首页> 美国卫生研究院文献>Behavioural Neurology >Xiao-Xu-Ming Decoction Reduced Mitophagy Activation and Improved Mitochondrial Function in Cerebral Ischemia and Reperfusion Injury
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Xiao-Xu-Ming Decoction Reduced Mitophagy Activation and Improved Mitochondrial Function in Cerebral Ischemia and Reperfusion Injury

机译:消虚明汤在脑缺血再灌注损伤中减少线粒体激活并改善线粒体功能

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摘要

We investigated whether Xiao-Xu-Ming decoction reduced mitophagy activation and kept mitochondrial function in cerebral ischemia-reperfusion injury. Rats were randomly divided into 5 groups: sham, ischemia and reperfusion (IR), IR plus XXMD (60 g/kg/day) (XXMD60), IR plus cyclosporin A (10 mg/kg/day) (CsA), and IR plus vehicle (Vehicle). Focal cerebral ischemia and reperfusion models were induced by middle cerebral artery occlusion (MCAO). Cerebral infarct areas were measured by triphenyl tetrazolium chloride staining. Cerebral ischemic injury was evaluated by hematoxylin and eosin staining (HE) and Nissl staining. Ultrastructural features of mitochondria and mitophagy in the penumbra of the ischemic cortex were observed by transmission electron microscopy. Mitophagy was detected by immunofluorescence labeled with LC3B and VDAC1. Autophagy lysosome formation was observed by immunofluorescence labeled with LC3B and Lamp1. The expression of LC3B, Beclin1, and Lamp1 was analyzed by Western blot. The rats subjected to MCAO showed worsened neurological score and cell ischemic damage. These were all significantly reversed by XXMD or CsA. Moreover, XXMD/CsA notably downregulated mitophagy and reduced the increase in LC3, Beclin1, and Lamp1 expression induced by cerebral ischemia and reperfusion. The findings demonstrated that XXMD exerted neuroprotective effect via downregulating LC3, Beclin1, Lamp1, and mitochondrial p62 expression level, thus leading to the inhibition of mitophagy.
机译:我们研究了小徐明汤在脑缺血-再灌注损伤中是否降低了线粒体的激活并保持了线粒体功能。大鼠随机分为5组:假手术,缺血和再灌注(IR),IR加XXMD(60μg/ kg /天)(XXMD60),IR加环孢菌素A(10μmg/ kg /天)(CsA)和IR加上车辆(车辆)。大脑中动脉闭塞(MCAO)诱发局灶性脑缺血和再灌注模型。通过三苯基氯化四氮唑染色测量脑梗塞区域。用苏木精和曙红染色(HE)和尼氏染色评估脑缺血损伤。通过透射电镜观察了缺血皮层半影线粒体的超微结构特征和线粒体。通过LC3B和VDAC1标记的免疫荧光检测线粒体。通过用LC3B和Lamp1标记的免疫荧光观察到自噬溶酶体的形成。通过蛋白质印迹分析LC3B,Beclin1和Lamp1的表达。接受MCAO的大鼠表现出神经学评分恶化和细胞缺血损伤。这些都被XXMD或CsA显着逆转。此外,XXMD / CsA显着下调了线粒体吞噬并减少了脑缺血和再灌注诱导的LC3,Beclin1和Lamp1表达的增加。这些发现表明,XXMD通过下调LC3,Beclin1,Lamp1和线粒体p62的表达水平发挥神经保护作用,从而导致线粒体的抑制。

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