Zhen-Kun Gao, Xin-Ya Shen, Yu Han, Yi-Sha Guo, Kai Li, Xia Bi
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The M1 microglia protein was quantified by western blot and immunofluorescence, and the level of inflammatory factor was measured by enzyme-linked immunosorbent assay. TUNEL staining and western blot were used to measure apoptosis.</p><p><strong>Results: </strong>In the current study, we observed that pre-ischemic exercise effectively decreased infarct volume, neurological deficit score and brain injury in MCAO rats through suppressing the activation of p-JNK and p-ERK1/2. Further investigation revealed that pre-ischemic exercise decreased M1 microglia activation and the serum level of TNF-α and IL-1β. In addition, the increased number of TUNEL-positive cells and Bax/Bcl-2 ratio also were reversed by pre-ischemic exercise.</p><p><strong>Conclusions: </strong>Pre-ischemic exercise can alleviate inflammatory response and apoptosis by inhibiting the MAPK pathway in MCAO rats.</p>","PeriodicalId":23227,"journal":{"name":"Translational Neuroscience","volume":"13 1","pages":"495-505"},"PeriodicalIF":1.8000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803980/pdf/","citationCount":"0","resultStr":"{\"title\":\"Pre-ischemic exercise prevents inflammation and apoptosis by inhibiting MAPK pathway in ischemic stroke.\",\"authors\":\"Zhen-Kun Gao, Xin-Ya Shen, Yu Han, Yi-Sha Guo, Kai Li, Xia Bi\",\"doi\":\"10.1515/tnsci-2022-0268\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Mitogen-activated protein kinase (MAPK) pathway is a major mechanism of acute brain damage in ischemic stroke. 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引用次数: 0
摘要
丝裂原活化蛋白激酶(MAPK)通路是缺血性脑卒中急性脑损伤的一个重要机制。缺血前运动是减轻缺血性损伤的有效方法。然而,在动物模型中,缺血前运动对MAPK通路的调控及其相关机制尚不清楚。材料与方法:本研究将雄性SD大鼠随机分为假手术组、大脑中动脉闭塞(MCAO)组和运动+ MCAO (EX + MCAO)组,观察21 d,然后用MCAO建立。使用Longa评分测量MCAO后0、1、2和3天的神经功能缺损。采用苏木精、伊红染色观察脑损伤。western blot检测MAPK通路的表达。western blot和免疫荧光法测定M1小胶质细胞蛋白,酶联免疫吸附法测定炎症因子水平。TUNEL染色和western blot检测细胞凋亡。结果:在本研究中,我们发现缺血前运动可通过抑制p-JNK和p-ERK1/2的激活,有效降低MCAO大鼠的梗死面积、神经功能缺损评分和脑损伤。进一步研究发现,缺血前运动可降低M1小胶质细胞的活化和血清中TNF-α和IL-1β的水平。此外,缺血前运动也逆转了tunel阳性细胞数量和Bax/Bcl-2比值的增加。结论:缺血前运动可通过抑制MAPK通路减轻MCAO大鼠的炎症反应和细胞凋亡。
Pre-ischemic exercise prevents inflammation and apoptosis by inhibiting MAPK pathway in ischemic stroke.
Introduction: Mitogen-activated protein kinase (MAPK) pathway is a major mechanism of acute brain damage in ischemic stroke. Pre-ischemic exercise is an effective method to reduce ischemic injury. However, the regulation by pre-ischemic exercise of MAPK pathway and associated mechanisms in animal models remains unclear.
Materials and methods: In this study, Male SD rats were randomly divided into sham group, middle cerebral artery occlusion (MCAO) group, and exercise plus MCAO (EX + MCAO) group for 21 days, and then was established by MCAO. Longa score was used to measure neurological deficits at 0, 1, 2, and 3 days after MCAO. Hematoxylin and eosin staining was used to observe the brain injury. The expression of MAPK pathway was quantified by western blot. The M1 microglia protein was quantified by western blot and immunofluorescence, and the level of inflammatory factor was measured by enzyme-linked immunosorbent assay. TUNEL staining and western blot were used to measure apoptosis.
Results: In the current study, we observed that pre-ischemic exercise effectively decreased infarct volume, neurological deficit score and brain injury in MCAO rats through suppressing the activation of p-JNK and p-ERK1/2. Further investigation revealed that pre-ischemic exercise decreased M1 microglia activation and the serum level of TNF-α and IL-1β. In addition, the increased number of TUNEL-positive cells and Bax/Bcl-2 ratio also were reversed by pre-ischemic exercise.
Conclusions: Pre-ischemic exercise can alleviate inflammatory response and apoptosis by inhibiting the MAPK pathway in MCAO rats.
期刊介绍:
Translational Neuroscience provides a closer interaction between basic and clinical neuroscientists to expand understanding of brain structure, function and disease, and translate this knowledge into clinical applications and novel therapies of nervous system disorders.