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作 者:陈金联[1,2] 周同[1,2] 储榆德[1,2] 许蕙敏 李晓[1,2] 张明钧 张冬华[1,2] 吴云林[1,2]
机构地区:[1]上海市第六人民医院 [2]上海第二医科大学附属瑞金医院
出 处:《中国危重病急救医学》1998年第11期670-672,共3页Chinese Critical Care Medicine
摘 要:目的:探讨P选择素单克隆抗体(单抗)对大鼠肝缺血再灌注损伤的保护作用。方法:在肝缺血再灌注大鼠模型上观察了细胞间粘附分子1和P选择素的变化,并用P选择素单抗对其进行阻断治疗。结果:缺血再灌注大鼠肝细胞发生水肿及空泡变性,血清天冬氨酸转氨酶和丙氨酸转氨酶水平升高;但再灌注前5分钟经静脉注射P选择素单抗,则肝组织与正常组相近,肝细胞未见空泡变性,血清酶水平明显减低;酶联免疫吸附试验发现,再灌注后血清ICAM1和血浆P选择素水平显著升高,经P选择素单抗处理的大鼠血ICAM1和P选择素明显下降。结论:ICAM1和P选择素与缺血再灌注损伤密切相关,P选择素单抗对肝缺血再灌注损伤具有保护作用。Objective:To investigate the potential role of intercellular adhesion molecule1 ( ICAM1) and Pselectin in hepatic ischemiareperfusion injury.Methods:Using a rat model of 60minute liver ischemia followed by reperfusion,animals were divided into 3 groups:the shamoperated controls,ischemic group receiving only normal saline,and treated group receiving Pselectin monoclo nal antibody (Mab) at a dose of 2 mg/kg at 5 minutes before reperfusion.The following parameters were analyzed such as liver injury tests,liver histological examination,serum enzymes levels aspartate aminotransferase (AST),alanine aminotransferase(ALT) ,and the levels of ICAM1 and P selectin .Results:Serum AST and ALT levels were significantly increased during 60minute left lobar ischemia and reperfusion,while the increment was significantly inhibited,and liver pathology observed by light microscopy was remarkably ameliorated by treatment with Pselectin Mab.Also,the elevated levels of ICAM1 and Pselectin were found in animals after hepatic ischemiareperfusion,but they were markedly reduced in treatment group.Conclusions:ICAM1 and Pselectin may contribute to the development of hepatic ischemiareperfusion injury,and the Pselectin Mab has protective effect on acute hepatic damage induced by local ischemiareperfusion injury.
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