首页> 外文期刊>Free radical research >Protection against in vivo liver ischemia-reperfusion injury by n-3 long-chain polyunsaturated fatty acids in the rat.
【24h】

Protection against in vivo liver ischemia-reperfusion injury by n-3 long-chain polyunsaturated fatty acids in the rat.

机译:大鼠体内n-3个长链多不饱和脂肪酸对体内肝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

N-3 polyunsaturated fatty acids (n-3 PUFA) affect inflammatory processes. This study evaluated the effects of dietary supplementation with fish oil on hepatic ischemia-reperfusion (IR) injury in the rat. Parameters of liver injury (serum transaminases and histology) and oxidative stress (serum 8-isoprostanes and hepatic GSH and GSSG), were correlated with NF-kappaB DNA binding and FA composition and inflammatory cytokine release. N-3 PUFA supplementation significantly increased liver n-3 PUFA content and decreased n-6-3 PUFA ratios. IR significantly modified liver histology and enhanced serum transaminases, 8-isoprotanes and inflammatory cytokines, with net reduction in liver GSH levels and net increment in those of GSSG. Early increase (3 h) and late reduction (20 h) in NF-kappaB activity was induced. All IR-induced changes were normalized by n-3 PUFA supplementation. In conclusion, prevention of liver IR-injury was achieved by n-3 PUFA supplementation, with suppression of oxidative stress and recovery of pro-inflammatory cytokine homeostasis and NF-kappaB functionality lost during IR.
机译:N-3多不饱和脂肪酸(n-3 PUFA)影响炎症过程。这项研究评估了膳食中添加鱼油对大鼠肝脏缺血再灌注(IR)损伤的影响。肝损伤(血清转氨酶和组织学)和氧化应激(血清8-异前列腺素和肝GSH和GSSG)的参数与NF-κBDNA结合,FA成分和炎性细胞因子释放相关。 N-3 PUFA补充剂可显着增加肝脏n-3 PUFA含量并降低n-6 / n-3 PUFA比。红外显着改变了肝脏的组织学,增强了血清转氨酶,8-异丙烷和炎性细胞因子,使肝脏GSH含量净降低,而GSSG含量净升高。诱导了NF-κB活性的早期增加(3小时)和晚期减少(20小时)。通过n-3 PUFA补充将所有IR诱导的变化归一化。总之,通过添加n-3 PUFA可以预防肝IR损伤,同时抑制氧化应激并恢复IR中丧失的促炎性细胞因子稳态和NF-κB功能。

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