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作 者:黄飞[1] 李亚男[2] 尹飞[1] 赵东旭[1] 武云涛[1] 李野[1] 刘景臣[1] 朱庆三[1]
机构地区:[1]吉林大学第一医院脊柱外科,长春130021 [2]吉林大学第一医院儿科,长春130021
出 处:《中国免疫学杂志》2013年第5期495-498,共4页Chinese Journal of Immunology
摘 要:目的:在整体水平研究脊髓缺血再灌注损伤对大鼠水通道蛋白4表达水平的影响。方法:SD大鼠72只随机分为空白组、假手术组和SCII组,每组24只。建立大鼠脊髓缺血再灌注损伤模型,并于1、3、5、7天四个时间点分别处死6只。BBB评分评价神经功能,Western blot和免疫荧光方法检测AQP4的表达情况。结果:空白对照组和假手术组在不同时间点的BBB评分均为21分,SCII组的BBB评分在1天时最低,随时间推移逐渐增加,3天明显优于1天(P<0.05),5天明显优于3天(P<0.05),5天明显优于7天(P<0.05)。Western blot在34 kD及43 kD分子量处可见特异性条带,SCII组早期AQP4的表达水平显著下降,即在1、3、5、7天四个时间点AQP4的表达显著低于空白对照组和假手术组,但呈逐渐增加趋势;在7天仍显著低于正常空白组和假手术组(P<0.05)。免疫荧光检测AQP4的表达变化趋势与Western blot的检测结果相似。结论:SCII存在AQP4低表达,这可能是造成SCII神经功能障碍的重要原因。Objective: To explore the effect of spinal cord ischemia-reperfusion injury(SCII) on aquqporin4(AQP4) in a SCII rat model.Methods: Seventy-two Sprague-Dawley(SD) rats were randomly divided into three groups with twenty-four rats in each group.The groups were: blank group;sham operation;and SCII group at 1,3,5,or 7 days after reperfusion started,six rats of every group were then killed.BBB scoring system to evaluate the nerve function,and the expression of AQP4 was determined by Western blot and immunofluorescence.Results:At different time,the BBB score of blank group and sham operation have no fluctuations,and has no significant differences.In SCII group,the BBB score has a dynamic change,with a significant increasing at 1~7 d,3 days significantly better than 1 day(P0.05),5 days significantly better than 3 days(P0.05),5 days significantly better than 7 days(P0.05).Western blot specific bands of AQP4 visible at a molecular weight of 34 kD and 43 kD,the AQP4 protein production of SCII was markedly lower than those of blank group at 1,3,5 and 7 d,respectively.The AQP4 level increased gradually,but still lower than that of blank group and sham operation group in 7 days(P 0.05).At the same time,the AQP4 measured also by immunofluorescence,the expression of AQP4 is similar to the AQP4 level measured by Western blot(P0.05).Conclusion:The AQP4 level was significantly decreased in the SCII,indicating that the low expression of AQP4 might play an important role in the mechanisms of SCII neurological dysfunction.
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