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首页> 外文期刊>Cryobiology: International Journal of Low Temperature Biology and Medicine >Marked difference in tumor necrosis factor-alpha expression in warm ischemia- and cold ischemia-reperfusion of the rat liver.
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Marked difference in tumor necrosis factor-alpha expression in warm ischemia- and cold ischemia-reperfusion of the rat liver.

机译:大鼠肝脏热缺血和冷缺血再灌注中肿瘤坏死因子-α表达的明显差异。

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Although tumor necrosis factor-alpha has been implicated in liver injury after both warm ischemia- and cold ischemia-reperfusion, it is unclear whether reactivity of the liver to these stimuli is similar with regard to cytokine expression. Here we compare the effects of warm and cold ischemia on tumor necrosis factor-alpha expression and test the hypothesis that cold ischemia preceding warm ischemia causes overexpression of this cytokine. Rat livers were flushed out with University of Wisconsin solution and subjected to varying periods of warm ischemia, cold ischemia, or cold ischemia plus warm ischemia followed by reperfusion using a blood-free perfusion model. Tumor necrosis factor-alpha and interleukin-10 release into the perfusate and bile were measured by ELISA, and expression of these cytokines and that of c-fos, c-jun, and c-myc were studied by reverse-transcriptase polymerase chain reaction. We found high levels of tumor necrosis factor-alpha in the perfusates of livers subjected to warm ischemia-reperfusion, whereas minimal or no tumor necrosis factor-alpha was detected in livers subjected to cold ischemia-reperfusion or to cold ischemia plus warm ischemia-reperfusion. Reverse-transcriptase polymerase chain reaction confirmed the above findings and showed that immediate early genes were expressed in reperfused groups of livers. Measurements of cytokine release into bile showed that neither tumor necrosis factor-alpha nor interleukin-10 were upregulated by cold ischemia-reperfusion. The results suggest that (1) warm ischemia- and cold ischemia-reperfusion of rat liver lead to very different outcomes with regard to tumor necrosis factor-alpha expression and (2) cold ischemia preceding warm ischemia prevents upregulation of tumor necrosis factor-alpha. Copyright 2000 Academic Press.
机译:尽管肿瘤坏死因子-α与热缺血和冷缺血-再灌注后的肝损伤有关,但尚不清楚肝对这些刺激的反应性在细胞因子表达方面是否相似。在这里,我们比较了热缺血和冷缺血对肿瘤坏死因子-α表达的影响,并检验了在热缺血之前冷缺血导致该细胞因子过度表达的假说。用威斯康星大学溶液冲洗大鼠肝脏,并经历不同时期的热缺血,冷缺血或冷缺血加热缺血,然后使用无血灌注模型进行再灌注。通过ELISA测定肿瘤坏死因子-α和白介素-10释放到灌注液和胆汁中,并通过逆转录酶聚合酶链反应研究这些细胞因子以及c-fos,c-jun和c-myc的表达。我们发现在经历热缺血-再灌注的肝脏灌注液中高水平的肿瘤坏死因子-α,而在经历过冷缺血-再灌注或经历冷缺血加温缺血-再灌注的肝脏中检测到极少或没有肿瘤坏死因子-α 。逆转录酶聚合酶链反应证实了上述发现,并表明立即早期基因在肝脏的再灌注组中表达。细胞因子释放入胆汁的测量表明,冷缺血-再灌注均未上调肿瘤坏死因子-α和白介素-10。结果表明,(1)大鼠肝脏的热缺血-和冷缺血-再灌注导致关于肿瘤坏死因子-α表达的不同结果;(2)温暖缺血之前的冷缺血阻止了肿瘤坏死因子-α的上调。版权所有2000学术出版社。

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