期刊文献+

高氧环境下ROS对肠上皮细胞表达TNF-α和HIF-1-α的影响 被引量:2

Influence of ROS on intestinal epithelium TNF-α and HIF-1-α during hyperoxia
下载PDF
导出
摘要 目的探讨长时间高氧治疗对机体造成严重不良反应的原因。方法用不同浓度的H_2O_2(100、200、400μM)和85%的高氧对肠上皮细胞干预24 h后,采用免疫组织化学方法检测高氧对TNF-α和HIF-1-α的影响。结果与对照组相比,高氧组和各H_2O_2组TNF-α和HIF-1-α表达水平显著增加(P<0.05),并且高氧组明显高于H_2O_2组。结论高氧环境中肠上皮细胞的损伤伴随着ROS的增加,因此认为在高氧环境中ROS对肠道损伤发挥着重要作用。 Objective To explore the reason of severe adverse effects by prolonged hyperoxia treatment.Methods The intestinal epithelium cells were treated with different concentrations of H2O2(100,200,400 μM) and 85% oxygen for 24 h.The expression levels of TNF-α and HIF-1-α were detected by immunohistochemistry.Results Compared with control group,the expression levels of TNF-α and HIF-1-α were significantly increased in hyperoxia group and H2O2 groups,and the expression levels of TNF-α and HIF-1-α were higher in hyperoxia group than those in H2O2 groups(P〈 0.05).Conclusion The injury of intestinal epithelial cells in hyperoxia environment is accompanied by ROS increase.So we make a conclusion that ROS plays an important role in intestinal injury in hyperoxia environment.
出处 《实用药物与临床》 CAS 2017年第2期121-124,共4页 Practical Pharmacy and Clinical Remedies
基金 国家自然科学基金(30871158 81170604) 辽宁省教育厅科学计划研究项目(LK201620) 盛京自由研究者基金
关键词 高氧 活性氧 过氧化氢 TNF-Α HIF-1-α Hyperoxia ROS H2O2 TNF-α HIF-1-α
  • 相关文献

参考文献2

二级参考文献30

  • 1何志义,邹朝霞,于亮,钟南山,冉丕鑫,钟小宁.红霉素对过氧化氢刺激的支气管上皮细胞表达白细胞介素-8与谷胱甘肽的影响[J].中华医学杂志,2005,85(14):976-980. 被引量:15
  • 2Kambas K,Chrysanthopoulou A,Kourtzelis I,et al.Endothelin-1 signaling promotes fibrosis in vitro in a bronchopulmonary dys- plasia model by activating the extrinsic coagulation cascade[J]. J Immunol,2011,186(11):6568-6575.
  • 3Ruiz-Pelaez JG,Charpak N.Bronchopulmonary dysplasia epi- demic:incidence and associated factors in a cohort of premature infants in Bogota,Colombia[J].Biomedica,2014,34(1):29-39.
  • 4Halliday HL,Ehrenkranz RA,Doyle LW.Early(< 8 days)postnatal corticosteroids for preventing chronic lung disease in preterm infants[J].Cochrane Database Syst Rev,2010,(1):CD001146.
  • 5Jobe AH.The new bronchopulmonary dysplasia[J].Curr Opin Pediatr,2011,23(2):167-172.
  • 6Gotfried MH.Macrolides for the treatment of chronic sinusitis,asthma,and COPD[J].Chest,2004,125(2 Suppl):52S-60S.
  • 7Sun H, Choo-Wing R, Fan J, et al. Small molecular modulation of macrophage migration inhibitory factor in the hyperoxia-in- duced mouse model of bronchopulmonary dysplasia [ J ]. Respir Res,2013,14(1) :1-11.
  • 8Slaughter JL, Stenger MR, Reagan PB, et al. Utilization of in- haled corticosteroids for infants with bronchopulmonary dyspla- sia [J]. PLoS One,2014,9(9) :e106838.
  • 9Liu Y, Qiu J, Wang Z, et al. Dimethylfumarate alleviates early brain injury and secondary cognitive deficits after experimental subarachnoid hemorrhage via activation of Keapl-Nrf2-ARE system [J]. J Neurosurg ,2015,23 ( 1 ) : 1-9.
  • 10Yam J, Frank L, Roberts RJ. Oxygen toxicity:comparison of lung biochemical responses in neonatal and adult rats [J]. Pediatr Res,1978,12(2) :115-119.

共引文献4

同被引文献4

引证文献2

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部