role in the descending pain control system, and identify GPR55 at supraspinal level as a neuropathic pain brain mechanism.

摘要

目前,人们急需新型、改良的治疗策略来缓解慢性神经性疼痛,同时也需要更好地理解神经性疼痛的大脑机制,这些机制比脊髓和外周机制的理解程度要低。G 蛋白偶联受体 55(GPR55)是一种溶血磷脂酰肌醇(LPI)敏感受体,也参与了大麻素信号转导。它在中枢神经系统中广泛表达,包括中脑导水管周围灰质(PAG),这是一个脑干区域,也是下行疼痛控制系统的关键组成部分。研究人员使用行为学、药理学、生物化学工具和立体定向微注射来确定 GPR55 是否在慢性缩窄性损伤(CCI)神经性疼痛模型大鼠的疼痛控制中发挥作用。结果发现,PAG 中 GPR55 作用的阻断可以恢复并驱动下行控制系统来减轻神经性疼痛。我们的数据表明,GPR55 在下行疼痛控制系统中发挥作用,并确定了位于脊髓以上水平的 GPR55 作为神经性疼痛的大脑机制。

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