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Role of NF-kappaB in Liver Ischemia Reperfusion Injury of Rats

机译:NF-κB在大鼠肝缺血再灌注损伤中的作用

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摘要

To determine the role of NF-kappaB in ischemia reperfusion (I/R) injury of the rat liver, rats underwent partial hepatic ischemia and reperfusion. The left and median lobes of the liver were subjected to ischemia for 90 min followed by reperfusion for defined times. NF-kappaB activity was analyzed by electrophoretic mobility shift assay (EMSA). Semiquantitative reverse-transcriptase polymerase chain reaction was used to analyze TNF-α and ICAM-1 mRNA levels. Results showed during liver I/R injury, NF-kappaB activation was induced in a time dependent manner. NF-kappaB was activated within 1 h and 2 h after the initiation of reperfusion and decreased after 4 h. Messenger RNA expression of TNF-α and ICAM-1 were increased after the reperfusion of 2 h. It was concluded that during hepatic I/R injury, NF-kappaB was activated and could bind to special sequence in the promoters of budget genes, which can up-regulate the expression of TNF-α and ICAM-1 mRNA to result in ischemia reperfusion injury of the rat liver.
机译:为了确定NF-κB在大鼠肝脏缺血再灌注(I / R)损伤中的作用,对大鼠进行了部分肝缺血和再灌注。对肝脏的左叶和中叶进行缺血90分钟,然后再灌注规定的时间。通过电泳迁移率变动分析(EMSA)分析NF-κB活性。使用半定量逆转录酶聚合酶链反应分析TNF-α和ICAM-1 mRNA水平。结果显示,在肝I / R损伤期间,以时间依赖性方式诱导NF-κB活化。 NF-κB在再灌注开始后1小时和2小时内被激活,并在4小时后降低。再灌注2 h后TNF-α和ICAM-1的Messenger RNA表达增加。结论:肝I / R损伤过程中,NF-κB被激活并与预算基因启动子的特殊序列结合,从而上调TNF-α和ICAM-1 mRNA的表达,导致缺血再灌注。大鼠肝脏损伤。

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