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依达拉奉联合灯盏花素对脑缺血大鼠大脑皮质MCP-1的影响
引用本文:李璠,陈伟伟,赵晓姝,曾洪艳,韩宏,宋咏丽,袁云,吴春云.依达拉奉联合灯盏花素对脑缺血大鼠大脑皮质MCP-1的影响[J].中国临床解剖学杂志,2018,36(1):38-44.
作者姓名:李璠  陈伟伟  赵晓姝  曾洪艳  韩宏  宋咏丽  袁云  吴春云
作者单位:1.昆明医科大学科研实验中心; 2. 昆明医科大学人体解剖学与组织胚胎学系, 昆明 650500;
3. 昆明医科大学海源学院, 昆明 651701
基金项目:云省应用基础研究计划重点项目(2015FA020);国家自然科学基金(31260254)
摘    要:目的 观察大鼠脑缺血(MCAO)后大脑皮质MCP-1的表达变化以及用依达拉奉联合灯盏花素干预后对MCP-1表达的影响。 方法 复制大鼠大脑中动脉闭塞(MCAO)模型,应用RT-PCR、Western blot和免疫荧光技术检测大鼠MCAO及药物干预后MCP-1的表达变化。 结果 RT-PCR显示大鼠MCAO后大脑皮质MCP-1 mRNA的表达比对照组显著上升(P<0.05),12 h达高峰,与1 d、3 d及1周组比有显著差异(P<0.05);给予两种药物联合处理后,mRNA表达显著降低,与对照组及单独用药组相比均有显著差异(P<0.05)。 Western blot显示MCAO 1 d、3 d、1周大脑皮质MCP-1蛋白的表达显著增强,与对照组比有显著差异(P<0.05);两种药物联合处理后,MCAO大鼠大脑皮质MCP-1蛋白表达明显减少,与对照组及单独用药相比均有显著差异(P<0.05)。免疫荧光染色显示MCAO大鼠缺血半暗带有大量激活小胶质细胞,一部分与MCP-1免疫阳性细胞有共表达,其中MCAO后1周组最明显。 结论 大鼠局灶性脑缺血(MCAO)后,依达拉奉联合灯盏花素治疗能有效减少大脑皮质MCP-1的表达,效果优于两种药物单独使用。

关 键 词:脑缺血    灯盏花素    依达拉奉    MCP-1    大鼠   
收稿时间:2017-09-13

The effects of edaravone combined with breviscapine treatment on MCP-1 expression in the cerebral cortex after focal cerebral ischemia in rats
LI Fan,CHEN Wei-wei,ZHAO Xiao-shu,ZENG Hong-yan,HAN Hong,SONG Yong-li,YUAN Yun,WU Chun-yun.The effects of edaravone combined with breviscapine treatment on MCP-1 expression in the cerebral cortex after focal cerebral ischemia in rats[J].Chinese Journal of Clinical Anatomy,2018,36(1):38-44.
Authors:LI Fan  CHEN Wei-wei  ZHAO Xiao-shu  ZENG Hong-yan  HAN Hong  SONG Yong-li  YUAN Yun  WU Chun-yun
Institution:1. Department of Experiment Center for Medical Science Research; 2. Department of Anatomy/Histology and Embryology, Kunming Medical University, Kunming 650500;3. Kunming Medical University Haiyuan College, Kunming 651701, China
Abstract:Objective This research investigated the expression of MCP-1 in cerebral cortex of rat following middle cerebral artery occlusion (MCAO) and edaravone combination with breviscapine as a treatment of MCP-1 expression. Methods Animal models of MCAO were established, and RT-PCR,Western blot and Immunohistochemistry were used to detect the expression of MCP-1 in cerebral cortex of rats after MCAO and drug intervention. Results The expression of MCP-1 mRNA were significantly enhanced after MCAO, and became most severe at 12 h, and the difference was significant (P<0.05). The expression of MCP-1 mRNA was markedly decreased compared with the saline group after drug treatment (P<0.05); The combination of edaravone plus breviscapine was more effective than edaravone or breviscapine treatment alone (P<0.05). The expression of MCP-1 protein was significantly increased in 1d, 3d, 1 week following MCAO and stayed at a high level (P<0.05), and than obviously decreased compared with the saline group after drug treatment (P<0.05); the combination of edaravone plus breviscapine was more effective than edaravone or breviscapine alone (P<0.05) . Immunofluorescence staining showed that activated microglial cells was co-labeled with MCP-1 positive cells, and the number of MCP-1 positive cells was significantly increased after MCAO peaking at 1week. By the mean time, microglial cells did not exhibit MCP-1 positive cells in saline group. Conclusion Edaravone combination with breviscapine as a treatment could decrease the MCP-1 expression after cerebral ischemia, and the combination of edaravone plus breviscapine is more effective than edaravone or breviscapine alone.
Keywords:Cerebral ischemia  Breviscapine  Edaravone  Monocyte chemotactic protein 1  Rats  
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