Neural Regeneration Research ›› 2020, Vol. 15 ›› Issue (5): 903-911.doi: 10.4103/1673-5374.268973

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Selective brain hypothermia-induced neuroprotection against focal cerebral ischemia/reperfusion injury is associated with Fis1 inhibition

Ya-Nan Tang1, Gao-Feng Zhang1, Huai-Long Chen1, Xiao-Peng Sun1, Wei-Wei Qin1, Fei Shi1, Li-Xin Sun1, Xiao-Na Xu2, Ming-Shan Wang1   

  1. 1 Department of Anesthesiology, Affiliated Qingdao Municipal Hospital of Qingdao University, Qingdao, Shandong Province, China
    2 Department of Central Laboratory, Affiliated Qingdao Municipal Hospital of Qingdao University, Qingdao, Shandong Province, China
  • Online:2020-05-15 Published:2020-06-01
  • Contact: Ming-Shan Wang, MS,wmsqingdao@163.com.
  • Supported by:
    This study was supported by the Natural Science Foundation of Shandong Province of China, No. ZR2015HM023 (to MSW); the Science and Technology Plan Project of Qingdao City of China, No. 19-6-1-50-nsh (to MSW).

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Abstract: Selective brain hypothermia is considered an effective treatment for neuronal injury after stroke, and avoids the complications of general hypothermia. However, the mechanisms by which selective brain hypothermia affects mitochondrial fission remain unknown. In this study, we investigated the effect of selective brain hypothermia on the expression of fission 1 (Fis1) protein, a key factor in the mitochondrial fission system, during focal cerebral ischemia/reperfusion injury. Sprague-Dawley rats were divided into four groups. In the sham group, the carotid arteries were exposed only. In the other three groups, middle cerebral artery occlusion was performed using the intraluminal filament technique. After 2 hours of occlusion, the filament was slowly removed to allow blood reperfusion in the ischemia/reperfusion group. Saline, at 4°C and 37°C, were perfused through the carotid artery in the hypothermia and normothermia groups, respectively, followed by restoration of blood flow. Neurological function was assessed with the Zea Longa 5-point scoring method. Cerebral infarct volume was assessed by 2,3,5-triphenyltetrazolium chloride staining, and apoptosis was assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling staining. Fis1 and cytosolic cytochrome c levels were assessed by western blot assay. Fis1 mRNA expression was assessed by quantitative reverse transcription-polymerase chain reaction. Mitochondrial ultrastructure was evaluated by transmission electron microscopy. Compared with the sham group, apoptosis, Fis1 protein and mRNA expression and cytosolic cytochrome c levels in the cortical ischemic penumbra and cerebral infarct volume were increased after reperfusion in the other three groups. These changes caused by cerebral ischemia/reperfusion were inhibited in the hypothermia group compared with the normothermia group. These findings show that selective brain hypothermia inhibits Fis1 expression and reduces apoptosis, thereby ameliorating focal cerebral ischemia/reperfusion injury in rats. Experiments were authorized by the Ethics Committee of Qingdao Municipal Hospital of China (approval No. 2019008).

Key words: apoptosis, Fis1, hypothermia, ischemia/reperfusion injury, mitochondria, mitochondrial fission, mitochondrial ultrastructure, neuroprotection, selective brain hypothermia, stroke