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缺血预处理对大鼠移植肝脏缺血再灌注损伤的保护作用
引用本文:涂兵,严律南,刘智敏.缺血预处理对大鼠移植肝脏缺血再灌注损伤的保护作用[J].中国普外基础与临床杂志,2002,9(2):89-92.
作者姓名:涂兵  严律南  刘智敏
作者单位:四川大学华西医院普外科,成都,610041
摘    要:目的 探讨缺血预处理 (ischemicpreconditioning ,IP)对大鼠移植肝脏缺血再灌注损伤的保护作用。 方法 采用SD大鼠原位肝移植动物模型 ,供肝冷保存时间 10 0min ,无肝期 2 5min。 64只SD大鼠随机均分成两组 :对照组 ,获取供肝前仅以肝素生理盐水经门静脉灌注 ;IP组 ,获取供肝前阻断肝门血供 10min ,再灌注 10min ,然后再以肝素生理盐水经门静脉灌注。每组受体的一半 (n =8)用于观察存活率 ,另一半 (n =8)用于移植肝脏再灌注 2h后取血及肝脏检测。结果 IP组的 1w存活率、胆汁分泌量、抗氧化酶活力、血清NO水平均明显高于对照组 (P<0 .0 5 ) ,血清ALT、AST、LDH、TNF及肝组织中的过氧化产物含量均明显低于对照组 (P<0 .0 5 ) ,组织的病理改变也轻于对照组。结论 IP能够提高血清NO水平 ,降低血清TNF含量 ,对大鼠移植肝脏的缺血再灌注损伤具有保护作用

关 键 词:缺血预处理  大鼠  移植肝脏  缺血再灌注损伤
文章编号:1007-9424(2002)02-0089-04
修稿时间:2001年7月11日

Protective Effect of Ischemic Preconditioning on Ischemic-Reperfusion Injury of Rat Liver Graft
Abstract:Objective To investigate the protective effect of ischemic preconditioning (IP) on ischemic reperfusion injury of rat liver graft. Methods Male Sprague Dawley rats were used as donors and recipients of orthotopic liver transplantation,the period of cold preservation and anhepatic phase were 100 min and 25 min respectively.Sixty four rats were randomly divided into 2 groups ( n =32),control group: donor livers were flushed through the portal veins with physiological saline solution containing heparin only before harvested; IP group: before donor livers were harvested,the portal veins and hepatic arteries of them were interrupted for 10 min,and reflow was initiated for another 10 min,then did as control group.One half of each group were used to investigate 1 week survival rate of recipients,and another half of each group were used to take sample of blood and hepatic tissue after 2 hours of reperfusion of liver graft. Results One week survival rate,amount of bile,serum NO and activity of anti oxidase were higher in IP group than those in control group( P <0.05),meanwhile,serum ALT,AST,LDH,TNF and superoxide in hepatic tissue were lower in IP group than those in control group ( P <0.05),and histological findings in IP group showed less injury than those in control group. Conclusion IP could increase production of serum NO,reduce the level of serum TNF and protect rat liver graft from ischemic reperfusion injury.
Keywords:Ischemic preconditioning    Rat  Liver graft    Ischemic  reperfusion injury  
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