Relationship between the expression of HIF-1α and apoptosis related genes P53,Bcl-2 in cortex of hypoxia ischemia brain damage in neonatal rat

王娟, 张玉真, Lt, strong gt, 蒋丽忠 lt
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引用次数: 1

Abstract

Objective: To investigate the expression of HIF-1α and explore the relationship between expression of HIF-1α and apoptosis related genes P53,Bcl-2 in hypoxia ischemia brain damage in neonatal rats.Methods: Postnatal day 7 SD rats were divided into three groups: sham group,the hypoxia group and the hypoxia-ischemia group.Rats′ brain tissue were collected at 3,6,12,24,72 h after hypoxia or hypoxia-ischemia from each group.The histopathological damage was detected by HE staining.Immunohistochemistry was used to detect the expression of HIF-1 α,P53 and Bcl-2.Results: HE staining showed that neuronal degeneration and edema became prominent at 24 h in both hypoxia group and hypoxia-ischemia group.The expression of HIF-1 α protein was significantly upregulated at 3 h,peak at 12 h,and then decreased in both hypoxia and hypoxia-ischemia group.The expression of P53 protein was upregulated at 3 h,peak at 24 h,and then decreased in both hypoxia and hypoxia-ischemia group.The expression of Bcl-2 protein was similar with HIF-1 α in hypoxia and hypoxia-ischemia group.The ratio of P53 and Bcl-2 was almost 1 in sham group,less than 1 at 3 h,6 h,12 h,and more than 1 at 24 h and 72 h in both hypoxia and hypoxia-ischemia groups.Conclusion: The HIF-1 α participates in the regulation of P53 and Bcl-2 in hypoxia ischemia brain damage in neonatal rats.HIF-1α may have protective role in the onset of hypoxia.
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新生大鼠缺氧缺血脑损伤皮层HIF-1α与凋亡相关基因P53、Bcl-2表达的关系
目的:观察新生大鼠缺氧缺血脑损伤中HIF-1α的表达,探讨HIF-1α与凋亡相关基因P53、Bcl-2表达的关系。方法:将出生后第7天SD大鼠分为假手术组、缺氧组和缺氧缺血组。分别于缺氧或缺氧缺血后3、6、12、24、72 h采集各组大鼠脑组织。HE染色检测组织病理损伤。免疫组化检测HIF-1 α、P53、Bcl-2的表达。结果:HE染色显示,缺氧组和缺氧缺血组在24 h均出现明显的神经元变性和水肿。缺氧组和缺氧缺血组HIF-1 α蛋白表达在3 h时显著上调,12 h时达到峰值,缺氧组和缺氧缺血组HIF-1 α蛋白表达均呈下降趋势。在缺氧组和缺氧缺血组中,P53蛋白的表达在3 h时上调,24 h时达到峰值,然后下降。缺氧组和缺氧缺血组Bcl-2蛋白表达与HIF-1 α相似。假手术组P53与Bcl-2的比值几乎为1,缺氧组和缺氧缺血组在3、6、12 h时均小于1,在24、72 h时均大于1。结论:HIF-1 α参与了新生大鼠缺氧缺血脑损伤中P53和Bcl-2的调控。HIF-1α可能在缺氧发生过程中具有保护作用。
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