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山东大学学报(医学版) ›› 2010, Vol. 48 ›› Issue (11): 50-53.

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锂-匹罗卡品致痫大鼠海马结构nNOS、iNOS及活化Caspase-3蛋白表达的动态变化

陈立光1,刘滨2,范海涛2,贾践博2,庞琦2   

  1. 1. 山东省医学影像学研究所,济南 250021;2. 山东大学附属省立医院神经外科, 济南 250021
  • 收稿日期:2010-08-17 出版日期:2010-11-16 发布日期:2010-11-16
  • 通讯作者: 庞琦(1961- ),男,教授,博士研究生导师,主要从事神经系统肿瘤、脑血管疾病及功能神经外科疾病的临床及病理学研究。 E-mail: pangqi@sdu.edu.cn
  • 作者简介:陈立光(1965- ),男,副主任医师,主要从事磁共振、CT对神经系统及消化系统疾病的诊断研究。
  • 基金资助:

    山东省卫生厅医药卫生发展计划项目(2009HZ053)

Dynamic changes of nNOS, iNOS and activated Caspase-3 protein  expressions  in the hippocampus of rats with lithium-pilocarpine-induced epilepsy

CHEN Li-guang1, LIU Bin2, FAN Hai-tao2, JIA Jian-bo2, PANG Qi2   

  1. 1. Shandong Medical Imaging Research Institute, Shandong University, Jinan 250021, China;
    2. Department of Neurosurgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China
  • Received:2010-08-17 Online:2010-11-16 Published:2010-11-16

摘要:

目的    探讨大鼠癫痫持续状态(SE)后海马结构神经型一氧化氮合酶(nNOS)、诱导型一氧化氮合酶(iNOS)及活化Caspase-3蛋白表达的动态变化及其相互关系。 方法    采用锂-匹罗卡品腹腔注射建立大鼠SE模型,用免疫组织化学及免疫印迹法在2h、6h、3d及7d不同时相点检测大鼠海马nNOS、iNOS 及活化Caspase-3蛋白的表达。 结果     大鼠海马nNOS的蛋白表达在SE后2h开始迅速增高,在6h时达到高峰,之后逐渐降低,但在3、7d时仍显著高于对照组(P均<0.01)。iNOS蛋白的表达在SE后6h时开始持续增高(P<0.01),并在7d时达到高峰(P<0.01)。活化Caspase-3蛋白的表达在3d开始增高(P<0.01),7d时达到高峰(P<0.01)。 结论    大鼠在SE后海马的nNOS、iNOS及活化Caspase-3的表达均有不同程度的增高,提示一氧化氮合酶的反应产物一氧化氮可能与癫痫发作后海马结构内的神经元受损有关,而神经元受损与凋亡之间的关系亦密不可分。

关键词: 癫痫持续状态;模型,动物;海马;Caspase蛋白;一氧化氮合酶;细胞凋亡;大鼠,Wistar

Abstract:

Objective    To explore the correlation and dynamic changes of protein expressions of nNOS, iNOS and activated Caspase-3 after status epilepticus (SE). Methods       The animal model was established by lithium-pilocarine induction in rats. 2h, 6h, 3d and 7d after SE, variations of expressions of nNOS, iNOS and activated Caspase-3 proteins were determined by immunohistochemistry and immunoblot, respectively. Results    Expression of the nNOS protein significantly increased 2h  after SE(P<0.01), reached its peak at 6h (P<0.01), and decreased thereafter. However, expressions of the nNOS protein on 3d and 7d were still significantly higher compared with the control group (P<0.01). Expression of the iNOS protein was significantly up-regulated 6h after SE(P<0.01), and reached its peak on 3d (P<0.01). Expression of the activated Caspase-3 protein significantly increased 3d  after SE(P<0.01), and reached its peak on 7d (P<0.01). Conclusion     Expressions of nNOS, iNOS and activated Caspase-3 proteins are up-regulated at different levels in the rat hippocampus at different times after SE, suggesting that the activation of Caspase-3 may be involved in the excitotoxic effect induced by nitric oxide synthase (NOS)  and apoptosis could be closely related to neuron injury.

Key words: Status epilepticus; Models, animal; Hippocampus; Caspase protein; Nitric oxide synthase; Apoptosis; Rat, Wistar

中图分类号: 

  • R651.1
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