电针通过调节小胶质细胞的激活和极化,促进脑缺血大鼠胼胝体区域髓磷脂的修复。

IF 1.5 4区 医学 Q3 CLINICAL NEUROLOGY
Wei Wang, Cuicui Chan, Xiuxiu Wang, Feng Wu
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引用次数: 0

摘要

背景:缺血性中风可损伤脑白质,导致髓磷脂丢失和神经功能缺损。此外,小胶质细胞激活在缺血性卒中中起重要作用;因此,抑制小胶质细胞活化已成为缺血性脑卒中的有效治疗靶点。目的:探讨电针(EA)对缺血性脑卒中后小胶质细胞激活和极化的影响,以及少突胶质细胞发生在髓鞘重组中的作用。方法:建立永久性大脑中动脉闭塞(p-MCAO)大鼠模型,采用筑巢法、Luxol快速蓝染色、免疫荧光染色和Western blot观察EA对p-MCAO大鼠胼胝体(CC)损伤的修复作用。采用实时定量聚合酶链反应检测炎症因子IL-1β和IL-10的表达水平。结果:p-MCAO大鼠筑巢能力明显受损,CC区髓磷脂严重丢失,Olig2蛋白表达减少,小胶质细胞活化,以m1型小胶质细胞极化为主。EA治疗改善了筑巢行为,减轻了髓磷脂损失,增强了Olig2表达,抑制了过度的小胶质细胞激活,下调了IL-1β,上调了IL-10表达水平。结论:这些发现表明,EA通过抑制M1小胶质细胞极化、诱导M2表型转移、调节炎症反应和促进少突胶质细胞再生,促进缺血脑白质髓磷脂修复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electroacupuncture promotes myelin repair in the corpus callosum region of cerebral ischemic rats by modulating microglia activation and polarization.

Background: Ischemic stroke can damage the cerebral white matter, resulting in myelin loss and neurological deficits. Moreover, microglial activation plays an important role in ischemic stroke; therefore, inhibiting microglial activation has become an effective therapeutic target for ischemic stroke.

Objective: This study aimed to investigate the effects of electroacupuncture (EA) on microglial activation and polarization, and the role of oligodendrocyte genesis in myelin reformation after ischemic stroke.

Methods: A rat model of permanent middle cerebral artery occlusion (p-MCAO) was established and treated with EA. The reparative effect of EA on corpus callosum (CC) injury in p-MCAO rats was evaluated using a nesting assay, Luxol fast blue staining, immunofluorescence staining, and Western blot. Additionally, quantitative real-time polymerase chain reaction was employed to measure inflammatory factors IL-1β and IL-10 expression levels.

Results: The results showed that p-MCAO rats exhibited significantly impaired nesting ability, severe myelin loss in the CC region, reduced Olig2 protein expression, activated microglia, and predominately M1-type microglial polarization. EA treatment improved nesting behavior, mitigated myelin loss, enhanced Olig2 expression, suppressed excessive microglial activation, downregulated IL-1β, and upregulated IL-10 expression levels.

Conclusions: These findings indicate that EA facilitates myelin repair in ischemic cerebral white matter by suppressing M1 microglial polarization, inducing an M2 phenotypic shift, modulating inflammatory responses, and enhancing oligodendrocyte regeneration.

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来源期刊
Neurological Research
Neurological Research 医学-临床神经学
CiteScore
3.60
自引率
0.00%
发文量
116
审稿时长
5.3 months
期刊介绍: Neurological Research is an international, peer-reviewed journal for reporting both basic and clinical research in the fields of neurosurgery, neurology, neuroengineering and neurosciences. It provides a medium for those who recognize the wider implications of their work and who wish to be informed of the relevant experience of others in related and more distant fields. The scope of the journal includes: •Stem cell applications •Molecular neuroscience •Neuropharmacology •Neuroradiology •Neurochemistry •Biomathematical models •Endovascular neurosurgery •Innovation in neurosurgery.
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