浏览全部资源
扫码关注微信
1. 北京中医药大学针灸推拿学院
2. 北京中医药大学基础医学院
3. 北京中医药大学科研中心
纸质出版日期:2014
移动端阅览
薛卫国, 张忠, 许红, 等. 电针对APP转基因鼠神经元自噬途径的影响[J]. 针刺研究, 2014,39(4):272-277.
XUE Wei-guo, ZHANG Zhong, XU Hong, et al. Effect of Electroacupuncture Intervention on Autophagy Pathway in APP 695V717I Transgenic Mice[J]. Acupuncture research, 2014, 39(4): 272-277.
薛卫国, 张忠, 许红, 等. 电针对APP转基因鼠神经元自噬途径的影响[J]. 针刺研究, 2014,39(4):272-277. DOI: 10.13702/j.1000-0607.2014.04.003.
XUE Wei-guo, ZHANG Zhong, XU Hong, et al. Effect of Electroacupuncture Intervention on Autophagy Pathway in APP 695V717I Transgenic Mice[J]. Acupuncture research, 2014, 39(4): 272-277. DOI: 10.13702/j.1000-0607.2014.04.003.
目的:从神经元自噬途径的角度
探讨电针治疗阿尔茨海默病的可能作用机制。方法:将12只13月龄APP转基因雌性小鼠随机分为模型组和电针组
以相同月龄和背景的C 57BL/6小鼠6只做对照组。电针组取"百会""涌泉"穴
疏密波
频率2Hz/100Hz
强度1
2
mA
每次留针15min
隔日1次
治疗3个月。每组6只动物取半脑做纹状皮层常规Aβ1-42免疫组化、TUNEL染色
取另半脑做纹状皮层透射电镜观察。结果:免疫组化结果显示
Aβ1-42主要表达于皮层锥体神经元
与对照组相比
模型组Aβ1-42细胞内表达增强(P
<
0.01);透射电镜结果显示
模型组皮层神经元胞体及突起有大量自噬体;TUNEL染色显示
与对照组相比
模型组皮层凋亡细胞数目增多(P
<
0.01)。而电针组Aβ1-42细胞内表达减弱(P
<
0.01)
神经细胞自噬体明显减少
凋亡细胞数目减少(P
<
0.05)。结论:APP 695V717I转基因鼠存在神经元自噬途径功能紊乱及神经元内Aβ1-42水平增高;对神经元自噬途径功能的调节
可能是电针改善阿尔茨海默病的作用机制之一。
Objective To observe the effect of electroacupuncture(EA)therapy on the intraneuronal Aβ1-42 and dysfunction of autophagy pathway
so as to reveal its mechanism underlying improvement of Alzheimer's disease(AD).MethodsAPP 695V717 Itransgenic female mice were randomly divided into model group(n=6)and EA group(n=6);and C 57BL/6mice were used as the control group(n=6).After 3months' treatment by EA therapy at"Baihui"(GV 20)and"Yongquan"(KI 1)(15min
once every other day
2Hz/100 Hz
1-2mA)
the expression level of Aβ1-42 of the striate cortex was detected by immunohistochemistry.TUNEL staining was used to detect the degree of apoptosis of the striate cortex
and ultrastructural changes of autophagosome in the cortex were observed using electron microscope.Results In comparison with the control group
Aβ1-42 expression level and the apoptotic neurons in the striate cortex were significantly up-regulated in the model group(P<0.01).Following EA intervention for 3months
the Aβ1-42 expression level and the number of apoptotic neurons were significantly decreased in the EA group(P<0.01
P<0.05).Accordingly
transgenic induced dark degenerated neurons exhibiting irregular body deformation
analosis
and abundant secondary lysosomes and autophagosomes were reduced in the EA group.Conclusion EA intervention can effectively down-regulate Aβ1-42 expression and number of the apoptotic neurons in the striate cortex in APP transgenic model mice
which may contribute to its effect in improving pathological changes of ultrastructure of neurons.
0
浏览量
439
下载量
30
CNKI被引量
关联资源
相关文章
相关作者
相关机构