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GPR55激活可改善小鼠甲基苯丙胺戒断期间的焦虑样和抑郁样行为。

GPR55 activation improves anxiety- and depression-like behaviors of mice during methamphetamine withdrawal.

作者信息

Zhang Jinlong, Yan Jie, Li Shuyue, Chen Qianqian, Lin Jiang, Peng Yilin, Liu Yuhang, Wang Binbin, Wei Xinrong, Sun Chen, Niu Shuliang

机构信息

Department of Forensic Science, School of Basic Medical Science, Xinjiang Medical University, Urumqi, 830011, China.

Department of Forensic Science, School of Basic Medical Science, Central South University, Changsha, 410000, China.

出版信息

Heliyon. 2024 Apr 27;10(9):e30462. doi: 10.1016/j.heliyon.2024.e30462. eCollection 2024 May 15.

Abstract

Methamphetamine is a potent and highly addictive neurotoxic psychostimulant that triggers a spectrum of adverse emotional responses during withdrawal. G-protein coupled receptor 55 (GPR55), a novel endocannabinoid receptor, is closely associated with mood regulation. Herein, we developed a murine model of methamphetamine-induced anxiety- and depressive-like behavior during abstinence which showed a decreased GPR55 expression in the hippocampus. Activation of GPR55 mitigated these behavioral symptoms, concomitantly ameliorating impairments in hippocampal neurogenesis and reducing neuroinflammation. These findings underscore the pivotal role of GPR55 in mediating the neuropsychological consequences of methamphetamine withdrawal, potentially via mechanisms involving the modulation of hippocampal neurogenesis and inflammation.

摘要

甲基苯丙胺是一种强效且极易成瘾的神经毒性精神兴奋剂,在戒断期间会引发一系列不良情绪反应。G蛋白偶联受体55(GPR55)是一种新型内源性大麻素受体,与情绪调节密切相关。在此,我们建立了一个甲基苯丙胺诱导的禁欲期间焦虑和抑郁样行为的小鼠模型,该模型显示海马体中GPR55表达降低。激活GPR55可减轻这些行为症状,同时改善海马体神经发生的损伤并减少神经炎症。这些发现强调了GPR55在介导甲基苯丙胺戒断的神经心理后果中的关键作用,可能是通过涉及调节海马体神经发生和炎症的机制来实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1f/11077030/86dccf86bac6/gr1.jpg

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