首页> 美国卫生研究院文献>International Journal of Molecular Medicine >Treadmill exercise promotes neurogenesis and myelin repair via upregulating Wnt/β-catenin signaling pathways in the juvenile brain following focal cerebral ischemia/reperfusion
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Treadmill exercise promotes neurogenesis and myelin repair via upregulating Wnt/β-catenin signaling pathways in the juvenile brain following focal cerebral ischemia/reperfusion

机译:跑步机运动可通过上调局灶性脑缺血/再灌注后少年大脑中的Wnt /β-catenin信号通路来促进神经发生和髓鞘修复

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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/β-catenin pathway) was used to confirm the effects of the Wnt/β-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 β-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 β-catenin, BDNF and MBP expression, and the deterioration of neurological function. In summary, treadmill exercise promotes neurogenesis and myelin repair by upregulating the Wnt/β-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,是缺血性中风后的重要治疗方法。促进半影的神经发生和髓鞘修复是治疗缺血性中风的重要方法。但是,运动在神经发生和髓鞘修复中的作用和潜在机制仍有待阐明。本研究的目的是确定跑步机训练对缺血性中风后幼年大鼠神经保护信号通路的可能作用。建立幼年大鼠大脑中动脉闭塞模型(MCAO),然后将大鼠随机分为9组。 XAV939(Wnt /β-catenin途径的抑制剂)被用于证实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。用改良的神经系统严重程度评分法检测神经功能缺损,用苏木精-伊红染色和尼氏染色法检测脑组织损伤和神经元形态,用2,3,5-三苯基氯化四氮唑蓝染色法测定梗死面积。通过Luxol坚牢蓝染色观察到髓磷脂的变化。通过透射电子显微镜观察神经元超微结构。免疫荧光和蛋白质印迹分析了分子机制。结果表明,跑步机锻炼可改善神经发生,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β-catenin核,脑源性神经营养因子(BDNF)和髓鞘碱性蛋白(MBP)上调的结果。此外,XAV939抑制了跑步机运动引起的神经发生和髓鞘修复,这与Wnt3a,β-catenin核,BDNF和MBP表达下调以及神经功能恶化有关。总之,跑步机运动通过上调Wnt /β-catenin信号通路来促进神经发生和髓鞘修复,从而改善由局灶性脑缺血/再灌注引起的神经功能缺损。

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