期刊文献+

电针对SAMP8小鼠海马Beclin-1表达的影响 被引量:8

Effects of electroacupuncture on Beclin-1 expression in hippocampus of SAMP8 mice
下载PDF
导出
摘要 目的从自噬角度探讨电针治疗阿尔茨海默症的作用机制。方法选取8月龄老年痴呆模型SAMP8小鼠16只,随机分为模型组8只和电针组8只,另选8月龄抗老年痴呆模型SAMR1小鼠8只为对照组,采用Morris水迷宫检测小鼠学习记忆能力,免疫组化法检测海马Beclin-1表达。结果与对照组比较,模型组平均逃避潜伏期明显延长,原平台象限停留时间缩短,海马Beclin-1表达降低(P<0.01);与模型组比较,电针组平均逃避潜伏期缩短,原平台象限停留时间延长,海马Beclin-1表达升高(P<0.05)。结论电针治疗阿尔茨海默症的机制可能是提高海马Beclin-1表达,增强自噬活性。 Objective To explore the therapeutic effect of electroacupuncture on Alzheimer' s disease from the point of autophagy and its mechamism.Methods Sixteen SAMP8 mice aged 8 months were randomly divided into:model group(n =8) and electroacupuncture group(n =8).Eight SAMR1 mice aged 8 months were chosen as control group.Morris water maze was used to test mice learning and memory abilities.Beclin-1 expression was determined by immunohistochemistry.Results Compared with control group,the average escape latency was significantly lengthened in model group,and the plateau phase was shortened,and Beclin-1 expression was significantly decreased(P <0.01).Compared with model group,the average escape latency significantly was shortened,the plateau phase was lengthened,and Beclin-1 expression was significantly increased in electroacupuncture group(P < 0.05).Conclusion The curative effect of electroacupuncture therapy on AD may be related to the increase of Beclin-1 expression and improvement of autophagy.
出处 《山西医科大学学报》 CAS 2015年第8期721-723,共3页 Journal of Shanxi Medical University
基金 福建省自然科学青年基金资助项目(2012J05154) 国家自然科学基金资助项目(81102625)
关键词 电针 阿尔茨海默症 海马 BECLIN-1 SAMP8小鼠 electroacpuncture Alzheimer's disease hippocampus Beclin-1 SAMP8 mice
  • 相关文献

参考文献10

  • 1H, Yu J, Jiang Z, et al. Acupuncture improves cognitive deficits and regulates the brain cell proliferation of SAMP8 mice [ J ]. Neurosei Lelt,2008,432 ( 2 ) : 111 - 116.
  • 2Wolfe DM, Lee Jtt, Kumar A,et al. Autophagy failure in Alzhei- mer' s disease and the role of defective lysosomal acidification [ J ]. Eur J Netnrosei ,2013,37 (12) : 1949 - 1961.
  • 3Manich G,Mereader C, Lynch G,et al. Characterization of amlyloid- beta granules in the hippoemnpus of SAMP8 mice[J]. J Alzheimcrs Dis ,2011,25( 11 ) :535 -546.
  • 4Pallas M ,Camins A,Snfith MA,et al. From aging to Alzheimer's dis- ease : unveiling "the switch" with the senescence-accelerated mouse model ( SAMF'8 ) [ J ]. J Alzheimers Dis ,2008,15 ( 9 ) :615 - 624.
  • 5Takeda T. Senescence-accelerated mouse(SAM) with special ref- erences to neurodegeneration models,SAMP8 and SAMP10 mice [ J ]. Neurochem Res,2009,34 ( 12 ) :639 - 659.
  • 6Cheng XR, Zhou WX, Zhang YX. The behavioral, pathological and therapeutic features of the senescence-accelerated mouse prone 8 strain as an Alzheimer' s disease animal model [ J ]. Age- ing Res Rev,2014,13( 11 ) :13 -37.
  • 7Lee S,Sato Y, Nixon RA. I,ysosomal pmteolysis inhibition selec- tively disrupts axonal transport of degradative organelles and eau- ses an Alzheimer' s-like axonal dystrophy[J]. J Neurosci ,2011, 33 (21) :7817 -7830.
  • 8Ma Q,Qiang J, Gu P, et al. Age-related autophagy alterations in the brain of senescence accelerated mouse prone 8 (SAMP8) mice [ J ]. Exp Gerontol, 2011,46 ( 7 ) :533 - 541.
  • 9Pickford F, Maslish E, Britschgi M, et al. The autophagy-rclated protein beclin 1 shows reduced expression in early Alzheimer dis- ease and tvgnlates amyloid beta accumulation in mice [ J]. J Clin Invest ,2008,118(6) :2190 -2199.
  • 10Lucin KM,O' Brien CE, Bieri G,et al. Mieroglial beclin 1 regu- lates retromer trafficking and phagocytosis and is impaired in Alzheimer~ disease [J].Neuron, 2013,79 (5) : 873 - 886.

同被引文献138

引证文献8

二级引证文献53

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部