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小续命汤减轻脑缺血再灌注损伤中的线粒体自噬激活并改善线粒体功能

Xiao-Xu-Ming Decoction Reduced Mitophagy Activation and Improved Mitochondrial Function in Cerebral Ischemia and Reperfusion Injury.

作者信息

Lan Rui, Zhang Yong, Wu Tao, Ma Yun-Zhi, Wang Bao-Qi, Zheng Hai-Zhong, Li Ya-Na, Wang Yan, Gu Chun-Qing, Wu Ji-Tao

机构信息

Encephalopathy Hospital, The First Affiliated Hospital of Henan University of Chinese Medicine, Henan 450000, China.

Cerebral Palsy Rehabilitation Department, The Third Affiliated Hospital of Zhengzhou University, Henan 450000, China.

出版信息

Behav Neurol. 2018 Jun 19;2018:4147502. doi: 10.1155/2018/4147502. eCollection 2018.

Abstract

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.

摘要

我们研究了小续命汤是否能减轻脑缺血再灌注损伤中的线粒体自噬激活并维持线粒体功能。将大鼠随机分为5组:假手术组、缺血再灌注(IR)组、IR加小续命汤(60 g/kg/天)(XXMD60)组、IR加环孢素A(10 mg/kg/天)(CsA)组和IR加溶媒(溶媒)组。采用大脑中动脉闭塞(MCAO)法诱导局灶性脑缺血再灌注模型。通过氯化三苯基四氮唑染色测量脑梗死面积。通过苏木精-伊红染色(HE)和尼氏染色评估脑缺血损伤。通过透射电子显微镜观察缺血皮层半暗带中线粒体和线粒体自噬的超微结构特征。通过用LC3B和VDAC1进行免疫荧光标记检测线粒体自噬。通过用LC3B和Lamp1进行免疫荧光标记观察自噬溶酶体形成。通过蛋白质免疫印迹法分析LC3B、Beclin1和Lamp1的表达。接受MCAO的大鼠神经功能评分恶化且细胞缺血损伤加重。这些均被小续命汤或CsA显著逆转。此外,小续命汤/CsA显著下调线粒体自噬,并减少脑缺血再灌注诱导的LC3、Beclin1和Lamp1表达增加。研究结果表明,小续命汤通过下调LC3、Beclin1、Lamp1和线粒体p62表达水平发挥神经保护作用,从而抑制线粒体自噬。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ecc/6029470/e7de85b662f0/BN2018-4147502.001.jpg

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