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王春阳 叶冬波 倪少滨 陈起引 赵忠山 麻立.缺血后处理对大鼠肾脏miRNAs表达谱的影响[J].现代生物医学进展英文版,2015,15(28):5408-5413.
缺血后处理对大鼠肾脏miRNAs表达谱的影响
Expression Profiling of miRNAs in Rat Renal Ischemic Post-Conditioning
  
DOI:
中文关键词: 缺血后处理  肾脏  miRNAs  基因芯片
英文关键词: Ischemic Postconditioning  Renal  Mirnas  Gene Arrays
基金项目:黑龙江省教育厅科学技术研究面上项目(12521198);黑龙江省卫生厅科研课题(2012-528)
Author NameAffiliation
王春阳 叶冬波 倪少滨 陈起引 赵忠山 麻立 哈尔滨医科大学附属第一医院 
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中文摘要:
      目的:观察缺血后处理对Wistar大鼠肾组织miRNAs表达的影响。方法:将20 只Wistar 大鼠随机分为缺血再灌注组(I/R 组)和缺血后处理组(IPO 组),每组10 只。I/R 组行剖腹手术,分离双肾动脉后切除右肾,夹闭左肾动脉阻断血供,45 min 后恢复; IPoC组行剖腹手术,分离左肾动脉后将其夹闭,在阻断血液供应45 min 后恢复血供时采取10 s再灌、10 s停灌处理,反复5个周 期。在所有实验完成6 小时后,处死大鼠切除左肾,分别提取两组肾组织中的总RNA和miRNA,利用miRNA微阵列对其进行杂 交检测,通过芯片扫描和数据聚类分析,获取两组大鼠肾脏组织miRNAs 表达谱,并进行qRT-PCR 验证,筛选差异表达的 miRNAs。结果:通过qRT-PCR 验证共筛选出7 种表达差异较大的miRNAs,其中下调的三种,分别是miR-27a,miR-665, miR-let7f,上调的四种,分别为miR-532-3p,miR-205,miR-122,miR-291b。结论:差异表达miRNAs 可能参与缺血后处理减弱缺血 再灌注损伤的作用机制中。
英文摘要:
      Objective:To observe the expression profiling of miRNAs in Wistar rats renal ischemic postconditioning.Methods:According to the principle of random, the 20 Wistar rats were divided into ischemia reperfusion group (group I/R) and ischemic postconditioning group (IPO group). The I/R group underwent laparotomy, removed the right kidney after separate bilateral renal pedicle, 45 minutes after occlusion of the left renal artery to restore blood supply; the IPO group underwent laparotomy, separation of the left renal artery and then clipping it, non-invasive blood vessel occlusion 45 min after recovery of blood supply to 10 s reperfusion, 10 s stopping irrigation, 5 cycles after processing clamp. After the completion of the experiment, the kidney tissues of the I/R and IPO of the two groups of rats were removed. The total RNA and miRNA of two kidney tissues were extracted. In miRNA microarray hybridization, the chip scanning and data clustering analysis was performed, and got two groups of rat kidney miRNAs expression. Real time quantitative RT-PCR was performed to confirm the results obtained by microarray analysis.Results:By qRT-PCR validation, 7 miRNAs with great differential expression were selected, including three downregulated, respectively miR-27a, miR-665, miR-let7f, four up-regulated, respectively miR-532-3p, miR-205, miR-122, miR-291b.Conclusion:Differential expression of miRNAs may be involved in the mechanismof ischemic postconditioning which attenuated ischemia reperfusion damage.
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