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出 处:《中国煤炭工业医学杂志》2013年第3期439-441,共3页Chinese Journal of Coal Industry Medicine
摘 要:目的探讨舒芬太尼对大鼠肠缺血再灌注时肝组织细胞凋亡的影响。方法成年健康Wistar大鼠24只,随机分为3组(n=8):假手术组(Sham组,S)、肠缺血再灌注组(intestine ischemical-reperfusion组,IIR)、舒芬太尼组(Sulfentanil组,SF)。通过夹闭肠系膜上动脉1h后再灌注6h制作肠缺血再灌注损伤模型,采用免疫组化法与医学图像分析检测肝组织Caspase-3蛋白表达量;TUNEL法检测肝细胞凋亡指数AI(%)。结果与S组比较,IIR组和SF组Caspase-3蛋白含量及AI均升高(P<0.05)。与IIR组比较,SF组Caspase-3蛋白含量及AI均降低(P<0.05)。结论舒芬太尼可能通过调节Caspase-3蛋白表达减轻肠缺血再灌注时肝的损伤。Objective To investigate the effects of sulfentanil on the hepatocyte apoptosis induced by intes- tinal ischemia- reperfusion in rats. Methods Twenty - four Wistar rats were randomly divided into 3 groups(n = 8) : sham - operated control group(S group) ,intestine. ischemia - reperfusion group(IIR group) and sulfentanil group(SF group). In the experiments, the root of superior mesenteric artery was blocked with non - injury artery clap for lh and reperfusion 6h. Expression of Caspase - 3 protein in liver tissues was detected with immunohistochemistry and MIAS- 2000. The apoptosis index (AI) of hepatic cell was measured by terminal deoxynucleotidy transferase mediated dUTP nick end labeling (TUNEL) method. Results Expression of Caspase- 3 protein of hepatic cell and AI in IIR group and SF group were signifi- cantly higher than in Sham group(P〈0.05). Caspase- 3 protein of hepatic cell and AI in SF group were lower than in ⅡR group(P〈0. 05). Conclusion Sulfentani 1 can relieve the liver injury by regulating Caspase- 3 protein expression.
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