首页> 外文会议>International Society for Free Radical Research >Cytoprotective Effect of Vitamin E Against D-Galactosamine-Induced Cell Death Is More Related to Transcriptional than Antioxidant Regulatory Properties in Cultured Human Hepatocytes
【24h】

Cytoprotective Effect of Vitamin E Against D-Galactosamine-Induced Cell Death Is More Related to Transcriptional than Antioxidant Regulatory Properties in Cultured Human Hepatocytes

机译:维生素E对D-半乳糖胺诱导的细胞死亡的细胞保护作用与培养的人肝细胞中的抗氧化调节性能有关

获取原文

摘要

The aim of the present study was to determine if the regulation of oxidative stress by vitamin E is related to its cytoprotective properties against D-GalN-in-duced cell death in cultured human hepatocytes. Liver samples were obtained from surgery of hepatic tumors, Vitamin E (50 |J.M) was added 10 h after D-GalN (40 mM), D-GalN induced oxidative stress, apoptosis and necrosis in cultured human hepatocytes. This citotoxic effect of D-GalN was associated with a raise of inducible nitric oxide synthase (NOS-2), CYP3A4 and CYP3A5, but reduced PPAR-a, PXR and CPT1-A expression Vitamin E reduced D-GalN-induced cell death without modification of intracellular oxidative stress,. Vitamin E reduced NF-kappaB activation and NOS-2, but increased CYP3A4, CYP3A5, PPAR-a, PXR and CPT1-A expression in D-GalN-treated hepatocytes.
机译:本研究的目的是确定维生素E的氧化应激的调节是否与其在培养的人肝细胞中对D-Galn-in-Lib-in-in-Deacter死亡的细胞保护性能有关。肝脏样品从肝脏肿瘤的手术中获得,在D-Galn(40mm)后加入10小时,D-Galn诱导培养的人肝细胞中的氧化应激,细胞凋亡和坏死。这种D-GALN的胞虫毒性效应与诱导型一氧化氮合酶(NOS-2),CYP3A4和CYP3A5的升高相关,但是降低了PPAR-A,PXR和CPT1-A表达维生素E,减少了D-Galn诱导的细胞死亡细胞内氧化应激的改性。维生素E降低了NF-κB活化和NOS-2,但CYP3A4,CYP3A5,PPAR-A,PXR和CPT1-A的表达增加,CYP3A4,CPP,PPAR-A,PXR和CPT1-A表达。

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