缺血预处理和后适应对大鼠肝脏热缺血再灌注后HIF-1α、VEGF和TGF-β表达的影响

Anders R Knudsen, Anne-Sofie Kannerup, Henning Grønbæk, Kasper J Andersen, Peter Funch-Jensen, Jan Frystyk, Allan Flyvbjerg, Frank V Mortensen
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引用次数: 27

摘要

背景:缺血预处理和后适应可保护肝脏免受缺血/再灌注损伤。本研究旨在探讨缺血前适应和后适应对肝组织缺氧诱导因子1α (HIF-1α)、血管内皮生长因子A (VEGF-A)和转化生长因子β (TGF-β)基因表达的影响。方法:28只大鼠随机分为5组:对照组;缺血/再灌注;缺血预处理(IPC);缺血后适应(IPO);IPC和IPO的结合。IPC分为缺血10 min和再灌注10 min。IPO包括30秒再灌注和30秒缺血三个周期。结果:肝缺血后HIF-1α mRNA表达明显高于对照组(p = 0.010)。与缺血再灌注组相比,缺血再灌注组或缺血再灌注组HIF-1α mRNA表达明显降低(p = 0.002)。与对照组相比,缺血/再灌注组或IPC与IPO联合组VEGF-A mRNA表达升高(p < 0.05)。结论:缺血条件反射可能阻止大鼠肝脏缺血再灌注后HIF-1α mRNA的诱导。这表明缺血调节的保护作用不涉及HIF-1系统。另一方面,HIF-1α反应的大小可能是肝缺血后I/R损伤程度的一个标志。需要进一步的研究来澄清这个问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effects of ischemic pre- and postconditioning on HIF-1α, VEGF and TGF-β expression after warm ischemia and reperfusion in the rat liver.

Background: Ischemic pre- and postconditioning protects the liver against ischemia/reperfusion injuries. The aim of the present study was to examine how ischemic pre- and postconditioning affects gene expression of hypoxia inducible factor 1α (HIF-1α), vascular endothelial growth factor A (VEGF-A) and transforming growth factor β (TGF-β) in liver tissue.

Methods: 28 rats were randomized into five groups: control; ischemia/reperfusion; ischemic preconditioning (IPC); ischemic postconditioning (IPO); combined IPC and IPO. IPC consisted of 10 min of ischemia and 10 min of reperfusion. IPO consisted of three cycles of 30 sec. reperfusion and 30 sec. of ischemia.

Results: HIF-1α mRNA expression was significantly increased after liver ischemia compared to controls (p = 0.010). HIF-1α mRNA expression was significantly lower in groups subjected to IPC or combined IPC and IPO when compared to the ischemia/reperfusion group (p = 0.002). VEGF-A mRNA expression increased in the ischemia/reperfusion or combined IPC and IPO groups when compared to the control group (p < 0.05).

Conclusion: Ischemic conditioning seems to prevent HIF-1α mRNA induction in the rat liver after ischemia and reperfusion. This suggests that the protective effects of ischemic conditioning do not involve the HIF-1 system. On the other hand, the magnitude of the HIF-1α response might be a marker for the degree of I/R injuries after liver ischemia. Further studies are needed to clarify this issue.

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