文章摘要
王凤军,李红颖,李 宏,孙悦微,姜杨薇,陈元元,宋婷婷.脑源性神经生长因子对齿状回miR-132表达及抑制性电流的影响[J].,2017,17(4):633-635
脑源性神经生长因子对齿状回miR-132表达及抑制性电流的影响
Effect of BDNF on The Levels of miRNA-132 and sIPSCs in the Dentate Gyrus of MTLE
投稿时间:2016-09-30  修订日期:2016-11-02
DOI:10.13241/j.cnki.pmb.2017.04.008
中文关键词: 脑源性神经生长因子  颞叶内侧癫痫  miRNA-132  自发性抑制性突触后电流
英文关键词: BDNF  MTLE  miRNA-132  sIpscs
基金项目:黑龙江省卫生厅科研基金项目(2013101)
作者单位E-mail
王凤军 哈尔滨医科大学附属第四医院 神经内科 黑龙江 哈尔滨 150001 fengjun19791209@163.com 
李红颖 哈尔滨市第二医院 神经康复科 黑龙江 哈尔滨 150056  
李 宏 哈尔滨医科大学附属第四医院 神经内科 黑龙江 哈尔滨 150001  
孙悦微 哈尔滨医科大学附属第四医院 神经内科 黑龙江 哈尔滨 150001  
姜杨薇 哈尔滨医科大学附属第四医院 神经内科 黑龙江 哈尔滨 150001  
陈元元 哈尔滨医科大学附属第四医院 神经内科 黑龙江 哈尔滨 150001  
宋婷婷 哈尔滨医科大学附属第四医院 神经内科 黑龙江 哈尔滨 150001  
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中文摘要:
      摘要 目的:探讨脑源性神经生长因子(BDNF)对海马miR-132的表达及齿状回颗粒细胞抑制性突触后电流(sIPSCs)的影响,明确BDNF对颞叶内侧癫痫(MTLE)发病机制的作用。方法:选取哈医大一院神经外科2008年4月-2010年10月手术治疗的MTLE患者12例海马组织。RT-pcr技术检测BDNF孵育后mir-132表达,脑片膜片钳技术检测BDNF对sIPSCs的影响。结果:BDNF升高了颞叶癫痫海马miRNA-132的表达(P<0.01),减弱了颗粒细胞sIPSCs的频率和幅度(P<0.01)。结论:BDNF升高了海马mir-132的表达,减弱颗粒细胞sIPSCs的频率和幅度,可能对MTLE的发展有促进作用。
英文摘要:
      ABSTRACT Objective: To study the effect of brain derived neurotrophic factor (BDNF) on the levels of miRNA-132 and sIPSCs in the dentate gyrus of patients with MTLE. Methods: The study was performed from April 2008 to October 2010. Surgically removed specimens were collected from the patients with MTLE. All patients gave written informed consent for research use of the biopsy materials. Surgically resected hippocampal were collected and immediately immersed in oxygenated ice-cold SACSF. The expression of mIR-132 by RT-PCR and sIPSCs by patch-clamp. Results: The expression of miR-132 was significantly increased in Dentate Gyrus of MTLE patients after BDNF perfusion was significantly higher than that before perfusion P<0.01). The frequency and amplitude of sIPSC were obviously lower in Dentate Gyrus of MTLE patients after BDNF perfusion was significantly higher than that before perfusion (P<0.01). Conclusion: BDNF increased the expression of miR-132 and inhibited the frequency and amplitude of sIPSCs of granule cells in the hippocampus of MTLE patients after operation, which could contribute to the development of MTLE.
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