miR-183家族在噪声性聋发生发展中的表达及研究

张志远, 刘凯, 陈燕红, 等. miR-183家族在噪声性聋发生发展中的表达及研究[J]. 临床耳鼻咽喉头颈外科杂志, 2014, 28(7): 468-472. doi: 10.13201/j.issn.1001-1781.2014.07.011
引用本文: 张志远, 刘凯, 陈燕红, 等. miR-183家族在噪声性聋发生发展中的表达及研究[J]. 临床耳鼻咽喉头颈外科杂志, 2014, 28(7): 468-472. doi: 10.13201/j.issn.1001-1781.2014.07.011
ZHANG Zhiyuan, LIU Kai, CHEN Yanhong, et al. The expression of miR-183 family in the pathogenesis and development of noise-induced deafness[J]. J Clin Otorhinolaryngol Head Neck Surg, 2014, 28(7): 468-472. doi: 10.13201/j.issn.1001-1781.2014.07.011
Citation: ZHANG Zhiyuan, LIU Kai, CHEN Yanhong, et al. The expression of miR-183 family in the pathogenesis and development of noise-induced deafness[J]. J Clin Otorhinolaryngol Head Neck Surg, 2014, 28(7): 468-472. doi: 10.13201/j.issn.1001-1781.2014.07.011

miR-183家族在噪声性聋发生发展中的表达及研究

  • 基金项目:

    江西省自然科学基金项目 (No:20124BAB205001)

详细信息
    通讯作者: 张剑, E-mail:zhangjian115123@126.com
  • 中图分类号: R764.43

The expression of miR-183 family in the pathogenesis and development of noise-induced deafness

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  • 目的:建立噪声性聋动物模型,并检测不同时间段耳蜗内MicroRNA183家族成员表达量的变化,为探索噪声性聋相关的发病机制提供思路。方法:50只小鼠随机分为5个组(1、7、14、28 d实验组及对照组),每组10只。实验组给予中心频率2.0~4.0 kHz的窄带噪声,强度为100 dB SPL,每天6 h,持续3 d;对照组不接触噪声。在噪声刺激前及刺激后1、7、14和28 d后分别测得ABR阈值。通过耳蜗基膜铺片来检测毛细胞的病理损伤过程,并采用实时定量聚合酶链反应(qRT-PCR)检测MicroRNA183家族成员表达量的变化。采用SPSS 17.0 软件对数据进行统计学分析。结果:噪声刺激后,各实验组听力与刺激前及对照组相比均明显下降(均P<0.01);1 d组较其他实验组下降更明显(P<0.01),7 d组次之(P<0.05);14 d与28 d组间听力下降程度相近,差异无统计学意义(P>0.05)。铺片检测发现随着时间的延长,外毛细胞排列发生混乱、变形以及缺损数量逐渐增加,且多集中在第1和第2排,内毛细胞未见明显缺失。qRT-PCR检测显示:噪声刺激后1 d和7 d组miR-183/96/182的表达量均较对照组下降(均P<0.01),而1 d与7 d组间差异无统计学意义(P>0.05);14 d组的表达量呈明显上升趋势(P<0.01);28 d组表达量较14 d组明显回降(P<0.01),但仍高于1 d组和7 d组(P<0.01)。结论:MicroRNA183家族成员在噪声刺激后的一段时间内表达量存在着显著变化,可能作为特异性基因在噪声性聋发生发展中起着重要作用。
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出版历程
收稿日期:  2013-02-02

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