期刊文献+

癫癎发作过程中细胞凋亡与一氧化氮合酶、核因子-B的关系 被引量:1

Relationship of nitric oxide synthase,NF-κB and cell apoptosis in epilepsy
下载PDF
导出
摘要 目的探讨癫癎发作过程中细胞凋亡与一氧化氮合酶(NOS)、核因子-B(NF-B)的关系。方法采用戊四氮(PTZ)致癎大鼠模型,检测癫癎发作后神经细胞凋亡、NOS和NF-B的变化。结果细胞凋亡率在癫癎发作后6 h开始升高,至24 h达到高峰,48 h下降,与对照组比较差异有显著性(P<0.05)。NOS在癫癎发作后1 h、24 h有2个分泌高峰,与对照组比较差异有显著性(P<0.05);对照组大鼠海马没有NF-B核转位细胞,而致癎后NF-B核转位细胞显著上调,24 h达高峰(P<0.01)。结论PTZ致癎大鼠模型中NOS早期可能参与癫癎发生,后期可能通过诱导NF-B产生而参与了神经细胞的凋亡。 Objective To investigate the relationship of nitric oxide synthase ( NOS), nuclear factor - KB ( NF - KB) and cell apoptosis in epilepsy. Methods Animal model of epilepsy was established by pentylenetetrazol (PTZ) induction in rats. Following epilepsy seizure, the variations of apoptosis levels of the nerve cells at the different times, NOS and the activity of NF - KB in the rat hippocampus were determined by flow cytometry ( FCM ) , chromatometry and immunohistochemistry, respectively. Results The apoptosis rate increased 6 h after seizure, reached its peak at 24 h and decreased at 48 h. The statistical differences were considered significant compared with the control group ( P 〈 0.05 ). The levels of NOS had two respective secretion peaks 1 b and the 24 h after epilepsy, and had the significant differences compared with the control group ( P 〈 0.05 ). In the control group, there were no cells with nuclear translocation of NF - KB in the rat hippocampus, while the expression of cells with nuclear translocation of NF - KB in the PTZ group was remarkably upregulated and reached its peak 24 h after seizure ( P 〈 0.01 ). Conclusion In the PTZ group, NOS may participate in the seizure generation in the early stage, while in the latter stage it may be involved in cell apoptosis by inducing the activation of NF - KB.
出处 《徐州医学院学报》 CAS 2009年第2期111-113,共3页 Acta Academiae Medicinae Xuzhou
基金 徐州市科技计划项目(2006-35)
关键词 癫癎 细胞凋亡 一氧化氮合酶 NF-B epileosy cell apoptosis nitric oxide synthase NF - KB
  • 相关文献

参考文献6

二级参考文献23

共引文献17

同被引文献21

  • 1颜峰平,陈忆九,黄晓华.大鼠皮肤挫伤后Beclin1和LC3的表达[J].法医学杂志,2007,23(1):11-13. 被引量:5
  • 2Sankar R, Rho JM. Do seizures affect the developing brain? Lessons from the laboratory [ J ]. Child Neurol,2007,22 (5 suppl) :21 -29. 被引量:1
  • 3Silverstein FS, Jensen FE. Neonatal seizures[ J]. Ann Neurol, 2007,62 (2) :112-120. 被引量:1
  • 4Chiricozzi F, Chieffo D, Battaglia D, et al. Developmental plasticity after righthemispherectomy in an epileptic adolescent with early brain injury [ J]. Childs Nerv Syst ,2005,21 (11 ) :960 -969. 被引量:1
  • 5Rubinsztein DC. The roles of intracellular protein - degradation pathways in neurodegeneration[J].Nature,2006,443(7113) :780-786. 被引量:1
  • 6Rubinsztein DC, di Fiqla M, Heintz N, et al. Autophagy and its possible roles in nervous system diseases, damage and repair [J]. Autophagy, 2005,1(1) :11 -22. 被引量:1
  • 7Jiang Q, Wang JM, Wu XR, et al. Alterations of NR2B and PSD - 95 expression after early - life epileptiform discharges in developing neurons[J]. Int J Devl Neurosei ,2007,25 ( 3 ) : 165 - 170. 被引量:1
  • 8Rami A, Langhagen A ,Teiger S. Focal cerebral ischemia induces upregulation of Beclinl and autophagy -like cell death[J].Neurobiol Dis, 2008,29( 1 ) : 132 - 141. 被引量:1
  • 9Yoshimori T. Autophagy:A regulated bulk degradation process inside cells [ J ]. Biochem Biophys Res Commun,2004, 313 ( 2 ) : 453 - 458. 被引量:1
  • 10Reggiori F, Klionsky DJ. Autophagosomes : Biogenesis from scratch [J]. ? Curr Opin Cell Biol,2005 ,17 ( 4 ) :415 -422. 被引量:1

引证文献1

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部