...
首页> 外文期刊>Transplantation Proceedings >Down-regulation of cyclooxygenase-2 is involved in ischemic postconditioning protection against renal ischemia reperfusion injury in rats.
【24h】

Down-regulation of cyclooxygenase-2 is involved in ischemic postconditioning protection against renal ischemia reperfusion injury in rats.

机译:环氧合酶2的下调参与缺血后处理对大鼠肾脏缺血再灌注损伤的保护作用。

获取原文
获取原文并翻译 | 示例
           

摘要

Ischemic postconditioning (IPostC) is a phenomenon whereby rapid intermittent interruptions of blood flow in the early phase of reperfusion protect an organ from ischemia-reperfusion injury. In the present study, we investigated whether the protective effect of IPostC was associated with the cyclooxygenase-2 (COX-2) pathway by evaluating its expression following renal ischemia-reperfusion in rats. Animals underwent 45 minutes of renal pedicle occlusion followed by reperfusion for 1.5, 3, 6, 12, or 24 hours. IPostC was performed by six 10-second cycles of reperfusion and 10 seconds of renal pedicle occlusion at the end of ischemia. Blood and kidney samples were collected at each reperfusion time point. The protein expression of COX-1 and COX-2 were evaluated by Western blotting. Our data showed that IPostC attenuated the renal dysfunction and decreased COX-2 expression induced by ischemia-reperfusion insults. The results indicated that the protective effect of IPostC was related to down-regulation of COX-2 expression.
机译:缺血后处理(IPostC)是一种现象,在再灌注的早期阶段,快速的间歇性血流中断可以保护器官免受缺血-再灌注损伤。在本研究中,我们通过评估大鼠肾脏缺血再灌注后的表达来研究IPostC的保护作用是否与环氧合酶2(COX-2)通路相关。对动物进行45分钟的肾蒂阻塞,然后再灌注1.5、3、6、12或24小时。在局部缺血结束时,通过六个10秒的再灌注周期和10秒的肾蒂阻塞,进行IPostC。在每个再灌注时间点采集血液和肾脏样本。通过蛋白质印迹法评估COX-1和COX-2的蛋白表达。我们的数据显示,IPostC可减轻缺血再灌注损伤所致的肾功能不全并降低COX-2表达。结果表明,IPostC的保护作用与COX-2表达的下调有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号