趋化因子MIP2在大鼠肝缺血/再灌注损伤后的表达
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Expression of macrophage inflammatory protein2in liver injury induced by ischemia and reperfusion in rat
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    目的研究趋化因子巨噬细胞炎性蛋白-2(MIP2)在肝缺血/再灌注损伤中(I/R)的作用。方法32只大鼠随机分为4组,每组8只。即假手术(对照)组,部分肝脏缺血90min再灌注3,9,24 h组。用RTPCR法检测肝组织中MIP2的mRNA表达,ELISA法测定血浆中MIP2蛋白表达,萘酚ASD氯醋酸盐酯酶特染技术检测肝组织内中性粒细胞浸润,并测定丙氨酸转氨酶(ALT)。结果缺血再灌注肝组织中MIP2 mRNA表达高于非缺血肝组织(P<0.01),9 h组高于3 h组(P<0.01),24 h组高于9 h组(P<0.01);MIP2血浆蛋白表达、肝内中性粒细胞浸润、ALT也与MIP2 mRNA呈一致性的变化。MIP2 mRNA表达、血浆MIP2蛋白水平与肝组织中性粒细胞浸润呈正相关,(r=0.88和0.83,P<0.01)。结论MIP2在大鼠肝缺血/再灌注损伤中作为中性粒细胞的趋化因子之一起着重要的上调作用。

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    Objective: To study the expression and effect of macrophage inflammatory protein2(MIP2) in liver injury induced by ischemia/reperfusion(I/R). Methods: Thirtytwo rats were randomly divided into 4 groups(8 rats in each group):false operation (control) group and 3, 9, 24 hours reperfusion group.The expression of MIP2 mRNA in hepatic tissue, MIP2 protein in plasma, the neutrophil infiltration in liver tissue and serum ALT were measured. Results: The expression of MIP2 mRNA in the ischemic tissue was significantly higher than that in nonischemic tissue (P<0.01), and was significantly higher in 9 hours reperfusion group than that in 3 hours reperfusion group (P<0.01); significantly higher in 24 hours reperfusion group than that in 9 hours reperfusion group (P<0.01). The level of plasma MIP2 protein, the neutrophil infiltration in liver, the degree of liver injury had the similar changs of MIP2 mRNA.The expression of MIP2 mRNA in liver ischemia tissue and the level of plasma MIP2 protein had positive correlation with neutrophil infiltration in liver tissue(P<0.01) . Conclusions :The results suggeste that MIP2, one of the neutrophil chemotactic factors, plays an important role in the liver injury induced by I/R in rats.

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梁法生,宋继昌,高英堂,张志尧, 张文,刘丽川.趋化因子MIP2在大鼠肝缺血/再灌注损伤后的表达[J].中国普通外科杂志,2004,13(2):9-106.
DOI:10.7659/j. issn.1005-6947.2004.02.009

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  • 在线发布日期: 2004-02-25