›› 2009, Vol. 40 ›› Issue (4): 555-559.doi: 10.3969/j.issn.0529-1356.2009.04.008

• 论著 • 上一篇    下一篇

尼古丁对PD大鼠黑质多巴胺能神经元变性的影响

李春丽;王志刚;翟秀岩*   

  1. 中国医科大学基础医学院发育生物学教研室,沈阳 11000
  • 收稿日期:2008-04-22 修回日期:2008-09-16 出版日期:2009-08-06
  • 通讯作者: 翟秀岩

Effect of nicotine on the degeneration of dopaminergic neurons in the substantia nigra of PD rats

  1. Department of Developmental Biology, College of Basic Medical Sciences, China Medical University, Shenyang 110001, China
  • Received:2008-04-22 Revised:2008-09-16 Online:2009-08-06
  • Contact: ZHAI Xiu-yan

关键词: 尼古丁, 帕金森病, 脂多糖, 小胶质细胞, 多巴胺, 免疫印迹法, 反转录-聚合酶链式反应, PD大鼠

Abstract: Objective To explore the effect of nicotine on the degeneration of dopaminergic neurons in PD rats. Methods Forty-five SD rats were randomly divided into three groups: PBS group (CON), normal saline + LPS ( NS ) group and nicotine +LPS ( NIC ) group. On 24 hours after LPS or PBS injection, inducible nitric oxide synthase ( iNOS ) protein expression was examined by immunoblotting. ON 14d after LPS or PBS injection, the numbers of tyrosine hydroxylase ( TH ) positive neurons and morphological changes of OX-42 positive cells in the substantia nigra(SN) were observed by immunohistochemistry. TH mRNA and TH protein expressions were examined by RT-PCR or immunoblotting. Results Compared with CON group, iNOS protein increased markedly 24 hours after LPS injection in NS group. TH positive neurons, TH mRNA and TH protein in the SN decreased remarkably 14 days after nigrainjiection. Most of microlglial showed big cell body with thicker and shorter processes. However, nicotine reversed the above changes, Compared with NS group, TH positive neurons, TH mRNA and TH protein in the SN increased remarkably in NIC. Besides, most microglia showed small cell body with slim and long processes. Conclusion Nicotine could prevent LPSinduced degeneration of DA neurons, probably because of that the pretreatment with nicotine blocks the activation of microglia and the expression iNOS protein.

Key words: Nicotine, Parkinson’s disease, Lipopolysaccharide, Microglia, Dopamine, Western blotting, RT-PCR, PD Rat

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