Relationship between the expression of HIF-1α and apoptosis related genes P53,Bcl-2 in cortex of hypoxia ischemia brain damage in neonatal rat
Jiang Li
Abstract
Jiang Li
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.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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.
Key concepts: Hypoxia (environmental), Ischemia, Apoptosis, Immunohistochemistry, Downregulation and upregulation, Endocrinology, Internal medicine, Brain damage