2007Journal of Shandong UniversityRequires access

Ischemia preconditioning reduces ischemia/reperfusion injury of the hippocampal neurons by inhibiting the release of cytochrome c from mitochondria in rats

Lian-Bi Chen

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Abstract

Objective:To investigate the role of the release of cytochrome c from mitochondria in the protective process of hippocampal neurons against ischemia/reperfusion injury by cerebral ischemic preconditioning(IPC) in rats.Methods: Rats were randomly divided into three groups: an ischemia/reperfusion group(IR),an ischemic preconditioning+ischemia/reperfusion group(IPC+IR),and the control group.Histological changes in the neurons of the hippocampal CA1 region were obtained by HE staining.The apoptotic neurons were counted with TUNEL staining and the release of cytochrome c from the mitochondria were determined with immunohistochemistry in the same brain area.Results: Compared with the IR group,cerebral ischemic preconditioning can increase the number of surviving neurons in the hippocampal CA1 region(P0.001),markedly reduce the number of apoptotic pyramidal neurons(P0.001),and inhibit the release of cytochrome c from mitochondria.Conclusion: Cerebral ischemic preconditioning(IPC) can protect the hippocampal neurons against ischemia/reperfusion injury by reducing the release of cytochrome c from mitochondria and inhibiting the apoptosis.

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Objective:To investigate the role of the release of cytochrome c from mitochondria in the protective process of hippocampal neurons against ischemia/reperfusion injury by cerebral ischemic preconditioning(IPC) in rats.Methods: Rats were randomly divided into three groups: an ischemia/reperfusion group(IR),an ischemic preconditioning+ischemia/reperfusion group(IPC+IR),and the control group.Histological changes in the neurons of the hippocampal CA1 region were obtained by HE staining.The apoptotic neurons were counted with TUNEL staining and the release of cytochrome c from the mitochondria were determined with immunohistochemistry in the same brain area.Results: Compared with the IR group,cerebral ischemic preconditioning can increase the number of surviving neurons in the hippocampal CA1 region(P0.001),markedly reduce the number of apoptotic pyramidal neurons(P0.001),and inhibit the release of cytochrome c from mitochondria.Conclusion: Cerebral ischemic preconditioning(IPC) can protect the hippocampal neurons against ischemia/reperfusion injury by reducing the release of cytochrome c from mitochondria and inhibiting the apoptosis.

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Available abstract

Objective:To investigate the role of the release of cytochrome c from mitochondria in the protective process of hippocampal neurons against ischemia/reperfusion injury by cerebral ischemic preconditioning(IPC) in rats.Methods: Rats were randomly divided into three groups: an ischemia/reperfusion group(IR),an ischemic preconditioning+ischemia/reperfusion group(IPC+IR),and the control group.Histological changes in the neurons of the hippocampal CA1 region were obtained by HE staining.The apoptotic neurons were counted with TUNEL staining and the release of cytochrome c from the mitochondria were determined with immunohistochemistry in the same brain area.Results: Compared with the IR group,cerebral ischemic preconditioning can increase the number of surviving neurons in the hippocampal CA1 region(P0.001),markedly reduce the number of apoptotic pyramidal neurons(P0.001),and inhibit the release of cytochrome c from mitochondria.Conclusion: Cerebral ischemic preconditioning(IPC) can protect the hippocampal neurons against ischemia/reperfusion injury by reducing the release of cytochrome c from mitochondria and inhibiting the apoptosis.

Key concepts: Hippocampal formation, Cytochrome c, TUNEL assay, Ischemia, Ischemic preconditioning, Mitochondrion, Apoptosis, Reperfusion injury

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