Exercise preconditioning mitigates brain injury after cerebral ischemia-reperfusion injury in rats by restraining TIMP1

被引:0
|
作者
Meng, Xiangbo [1 ]
Yang, Hui [2 ]
Chen, Feifeng [3 ]
Li, Baohua [2 ]
Wu, Yan [3 ]
Wang, Rong [4 ]
机构
[1] Hangzhou Normal Univ, Affiliated Hosp, Dept Rehabil Med, Hangzhou 310000, Zhejiang, Peoples R China
[2] Hangzhou First Peoples Hosp, Dept Neurol, Hangzhou 310006, Zhejiang, Peoples R China
[3] Hangzhou First Peoples Hosp, Dept Rehabil Med, Hangzhou 310006, Zhejiang, Peoples R China
[4] Hangzhou First Peoples Hosp, Dept Radiol, 261 Huansha Rd, Hangzhou 310006, Zhejiang, Peoples R China
关键词
brain injury; cerebral ischemia-reperfusion injury; exercise preconditioning; TIMP1; SIGNALING PATHWAY; REGENERATION; APOPTOSIS; MIRNA-210; STROKE; CELLS;
D O I
10.1002/iid3.70008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundCerebral ischemic disease is a common cerebrovascular disease, especially ischemic stroke. Exercise has protective functions on brain tissues following cerebral ischemia-reperfusion injury (CIRI), but its preventive effects and mechanisms in CIRI remain unclear. We aimed to investigate the effects and mechanisms of exercise preconditioning on CIRI.MethodsThe middle cerebral artery occlusion (MCAO) operation was prepared to establish CIRI rats. All rats were randomized into the MCAO, exercise (exercise preconditioning plus MCAO operation), vector (exercise preconditioning, MCAO operation plus intraventricular injection of empty vector), and tissue inhibitor of metalloprotease 1 overexpression (OE-TIMP1, exercise preconditioning, MCAO operation plus intraventricular injection of OE-TIMP1) groups.ResultsThe results indicated that exercise preconditioning suppressed approximately 66.67% of neurological deficit scores and 73.79% of TIMP1 mRNA expression in MCAO rats, which were partially offset by OE-TIMP1. The protective effects of exercise against neuron death status and cerebral infarction size in MCAO rats were reversed by OE-TIMP1. It also confirmed that exercise weakened apoptosis and oxidative stress damage, with notable increases of B-cell lymphoma-2, superoxide dismutase, and glutathione peroxidase production, and evident decreases of BCL2-associated X, caspase 3, and malondialdehyde in MCAO rats, while these effects were partially reversed by OE-TIMP1. Additionally, the inhibitory effects of exercise on the protein levels of TIMP1, hypoxia-inducible factor-alpha, vascular endothelial growth factor receptor 2, vascular endothelial growth factor, and neurogenic locus notch homolog protein 1 in MCAO rats were partially reversed by OE-TIMP1.ConclusionAltogether, exercise preconditioning had protective effects on CIRI by restraining TIMP1, which provided new therapeutic strategies for preventing CIRI. We found that exercise preconditioning had protective effects on CIRI by restraining TIMP1, which provides new targets and therapeutic strategies for the prevention of CIRI. image
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页数:13
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