首页> 外文期刊>Naunyn-Schmiedeberg's Archives of Pharmacology >Inhibition of TNF-α protects against hepatic ischemia-reperfusion injury in rats via NF-κB dependent pathway.
【24h】

Inhibition of TNF-α protects against hepatic ischemia-reperfusion injury in rats via NF-κB dependent pathway.

机译:TNF-α的抑制可通过NF-κB依赖性途径防止大鼠肝脏缺血再灌注损伤。

获取原文
获取原文并翻译 | 示例
           

摘要

Hepatic ischemia-reperfusion injury (I/R) is a serious health problem associated with liver transplantation, resection surgery, and various types of shock especially hemorrhagic shock. In the present investigation, the effect of inhibition of tumor necrosis factor-alpha (TNF-α) using pentoxifylline or infliximab against hepatic I/R injury induced in rats by 45-min ischemia and 1-h reperfusion was studied. It was observed that both pentoxifylline and infliximab-treated groups showed a significantly lower extent and severity of liver injury. This is attributed to (1) a decrease in oxidative stress markers, (2) reduction of the expression of TNF-α, TNF-α type-1 receptors, and nuclear factor kappa B (NF-κB). Thus TNF-α inhibition may be one of the therapeutic interventions to overcome the deleterious effects of I/R on liver via reduction of oxidative stress and inhibition of inflammatory cascade.
机译:肝缺血再灌注损伤(I / R)是与肝移植,切除手术和各种类型的休克(尤其是失血性休克)相关的严重健康问题。在本研究中,研究了使用己酮可可碱或英夫利昔单抗抑制肿瘤坏死因子-α(TNF-α)对45分钟局部缺血和1小时再灌注引起的大鼠肝脏I / R损伤的作用。观察到己酮可可碱和英夫利昔单抗治疗组均显示出肝损伤的程度和严重程度明显降低。这归因于(1)氧化应激标志物的减少,(2)TNF-α,TNF-α1型受体和核因子κB(NF-κB)的表达减少。因此,TNF-α的抑制可能是通过降低氧化应激和抑制炎症级联来克服I / R对肝脏有害作用的治疗手段之一。

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