首页> 外文期刊>Journal of International Medical Research >Effects of cyclosporin A pre-treatment combined with etomidate post-treatment on lung injury induced by limb ischemia-reperfusion in rats
【24h】

Effects of cyclosporin A pre-treatment combined with etomidate post-treatment on lung injury induced by limb ischemia-reperfusion in rats

机译:环孢菌素A预处理结合依赖于膦酸盐治疗大鼠肢体缺血再灌注肺损伤的影响

获取原文
           

摘要

Objectives To investigate the influence of cyclosporin A (CsA) pre-treatment and etomidate (ETO) post-treatment on lung injury induced by limb ischemia-reperfusion (I/R) in rats. Methods Rats were randomly divided into five groups: sham, I/R, I/R+CsA, I/R+ETO, and I/R+CsA+ETO. Limb I/R lung injury was established by bilateral clamping of the femoral arteries for 2 hours. Following reperfusion for 3 hours, blood gas analysis was performed. Pathological changes were assessed using immunohistochemistry. The apoptosis index (AI) and wet/dry weight ratio (W/D) were calculated. Levels of Fas protein and FasL mRNA were assessed by western blotting and RT-PCR, respectively. Tumor necrosis factor (TNF)-α and interleukin (IL)-1β were detected by ELISA. Results I/R resulted in decreased PaO _(2) but increased AI, W/D, Fas, FasL mRNA, TNF-α and IL-1β. Scattered punctate apoptosis and necrosis were observed by immunohistochemistry. Compared with the I/R group, the I/R+ETO and I/R+CsA groups showed increased SpO _(2), decreased AI, W/D, Fas, FasL mRNA, TNF-α and IL-1β, and decreased numbers of apoptotic and necrotic cells. Combined treatment with CsA+ETO resulted in more dramatic changes in these parameters. Conclusions ETO post-treatment and CsA pretreatment reduced lung injury induced by limb I/R in rats. The mechanism may be related to synergistic inhibition of Fas/FasL signaling.
机译:研究探讨Cycrosin A(CSA)预处理和替代(ETO)后处理对大鼠肢体缺血(I / R)诱导的肺损伤后处理的影响。方法将大鼠随机分为五组:Sham,I / R,I / R + CSA,I / R + EtO和I / R + CSA + EtO。通过双侧夹紧股骨动脉2小时的双侧夹紧建立了肢体I / R肺损伤。再灌注3小时后,进行血气分析。使用免疫组织化学评估病理学变化。计算凋亡指数(AI)和湿/干重比(W / D)。通过蛋白质印迹和RT-PCR评估Fas蛋白和FasL mRNA的水平。 ELISA检测肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1β。结果I / R导致PAO _(2)降低,但AI,W / D,FAS,FASL mRNA,TNF-α和IL-1β增加。免疫组织化学观察分散的点状细胞凋亡和坏死。与I / R组相比,I / R + eTO和I / R + CSA组显示出增加的SPO _(2),降低AI,W / D,FAS,FASL mRNA,TNF-α和IL-1β,以及减少凋亡和坏死细胞数。与CSA + ETO的组合治疗导致这些参数的更大变化。结论ETO后治疗和CSA预处理降低了大鼠肢体I / R诱导的肺损伤。该机制可以与Fas / FasL信号传导的协同抑制有关。

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