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3-硝基丙酸多次预处理上调神经凋亡抑制蛋白表达保护多巴胺能神经元的研究
引用本文:邓学军,孙圣刚,曹学兵,李红戈,梁直厚.3-硝基丙酸多次预处理上调神经凋亡抑制蛋白表达保护多巴胺能神经元的研究[J].卒中与神经疾病,2004,11(4):203-207.
作者姓名:邓学军  孙圣刚  曹学兵  李红戈  梁直厚
作者单位:430022,武汉,华中科技大学同济医学院附属协和医院神经科
摘    要:目的研究3-硝基丙酸(3-nitropropionic acid,3-NPA)多次预处理对多巴胺能神经元的保护机制.方法应用MPTP在C57BL小鼠上制作帕金森病模型,应用爬杆、悬挂实验检测小鼠协调运动能力;应用免疫组化检测中脑黑质酪氨酸羟化酶(TH)及神经凋亡抑制蛋白(NAIP)的表达.结果在MPTP组小鼠爬杆、悬挂实验评分降低,TH表达明显减少,无NAIP表达;3-硝基丙酸单次预处理后评分增加,TH、NAIP表达增多;多次预处理后TH、NAIP表达及评分增加更明显.结论3-NPA多次预处理对多巴胺能神经元的保护机制与上调NAIP表达有关.

关 键 词:3-硝基丙酸  多次预处理  神经凋亡抑制蛋白  帕金森病
文章编号:1007-0478(2004)04-0203-05

The protective effect of 3-NPA repetitive preconditioning on dopaminergic neuron-role of upregulation of neuron apoptosis inhibitory protein
Deng Xuejun,Sun Shenggang,Cao Xuebing,et al..The protective effect of 3-NPA repetitive preconditioning on dopaminergic neuron-role of upregulation of neuron apoptosis inhibitory protein[J].Stroke and Nervous Diseases,2004,11(4):203-207.
Authors:Deng Xuejun  Sun Shenggang  Cao Xuebing  
Institution:Deng Xuejun,Sun Shenggang,Cao Xuebing,et al. Department of Neurology,Union Hospital,Tongji Medical College,HuaZhong University of Science and Technology,Wuhan 430022
Abstract:Objective To investigate the mechenism of protective effect by 3-NPA repetitive preconditioning on dopaminergic neuron. Methods MPTP was used to produce parkinson disease model. The behavioral aspect was evaluated with pole test and traction test. The positive neurons of tyrosine hydroxylase(TH) and neuron inhibitory apoptosis protein(NAIP) in the midbrain substantia nigra were asssyed by inmmuhistochemistry. Results In MPTP group, the scores of behaviour decreased significantly, and increased after single and repetitive preconditioning. The expression of TH in the midbrain substantia nigra decreased significantly (P< 0.01). After single and repetitive preconditioning, the expression of TH increased significantly (P< 0.05, P< 0.01). Otherwise, there was also significant difference between the single and repetitive preconditioning group (P< 0.05). In the control group and MPTP group, almost no NAIP expression was seen, but in the single preconditioning group, the expression of NAIP increased (P< 0.05). The number of NAIP positive cell of 3-NPA repetitive preconditioning group (P< 0.01) was much more than 3-NPA single preconditioning group (P< 0.05). Conclusion 3-NPA repetitive preconditioning had the better neuroprotective effect on the dopaminergic neuron involved in upregulating the expression of NAIP.
Keywords:3-nitropropionic acid  Repetitive preconditioning  Neuron apoptosis inhibitory protein  Parkinson disease
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