甲基苯丙胺
细胞凋亡
小胶质细胞
细胞生物学
程序性细胞死亡
蛋白激酶B
激酶
受体
化学
信号转导
生物
药理学
免疫学
生物化学
炎症
作者
Kai Shen,Yuan Zhang,Xuan Lv,Xufeng Chen,Rongbin Zhou,Lan K. Nguyen,Xiaodong Wu,Honghong Yao
出处
期刊:Cns & Neurological Disorders-drug Targets
[Bentham Science]
日期:2016-05-19
卷期号:15 (7): 857-865
被引量:17
标识
DOI:10.2174/1871527315666160518122816
摘要
It has been well documented that methamphetamine induces microglial activation and death, however, the molecular mechanisms underlying this process remain poorly understood. In the present study, we demonstrated the involvement of sigma-1 receptor (σ-1R) in methamphetamine-mediated microglial apoptosis. Exposure of BV-2 cells to methamphetamine induces cell apoptosis through its cognate receptor σ-1R, followed by activation of the mitogen-activated protein kinases, phosphatidylinositol-3' kinase/Akt as well as the downstream transcription factor p53 pathways. Blockage of σ -1R significantly inhibited the increased pro-apoptotic proteins such as Bax, Caspase-3 and Caspase-9 induced by methamphetamine. In conclusion, these findings underscore the critical role of σ-1R in microglial apoptosis induced by methamphetamine. Understanding the link between σ -1R and apoptosis will lead to development of therapeutic strategies targeting methamphetamine-mediated microglial death/dysfunction. Keywords: Apoptosis, σ-1R, methamphetamine, microglia.
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