{"title":"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","authors":"王娟, 张玉真, Lt, strong gt, 蒋丽忠 lt","doi":"10.3969/J.ISSN.1671-6264.2011.02.011","DOIUrl":null,"url":null,"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.","PeriodicalId":35835,"journal":{"name":"Journal of Southeast University (English Edition)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Relationship between the expression of HIF-1α and apoptosis related genes P53,Bcl-2 in cortex of hypoxia ischemia brain damage in neonatal rat\",\"authors\":\"王娟, 张玉真, Lt, strong gt, 蒋丽忠 lt\",\"doi\":\"10.3969/J.ISSN.1671-6264.2011.02.011\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":35835,\"journal\":{\"name\":\"Journal of Southeast University (English Edition)\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Southeast University (English Edition)\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3969/J.ISSN.1671-6264.2011.02.011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Southeast University (English Edition)","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3969/J.ISSN.1671-6264.2011.02.011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Engineering","Score":null,"Total":0}
Relationship between the expression of HIF-1α and apoptosis related genes P53,Bcl-2 in cortex of hypoxia ischemia brain damage in neonatal rat
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.