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Functional role of HIF-1α in hypoxic preconditioning-induced neuroprotection against focal cerebral ischemia

机译:HIF-1α在缺氧预处理诱导的神经保护作用对局灶性脑缺血的功能作用

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Objective To investigate the expression of HIF-1α after permcnent focal cerebral ischemia and to explore the role of HIF-la in hypoxic preconditioning-induced neuroprotection. Methods Rat focal cerebral ischemia model and hypoxic preconditioning models were established. Animals were randomly divided into four groups: healthy control, hypoxic preconditioning (3 h of 8% O_2/92% N_2 treatment), focal cerebral ischemia (6 h, 1 d, 3 d or 7 d) and hypoxic preconditioning + focal cerebral ischemia (6 h, 1 d, 3 d or 7 d). The expression of HIF-1α after different treatments was determined by histological examination, immunohistochemistry and in situ hybridization. Results The mRNA and protein expressions of HIF-1α could be detected in survival and necrotic neurons, glia as well as vascular endothelial cells. Hypoxic preconditioning significantly promoted the expression of HIF-1α after focal cerebral ischemia, especially in ischemic peripheral zone (P < 0.05).
机译:目的探讨HIF-1α在渗透局灶性脑缺血后的表达,探讨HIF-LA在缺氧预处理诱导的神经保护中的作用。方法建立了大鼠局灶性脑缺血模型和缺氧预处理模型。将动物随机分为四组:健康对照,缺氧预处理(3小时,8%O_2 / 92%N_2处理),局灶性脑缺血(6小时,1d,3d或7d)和缺氧预处理+局灶性脑缺血(6小时,1 d,3 d或7 d)。通过组织学检查,免疫组织化学和原位杂交确定不同处理后HIF-1α的表达。结果HIF-1α的mRNA和蛋白表达可以在存活和坏死神经元,胶质斑层以及血管内皮细胞中检测到。缺氧预处理显着促进了局灶性脑缺血后HIF-1α的表达,尤其是缺血性外周区(P <0.05)。

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