大鼠局灶性脑缺血再灌注后凋亡分子C/EBP同源蛋白的表达变化
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The Expression Development of Proapoptic Molecule C/EBP Homology Protein mRNA and Protein Following Focal Cerebral schemia/Reperfusion in Rats
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    摘要:

    目的观察大鼠脑缺血再灌注后凋亡分子C/EBP同源蛋白的表达变化,探讨该分子对神经细胞凋亡的影响。 方法制备SD大鼠大脑中动脉闭塞模型,逆转录聚合酶链反应法、免疫组织化学染色分别测定大鼠脑缺血半暗带区再灌注后不同时相C/EBP同源蛋白 mRNA及蛋白的表达变化;缺口末端标记法测定神经细胞凋亡。结果模型组C/EBP同源蛋白 mRNA表达于再灌注后12 h达高峰,其蛋白表达于再灌注后24 h达高峰,与神经细胞凋亡变化趋势相平行。结论大鼠脑缺血再灌注可诱导C/EBP同源蛋白表达,C/EBP同源蛋白在缺血再灌注所致神经细胞凋亡中可能发挥重要作用。

    Abstract:

    AimTo detect the expression development of proapoptic molecule C/EBP homology protein(CHOP) mRNA and protein, and explore its effect on neuronal apoptosis after cerebral ischemia/reperfusion in rats.MethodsTransient focal cerebral ischemia was induced by middle cerebral artery occlusion (MCAO) for 2 hours followed by reperfusion in sprague-dawley rats.Then,the expression of CHOP protein and/or mRNA were measured with methods of immunohistochemistry and reverse transcription-polymerase chain reaction (RT-PCR) at 1 h, 3 h, 6 h, 12 h and 24 h after reperfusion in cerebral cortex of rats.The neuronal apoptosis was detected by the method of terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL).ResultsIn cerebral ischemia model group,the expression level of CHOP mRNA reached a peak at 12 h after reperfusion and that of CHOP protein reached a peak at 24 h after reperfusion,which paralleled with the tendency of neuronal apoptosis development.ConclusionCerebral ischemia reperfusion may induce CHOP expression. CHOP may play an important role in neuronal apoptosis induced by cerebral ischemia/reperfusion.

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申向民,杨期东,谭利明,刘运海,唐震宇,黄清,周琳.大鼠局灶性脑缺血再灌注后凋亡分子C/EBP同源蛋白的表达变化[J].中国动脉硬化杂志,2010,18(1):43~46.

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  • 收稿日期:2009-09-28
  • 最后修改日期:2010-01-05
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