期刊文献+

高原地区缺血预处理对大鼠肝脏缺血再灌注的影响 被引量:2

Influence of ischemia preconditioning on hepatic ischemia-reperfusion injury of rats on plateau
下载PDF
导出
摘要 目的研究在高原地区缺血预处理对大鼠肝脏缺血再灌注的影响。方法本组99只大鼠分为IPC1组、IPC2组及PTC组。观察并统计动物术后12、24、48、72 h存活率。术后12、24、48、72 h分别开腹,取心脏血、肝脏标本进行肝功能及病理检查。比较分析三组的病理改变、死亡率及肝功能指标变化。结果 IPC2组的ALT值及死亡率均明显高于PTC组与IPC1组,IPC1组的病理改变明显轻于IPC2组,而IPC2组与PTC组的病理改变相近。结论在高原地区反复短暂的组织器官缺血可致累加性损伤,最终导致组织坏死,器官功能衰竭。 Objective To research into the effects of ischemic preconditioning(IPC) on hepatic ischemia-reperfusion injury of rats in the plateau region.Methods Totally 99 rats were divided into IPC1 group,IPC 2 group and portal trail clamp(PTC) group.The survival rate were observed and recorded at 12,24,48 and 72 h after surgery respectively.Meanwhile,the blood and tissue samples were collected to do liver function and pathological examinations.The pathological changes,motality rates and changes in liver function were compared among the three groups.Results Alanine aminotransferase(ALT) and mortality rate in IPC2 group were markedly higher than those in PTC group and IPC1 group while the pathological change was more obvious in IPC2 group than that in IPC1 group.The pathological change in PTC group was similar to that in IPC2 group.Conclusion In the plateau region,repeated transient organs ischemia will produce cumulative liver damage,ultimately leading to tissue necrosis and organ failure.
出处 《局解手术学杂志》 2011年第4期357-360,共4页 Journal of Regional Anatomy and Operative Surgery
关键词 高原地区 缺血预处理 肝脏 缺血再灌注 high altitude ischemic preconditioning liver ischemia-reperfusion
  • 相关文献

参考文献11

二级参考文献39

共引文献144

同被引文献15

  • 1Jiang H, Ma Y, Chen X, et al. Genistein synergizes with arsenic trioxide to suppress human hepatocellular carcinoma. Cancer Sci, 2010,101 (4) :975-983.
  • 2Wang D, Ma Y, Li Z, et al. The role of AKT1 and autophagy in the protective effect of hydrogen sulphide against hepatic ischemia/ reperfusion injury in mice. Autophagy ,2012,8 (6) :954-962.
  • 3Clarke C, Kuboki S, Sakai N, et al. CXC chemokine receptor-1 is expressed by hepatocytes and regulates liver recovery after hepatic ischemia/reperfusion injury. Hepatology ,2011,53 ( 1 ) :261-271.
  • 4Bamboat ZM, Ocuin LM, Balachandran VP, et al. Conventional DCs reduce liver ischemia/reperfusion injury in mice via IL-10 secretion. J Clin Invest,2010,120(2) :559-569.
  • 5Zhao ZQ, Corvera JS, Halkos ME, et al. Inhibition of myocardial injury by ischemic postconditioning during reperfusion : comparison with ische- mic preconditioning [ J ]. Am J Physiol Heart Circ Physiol, 2003,285 (2) :579 -588.
  • 6Zhang L, Ma J, Liu H. Protective effect of ischemic posteonditioning a- gainst ischemia reperfusion-induced myocardium oxidative injury in IR rats[ J 1. Molecules,2012,17 (4) :3805 - 3817.
  • 7Heusch G, Musiolik J, Gedik N, et al. Mitochondrial STAT3 activation and cardioprotection by ischemic postconditioning in pigs with regional myocardial ischemia/reperfusion [ J ]. Circ Res,2011,109 ( 11 ) : 1302 - 1308.
  • 8Bhattacharya S, Ray RM, Johnson LR, et al. STA33-mediated transcrip- tion of Bcl-2,Mcl-1 and c-IAP2 prevents apoptosis in polyamine-deple- ted cells[ J]. Biochem J,2005,392(2) :335 - 344.
  • 9Goodman MD, Koch SE, Afzal MR, et al. STAT subtype specificity and ischemic preconditioning in mice : is STAT-3 enough [ J ]. Am J Physiol Heart Cire Physio1,2011,300 ( 2 ) :522 - 526.
  • 10康凯,姜洪池,赵鸣雁,孙学英,潘尚哈.胱硫醚-γ-裂解酶/硫化氢系统在大鼠肝脏缺血再灌注损伤中的保护作用[J].中华外科杂志,2010,48(12):924-928. 被引量:10

引证文献2

二级引证文献24

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