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电针改善阿尔茨海默病海马区M2小胶质细胞极化及胶质细胞抗炎作用。

Electroacupuncture Improves M2 Microglia Polarization and Glia Anti-inflammation of Hippocampus in Alzheimer's Disease.

作者信息

Xie Lushuang, Liu Yi, Zhang Ning, Li Chenyu, Sandhu Aaron F, Williams George, Shen Yan, Li Hongying, Wu Qiaofeng, Yu Shuguang

机构信息

College of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Institute of Electroacupuncture and Homeostasis Regulation, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Neurosci. 2021 Sep 27;15:689629. doi: 10.3389/fnins.2021.689629. eCollection 2021.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disease characterized by loss of recognition and memory. Neuroinflammation plays pivotal roles in the pathology of AD and affects the progression of the disease. Astrocyte and microglia, as main immune executors in the central nervous system (CNS), participate into the inflammatory response in AD. Glia polarize into different phenotypes during neurodegeneration. Pro-inflammatory glia produce cytokines (IL-1β, TNF-α, and IL-6) resulting into debris aggregates and neurotoxicity. Anti-inflammatory phenotypes produce cytokines (IL-4 and IL-10) to release the inflammation. Electroacupuncture is a useful treatment that has been found to slow the neurodegeneration in animals through experimentation and in humans through clinical trials. The aim of this study was to uncover the mechanisms of glia activation, microglia polarization, and cytokine secretion regulated by electroacupuncture as a treatment for AD. Twenty male Sprague-Dawley (SD) rats were randomly divided into four groups: Control group (Control), Normal saline group (NS), AD group (AD), and Electroacupuncture group (Acupuncture). The AD and Acupuncture groups were bilaterally injected with Aβ into the CA1 field of the hippocampus. The Acupuncture group received electroacupuncture stimulation on the acupoint "Baihui" (GV20) for 6 days per week for a total of 3 weeks. The Morris Water Maze (MWM) was used to evaluate learning and memory capacity. Immunofluorescence was used to stain GFAP and Iba1 of the DG and CA1 in the hippocampus, which, respectively, expressed the activation of astrocyte and microglia. The M1 microglia marker, inducible nitric oxide synthase (iNOS), and M2 marker Arginase 1 (Arg1) were used to analyze the polarization of microglia. The pro-inflammatory cytokines (IL-1β, TNF-α, and IL-6), anti-inflammatory cytokines (IL-4 and IL-10), and pathway-molecules (p65 and Stat6) were tested to analyze the glia inflammatory response by immunofluorescence and polymerase chain reaction (PCR). The MWM results showed that electroacupuncture improves the escape latency time and the swimming distance of AD rats. The number of GFAP and Iba1 cells significantly increased in AD rats, but electroacupuncture decreased the cells. The iNOS-positive cells were significantly increased in AD, and electroacupuncture decreased the positive cells. Electroacupuncture elevated Arg1-positive cells in AD rats. Electroacupuncture decreased the glia pro-inflammatory cytokine expression and increased the anti-inflammatory cytokine expression in AD rats. Furthermore, electroacupuncture inhibited the NF-κB pathway molecule (p65) while raising the Stat6 pathway molecule (Stat6). These results provide evidence that electroacupuncture improves the recognition abilities and memory of AD rats. Electroacupuncture inhibits the activation of glia and polarizes microglia toward the M2 phenotype. Electroacupuncture decreased the pro-inflammatory cytokines (IL-1β, TNF-α, and IL-6) and increased the anti-inflammatory cytokines (IL-4 and IL-10). Furthermore, electroacupuncture affects the immune responses through inhibition of NF-κB pathway but activation of Stat6 pathway.

摘要

阿尔茨海默病(AD)是一种以认知和记忆丧失为特征的神经退行性疾病。神经炎症在AD的病理过程中起关键作用,并影响疾病的进展。星形胶质细胞和小胶质细胞作为中枢神经系统(CNS)中的主要免疫执行者,参与AD中的炎症反应。在神经退行性变过程中,胶质细胞会极化为不同的表型。促炎性胶质细胞产生细胞因子(IL-1β、TNF-α和IL-6),导致碎片聚集和神经毒性。抗炎表型产生细胞因子(IL-4和IL-10)以减轻炎症。电针是一种有效的治疗方法,通过实验已发现其可减缓动物的神经退行性变,通过临床试验也证实其对人类有效。本研究的目的是揭示电针治疗AD时调节胶质细胞激活、小胶质细胞极化和细胞因子分泌的机制。将20只雄性Sprague-Dawley(SD)大鼠随机分为四组:对照组(Control)、生理盐水组(NS)、AD组(AD)和电针组(Acupuncture)。AD组和电针组双侧海马CA1区注射Aβ。电针组每周6天在穴位“百会”(GV20)接受电针刺激,共3周。采用Morris水迷宫(MWM)评估学习和记忆能力。免疫荧光法对海马齿状回(DG)和CA1区的GFAP和Iba1进行染色,分别表示星形胶质细胞和小胶质细胞的激活情况。使用M1小胶质细胞标志物诱导型一氧化氮合酶(iNOS)和M2标志物精氨酸酶1(Arg1)分析小胶质细胞的极化情况。通过免疫荧光和聚合酶链反应(PCR)检测促炎细胞因子(IL-1β、TNF-α和IL-6)、抗炎细胞因子(IL-4和IL-10)以及信号通路分子(p65和Stat6),以分析胶质细胞炎症反应。MWM结果显示,电针可改善AD大鼠的逃避潜伏期和游泳距离。AD大鼠中GFAP和Iba1细胞数量显著增加,但电针减少了这些细胞数量。AD大鼠中iNOS阳性细胞显著增加,电针减少了阳性细胞数量。电针增加了AD大鼠中Arg1阳性细胞数量。电针降低了AD大鼠中胶质细胞促炎细胞因子的表达,增加了抗炎细胞因子的表达。此外,电针抑制了NF-κB信号通路分子(p65),同时上调了Stat6信号通路分子(Stat6)。这些结果表明,电针可改善AD大鼠的认知能力和记忆力。电针抑制胶质细胞的激活,并使小胶质细胞向M2表型极化。电针降低了促炎细胞因子(IL-1β、TNF-α和IL-6)的水平,增加了抗炎细胞因子(IL-4和IL-10)的水平。此外,电针通过抑制NF-κB信号通路但激活Stat6信号通路来影响免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2633/8502881/5d82c2b19899/fnins-15-689629-g001.jpg

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