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机构地区:[1]中山医科大学病理学教研室,510089 [2]中山医科大学附属第一医院器官移植中心,510080
出 处:《广州医药》2000年第4期3-4,共2页Guangzhou Medical Journal
摘 要:目的:探讨 ICAM-1/LFA-1分子表达与大鼠肝脏缺血再灌注损伤的关系。方法:将40只实验大鼠分为两组,分别阻断左叶及中叶肝脏的门静脉分支 30 min和 60min。所有大鼠在去阻断血流48 h后杀死,取肝组织做冰冻及石蜡切片,进行免疫组化分析及组织学观察。结果:在阻断血流 30 min的实验组中,未见明显的肝组织学损伤,肝组织内 ICAM-1及LFA-1仅有微弱表达,而在阻断血流 60 min的实验组中,肝组织损伤严重,肝组织内ICAM-1和LFA-1的表达明显增强。结论:肝组织内ICAM-1和LFA-1的表达水平与肝脏缺血再灌注损伤的程度密切相关。Objective: To investigate the relationship between the expression of intercellular adhesionmolecule-l/lymPhocyte function-associated antigen-l and rat liver ischemia-reperfusion injury. Meth-ods: Forty adult Wistar rats were randomized into 2 groups. The hepatic hilar Vessels distributing to the leftand median lobes were clamped for 30 min and 60 min respectively. All rats were killed 48 h after declamp-ing and specimens of liver tissue were obtained. Frozen and paraffin sections were analyzed through immuno-histochemistry and histology. Results: In the 30 min group, no evident histological liver in jnjury was found.The expression of ICAM-l and LFA-l on liver tissue was delicate. However, after 60 min warm ischem-a, reperfusion induced severe liver damages. The eXpression of ICAM -l and LFA-l was also notable.Conclusion: The expression level of ICAM-l and LFA-l is closely associated with the degree of liver is-chemia-reperfusion injury.
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