袁铭, 韩勇, 肖漓, 许晓光, 高钰, 钱叶勇, 石炳毅. 地奥司明对肾缺血/再灌注大鼠肾组织PECAM-1表达的影响[J]. 解放军医学院学报, 2013, 34(9): 985-988. DOI: 10.3969/j.issn.2095-5227.2013.09.027
引用本文: 袁铭, 韩勇, 肖漓, 许晓光, 高钰, 钱叶勇, 石炳毅. 地奥司明对肾缺血/再灌注大鼠肾组织PECAM-1表达的影响[J]. 解放军医学院学报, 2013, 34(9): 985-988. DOI: 10.3969/j.issn.2095-5227.2013.09.027
YUAN Ming, HAN Yong, XIAO Li, XU Xiao-guang, GAO Yu, QIAN Ye-yong, SHI Bing-yi. Effect of Diosmin on expression of PECAM-1 in kidney tissue of rats following ischemia/reperfusion injury[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2013, 34(9): 985-988. DOI: 10.3969/j.issn.2095-5227.2013.09.027
Citation: YUAN Ming, HAN Yong, XIAO Li, XU Xiao-guang, GAO Yu, QIAN Ye-yong, SHI Bing-yi. Effect of Diosmin on expression of PECAM-1 in kidney tissue of rats following ischemia/reperfusion injury[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2013, 34(9): 985-988. DOI: 10.3969/j.issn.2095-5227.2013.09.027

地奥司明对肾缺血/再灌注大鼠肾组织PECAM-1表达的影响

Effect of Diosmin on expression of PECAM-1 in kidney tissue of rats following ischemia/reperfusion injury

  • 摘要: 目的 观察地奥司明(diosmin,DOSM)对肾缺血/再灌注(ischemia/reperfusion,I/R)大鼠肾组织PECAM-1表达水平的影响,并探讨其对肾脏的保护机制。 方法 150只SD大鼠随机分成3组:假手术(sham operation,SO)组、肾缺血/再灌注模型组(I/R)和地奥司明+肾缺血/再灌注模型组(DOSM+I/R)。在再灌注不同时间点分别采用免疫组化及Western免疫印迹方法测定肾脏组织中PECAM-1的表达水平。 结果 在1 h、6 h、12 h、24 h和48 h不同时间点的肾组织中,I/R和DOSM+I/R两组PECAM-1的表达水平均随时间逐渐上调,并于48 h达最高。而在DOSM组显著低于I/R组(P<0.05或P<0.01)。Western免疫印迹与免疫组织化学检测结果基本一致。 结论 DOSM可显著降低肾I/R病理过程中PECAM-1的表达,有助于减轻I/R时炎性细胞的浸润,从而减轻缺血再灌注损伤,保护肾功能。

     

    Abstract: Objective To study the effect of diosmin (DOSM) on expression of PECAM-1 in kidney tissue of rats following ischemia/reperfusion (I/R) injury and its kidney protection mechanism. Methods One hundred and fifty SD rats were randomly divided into sham operation (SO) group, I/R group, and DOSM +I/R group. Expression level of PECAM-1 in kidney tissue was measured by immunohistochemistry and Western blot, respectively, at different time points of I/R. Results The expression level of PECAM-1 in kidney tissue increased gradually at 1, 6, 12, 24, and 48 h in I/R group and DOSM+I/R group, reached its peak at 48 h, and was significantly lower in DOSM +I/R group than in I/R group (P<0.01, P<0.05). No significant difference was found in the expression level of PECAM-1 measured by Western blot and immunohistochemistry. Conclusion DOSM can significantly downregulate the expression of PECAM-1 in rats following I/R injury and alleviate the infiltration of inflammatory cells, thus improving I/R injury and protecting renal function.

     

/

返回文章
返回