星形胶质细胞CB1R的激活介导电针诱导的脑缺血耐受。

Cen Yang, Jingjing Liu, Jingyi Wang, Anqi Yin, Zhenhua Jiang, Shuwei Ye, Xue Liu, Xia Zhang, Feng Wang, Lize Xiong
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引用次数: 14

摘要

中风没有有效的治疗方法。激活内源性保护机制是一种很有前途的治疗方法,它唤起了大脑保护自身的内在能力。越来越多的证据表明,电针(EA)预处理可诱导脑缺血快速耐受。EA诱导缺血耐受的机制涉及许多分子和信号通路,如内源性大麻素系统,但其确切机制尚未完全阐明。在当前的研究中,我们采用突变小鼠、神经药理学、微透析和病毒转染技术在大脑中动脉闭塞(MCAO)模型中探索ea诱导的神经保护的细胞特异性和脑区域特异性机制。EA预处理导致环境内源性大麻素(eCB)水平升高,随后缺血半暗区星形胶质大麻素1型受体(CB1R)激活,导致细胞外谷氨酸适度上调,保护神经元免受缺血性脑损伤。这些发现提供了一种新的EA细胞机制和缺血性脑卒中的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Activation of astroglial CB1R mediates cerebral ischemic tolerance induced by electroacupuncture.

Activation of astroglial CB1R mediates cerebral ischemic tolerance induced by electroacupuncture.

Activation of astroglial CB1R mediates cerebral ischemic tolerance induced by electroacupuncture.

There are no effective treatments for stroke. The activation of endogenous protective mechanisms is a promising therapeutic approach, which evokes the intrinsic ability of the brain to protect itself. Accumulated evidence strongly suggests that electroacupuncture (EA) pretreatment induces rapid tolerance to cerebral ischemia. With regard to mechanisms underlying ischemic tolerance induced by EA, many molecules and signaling pathways are involved, such as the endocannabinoid system, although the exact mechanisms have not been fully elucidated. In the current study, we employed mutant mice, neuropharmacology, microdialysis, and virus transfection techniques in a middle cerebral artery occlusion (MCAO) model to explore the cell-specific and brain region-specific mechanisms of EA-induced neuroprotection. EA pretreatment resulted in increased ambient endocannabinoid (eCB) levels and subsequent activation of ischemic penumbral astroglial cannabinoid type 1 receptors (CB1R) which led to moderate upregulation of extracellular glutamate that protected neurons from cerebral ischemic injury. These findings provide a novel cellular mechanism of EA and a potential therapeutic target for ischemic stroke.

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