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晚期缺血预适应促进低氧诱导因子的表达,减轻肾脏缺血再灌注损伤 被引量:10

Protective effect of delayed ischemic preconditioning on renal ischemia/reperfusion injury via induction of hypoxia inducible factor
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摘要 目的:探讨晚期缺血预适应对肾脏缺血再灌注损伤的作用,以及低氧诱导因子1α(HIF-1α)在其中的作用。方法:将雄性C57/BL6N小鼠随机分为3组:假手术组(sham)、缺血再灌注组(IR)和缺血预适应组(IPC)。采用夹闭双侧肾蒂30 min后恢复灌注的方法建立肾缺血再灌注小鼠模型;缺血预适应组4 d前给予肾脏15 min预缺血。观察缺血预处理对再灌注后不同时点血肌酐(Scr)、尿素氮(BUN)、肾组织形态学和细胞凋亡的影响。采用免疫组化及Western印迹法,分析HIF-1α在肾组织的表达;采用实时定量RT-PCR法,检测血管内皮生长因子(VEGF)和葡萄糖转运子-1(Glut-1)的mRNA表达。结果:再灌注24 h后,IPC组小管间质损伤程度较IR组显著减轻,Scr、BUN水平以及小管上皮细胞凋亡明显下降。IPC组的HIF-1α核内表达显著高于IR组,且HIF-1下游靶基因VEGF和Glut-1的mRNA表达亦显著增加。结论:晚期缺血预适应能够显著改善缺血再灌注后肾脏的形态和功能,这种保护作用可能与促进低氧诱导因子高表达有关。 AIM : To investigate the effects of delayed ischemic preconditioning on renal ischemia - reperfusion injury in mice and to study the role of hypoxia inducible factor let( HIF -lot). METHODS: Male C57/BL6N mice were randomly divided into 3 groups : sham operation group ( sham), ischemia/reperfusion group (IR) and ischemic precondi- tioning group(IPC). Thirty-minute ischemia was induced by clamping renal bilateral pedicles followed by reperfusion in IR group. Fifteen -minute pre - ischemia was performed 4 days before IR in IPC group. Serum creatinine(Scr), blood urea nitrogen( BUN), kidney morphology and apoptosis were observed at different time points following reperfusion. The expression of HIF - 1 α in the renal tissues was evaluated by the methods of immunohistochemistry and Western blotting analysis. The mRNA expression of vascular endothelial growth factor(VEGF) and glucose transporter - 1 (Glut - 1 ) was detected by real - time quantitative RT - PCR. RESULTS: Compared with IR group at 24 h following reperfusion, acute tubu- lointerstitial injury was significantly relieved in IPC group. The levels of Scr and BUN, and apoptosis of tubular epithelial cells were also decreased in IPC group. Nuclear expression of HIF - 1 α was higher in IPC group than that in IR group. The mRNA expression of VEGF and Glut - 1, the target genes of HIF - 1, was also increased significantly in IPC group. CON- CLUSION: Delayed ischemic preconditioning attenuates both morphologic and functional injuries induced by renal ischemia/reperfusion. This protective effect may be related to the increased expression of hypoxia inducible factor.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2011年第2期320-325,共6页 Chinese Journal of Pathophysiology
基金 国家自然科学基金资助项目(No.30871176 No.30971374)
关键词 缺血预处理 缺血再灌注 低氧诱导因子 Kidney Ischemic preconditioning Ischemia- reperfusion Hypoxia-inducible factor
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参考文献13

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二级参考文献23

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共引文献14

同被引文献82

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