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1. 成都中医药大学针灸推拿学院时间生物实验室
2. 成都中医药大学基础医学院病理教研室,成都,610075
3. 四川大学基础与法医学院生物医学工程研究室
纸质出版日期:2006
移动端阅览
唐勇, 余曙光, 陈瑾. 电针对帕金森小鼠黑质致密部脑源性神经营养因子表达的影响[J]. 针刺研究, 2006,(1):38-42.
TANG Yong~. Effect of Electroacupuncture on the Expression of BDNF and BDNF mRNA in Parkinson's Disease Mice[J]. Acupuncture research, 2006, (1): 38-42.
目的:探讨脑源性神经营养因子在电针促进帕金森小鼠黑质致密部突触可塑性中的作用。方法:24只C57BL/6J雄性小鼠
按照随机分组的原则分为空白组、空电组、模型组、电针组
每组6只。以腹腔注射(30 mg/kg)1-甲基-4苯基-1
2
3
6四氢吡啶诱导的帕金森小鼠作为研究对象
电针“合谷”“太冲”穴
频率2
1
00 Hz
电压2100 Hz
电压2
4
V
疏密波
每日1次
每次20 min
7次为1疗程
共治疗3个疗程后
分别运用免疫组化和原位杂交检测脑源性神经营养因子及其mRNA表达。结果:模型组脑源性神经营养因子免疫组化阳性细胞计数、积分光密度较空白组、空电组减少
P
<
0.05;电针组阳性细胞计数、积分光密度增加
与模型组比较P
<
0.01。模型组脑源性神经营养因子mRNA原位杂交阳性细胞计数、积分光密度较空白组和空电组减少
P
<
0.01;电针组阳性细胞计数、积分光密度增加
与模型组比较P
<
0.05。结论:电针可促进帕金森小鼠黑质致密部脑源性神经营养因子及其mRNA的表达
从而促进帕金森小鼠突触可塑性作用的发挥。
Objective: To observe the effect of electroacupuncture(EA) on the expression of brain-derived neurotrophic factor(BDNF) in substantia nigra compacta(SNC) of Parkinson's disease(PD) mice so as to study the synaptic plasticity.Methods: Twenty-four male mice(C57BL/6J) were averagely and randomly divided into normal control
EA
model and model +EA groups.PD model was induced by injection(i.p.) of 1-methyl
4-phenyl-1
2
3
6 tetrahydropyridine((30 mg/kg)).EA((2-100 Hz)
2-(4 V)
dense-sparse waves) was applied to "Hegu"(LI 4) and "Taichong"(LR 3) for(20 min)
once daily.After 21 treatments
the mice were killed for sampling SNC tissue which was then cut into sections for detecting the expression of BDNF and BDNF mRNA by immunohistochemical and in situ hybridization techniques respectively.Results: Both immunohistochemical and in situ hybridization assays showed that compared with normal control group
the number of BDNF and BDNF mRNA positive cells and integral optical density(OD) values of model group were significantly lower(P<0.05
0.01);compared with model group
the number of BDNF and BDNF mRNA positive cells and integral OD values in model +EA group were significantly higher(P<0.05
0.01).No significant differences were found among normal control
EA and model +EA groups in these indexes.Conclusion: EA can inhibit the down-regulation of expression of BDNF and BDNF mRNA of SNC in PD mice which maybe contribute to its effect in raising the synaptic plasticity of the degenerative dopaminergic neurons.
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