首页> 外文期刊>International journal of molecular medicine >Treadmill exercise promotes neurogenesis and myelin repair via upregulating Wnt/beta-catenin signaling pathways in the juvenile brain following focal cerebral ischemia/reperfusion
【24h】

Treadmill exercise promotes neurogenesis and myelin repair via upregulating Wnt/beta-catenin signaling pathways in the juvenile brain following focal cerebral ischemia/reperfusion

机译:跑步机促进神经发生和髓鞘修复通过在局灶性脑缺血/再灌注之后的少年脑中的WNT /β-连环蛋白信号传导途径促进神经发生和髓鞘修复

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Physical exercise has a neuroprotective effect and is an important treatment after ischemic stroke. Promoting neurogenesis and myelin repair in the penumbra is an important method for the treatment of ischemic stroke. However, the role and potential mechanism of exercise in neurogenesis and myelin repair still needs to be clarified. The goal of the present study was to ascertain the possible effect of treadmill training on the neuroprotective signaling pathway in juvenile rats after ischemic stroke. The model of middle cerebral artery occlusion (MCAO) in juvenile rats was established and then the rats were randomly divided into 9 groups. XAV939 (an inhibitor of the Wnt/beta -catenin pathway) was used to confirm the effects of the Wnt/beta -catenin signaling pathway on exercise-mediated neurogenesis and myelin repair. Neurological deficits were detected by modified neurological severity score, the injury of brain tissue and the morphology of neurons was detected by hematoxylin-eosin staining and Nissl staining, and the infarct volume was detected by 2,3,5-triphenyl tetrazolium chloride staining. The changes in myelin were observed by Luxol fast blue staining. The neuron ultrastructure was observed by transmission electron microscopy. Immunofluorescence and western blots analyzed the molecular mechanisms. The results showed that treadmill exercise improved neurogenesis, enhanced myelin repair, promoted neurological function recovery and reduced infarct volume. These were the results of the upregulation of Wnt3a and nucleus beta -catenin, brain-derived neurotrophic factor (BDNF) and myelin basic protein (MBP). In addition, XAV939 inhibited treadmill exercise-induced neurogenesis and myelin repair, which was consistent with the downregulation of Wnt3a, nucleus beta -catenin, BDNF and MBP expression, and the deterioration of neurological function. In summary, treadmill exercise promotes neurogenesis and myelin repair by upregulating the Wnt/beta -catenin signaling pathway, to improve the neurological deficit caused by focal cerebral ischemia/reperfusion.
机译:体育锻炼具有神经保护作用,并且在缺血性中风后是一个重要的治疗方法。促进神经发生和髓鞘修复在Penumbra中是治疗缺血性卒中的重要方法。但是,需要澄清神经发生和髓鞘修复中运动的作用和潜在机制。本研究的目标是确定跑步机训练在缺血性卒中后少年大鼠神经保护信号通路的可能影响。建立了少年大鼠中脑动脉闭塞(MCAO)的模型,然后将大鼠随机分为9组。 XAV939(WNT /β-Catenin途径的抑制剂)用于确认WNT /β-Catenin信号传导途径对运动介导的神经发生和髓鞘修复的影响。通过修饰的神经严重程度评分检测神经系统缺陷,通过苏木精 - 曙红染色和NISL染色检测脑组织的损伤和神经元的形态,并通过2,3,5-三苯基四唑氯化物染色检测梗塞体积。 Luxol Fast Blue染色观察了髓鞘的变化。通过透射电子显微镜观察神经元超微结构。免疫荧光和Western印迹分析了分子机制。结果表明,跑步机锻炼改善神经发生,增强髓鞘修复,促进神经功能恢复和减少梗塞体积。这些是Wnt3a和核β-catenin,脑衍生的神经营养因子(bdnf)和髓鞘碱性蛋白(Mbp)的上调的结果。此外,XAV939抑制跑步机诱导的神经发生和髓鞘修复,这与WNT3A,核β-肽,BDNF和MBP表达的下调以及神经功能的恶化一致。总之,跑步机练习通过上调WNT /β-Catenin信号通路来促进神经发生和髓鞘修复,以改善局灶性脑缺血/再灌注引起的神经缺陷。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号