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作 者:王旭锋[1] 曹农[1] 柴琛[1] 鲁彦[2] 李鑫[1] 张鹏[1] 徐松[1]
机构地区:[1]兰州大学第一医院普外一科,甘肃兰州730000 [2]解放军第一医院检验科,甘肃兰州730030
出 处:《中国急救医学》2013年第10期869-872,I0001,共5页Chinese Journal of Critical Care Medicine
基 金:国家863计划项目(2011AA02A111)
摘 要:目的 采用盲肠结扎穿孔术复制大鼠脓毒症模型,研究糖蛋白(glycoprotein,GP)Ⅱb/Ⅲa受体抑制剂依替巴肽(Eptifibatide)对脓毒症大鼠急性肺损伤的保护作用.方法 64只雄性SD大鼠随机分为三组:假手术组16只、盲肠结扎穿孔(cecal ligation and puncture,CLP)组和治疗组各24只,每组再均分为6 h、10 h、14 h和18 h四个亚组(假手术组每个亚组均4只,CLP组和治疗组各亚组均6只),其中治疗组术后4 h、8 h、12 h和16 h经大鼠尾静脉给予依替巴肽(7.5 mg/kg)干预.术后间隔不同的时间后将大鼠放血活杀,取出待测肺组织,检测肺微血管通透性改变、肺湿/干质量(W/D)比值,进行肺组织形态学观察和病理评分,并检测肺微血管内皮细胞的凋亡情况.结果 CLP组大鼠肺组织6 h开始出现损伤,10 h、14 h和18 h损伤逐渐加重,损伤在CLP后18 h最重;与CLP组比较,治疗组各时间点大鼠肺微血管通透性明显降低(P〈0.05),致使肺组织W/D值亦明显降低(P〈0.05),肺组织炎细胞浸润、水肿、出血等损伤表现减轻,肺组织病理评分明显降低(P〈0.05);治疗组术后各观察时间点肺微血管内皮细胞的凋亡率明显降低,与CLP组比较差异均有统计学意义(P〈0.05).结论 GP Ⅱb/Ⅲa受体抑制剂依替巴肽对脓毒症大鼠急性肺损伤有保护作用.Objective To investigate the effects of Glycoprotein Ⅱ b/Ⅲ a receptor inhibitors eptifibatide against acute lung injury in rat septic models. Methods 64 SD male rats were randomly divided into three groups: sham operation, cecal ligation and puncture (CLP) and treatment group. Each group was divided into four sub -groups: 6 h, 10 h, 14 h and 18 h after operation (four rats in each sham sub - groups, six rats in each CLP and treatment sub - groups). In treatment group, rats were treated with eptifibatide (7. 5 mg/kg) at g h, 8 h, 12 h and 16 h. The permeability of microvasculature, water contents, pathological tissue scores and the apoptosis of microvascular endothelial cells in lung microvasculature were examined at 6 h, 10 h, 14 h and 18h after operation. Results The rat lung injury happened as early as 6 h of CLP operation ; and became worse as time went on(10 h,lg h and 18 h) ; the damage was most serious in 18 h of CLP operation. Compared with CLP group, pulmonary microvascular protein leak, as assessed by Evans blue dye, was significantly reduced in treatment groups ( P 〈 0.05 ) ; and the pulmonary wet/dry weight ratio was lower ( P 〈 0.05 ), the pathological tissue scores was markedly decreased ( P 〈 0.05 ) in treatment group ; the apoptosis of lung microvascular endothelial cells in treatment group at 6 h, 10 h, 14 h and 18 h were significantly decreased compared with the CLP group ( P 〈 0.05 ). Conclusion Glycoprotein H b/Ill a receptor inhibitors eptifibatide could protect rat from acute lung injury induced by sepsis. [Key words] Sepsis; Acute lung injury(ALI) ; Eptifibatide; GPⅡb/Ⅲa; Apoptosis decreased compared with the CLP group ( P 〈 0.05 ). Conclusion Glycoprotein Ⅱb/Ⅲa receptor inhibitors eptifibatide could protect rat from acute lung injury induced by sepsis.
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