期刊文献+

苯妥英钠耐药鼠神经元保护基因的表达 被引量:3

Neuron protection genes expression in PHT resistant epileptic rats with cDNA microarray
下载PDF
导出
摘要 目的 :探索神经元自身保护基因在苯妥英钠耐药鼠和非耐药鼠中的差异表达。方法 :选择成年Wistar大鼠用电刺激杏仁核方法建立耐PHT和非耐药癫大鼠模型 ,应用含有 4 0 96条人类全长基因的cDNA表达谱芯片 ,检测耐药与非耐药组神经元保护基因表达谱的差异。结果 :发现 10条神经元自身保护基因的表达在两组间存在差异。结论 :神经元自我保护机制的降低可能是难治性癫形成的原因之一。 Objective:To determine the differential neuron protection genes expression in drug resistant and drug responder epileptic rat model.Methods:Adult Wistar rats were seleted to prepare PHT resistant and PHT responder epilepsy model. The cDNA microarray containing four thousand and ninety six human target genes was used to determine the difference of neuron protection gene expression spectrum between drug resistant group and drug responder group.Results:Difference between PHT resistant and PHT responder epileptic rats was noted in 10 neuron protection genes.Conclusion:The decrease of neuron protection mechanism might be one of the causes of intractable epilepsy.
出处 《临床神经电生理学杂志》 2004年第1期31-34,共4页 Journal of Clinical Electroneurophysiology
基金 卫生部科学研究基金资助 (98-1-3 5 4) 重庆市卫生局科研基金资助(0 1-2 -0 3 1)
关键词 苯妥英钠 耐药 大鼠 神经元保护基因 cDNA表达谱 癫痫 基因芯片技术 cDNA microarray intractable epilepsy phenytoin animal model
  • 相关文献

参考文献13

  • 1肖争,晏勇,王学峰.大鼠耐苯妥英钠和苯巴比妥钠杏仁核点燃模型及多药耐受基因的表达[J].中华神经科杂志,1999,32(6):365-368. 被引量:26
  • 2曾可斌,王学峰,文世全,沈鼎烈,晏勇.cDNA芯片检测耐/非耐苯妥英钠癫痫鼠脑线粒体基因的差异表达[J].中华神经外科杂志,2002,18(4):234-237. 被引量:7
  • 3王学峰 见:王学峰 肖波 孙红斌主编.难治性癫痢的发病机制[A].见:王学峰,肖波,孙红斌主编.难治性癫痫[C].上海科技出版社,2002.25.
  • 4Albright PS, Burnham WM. Development of a new pharmacological seizure model:effects of anticonvulsanta on cortical and amygdala kindled seizure in rat[J]. Epilepsia, 1980,21:681-689.
  • 5Rundfeldt C, Honack D, Loscher W. Phenytoin potently increases the threshold for focal seizure in amygdala kindled rats[J]. Neuropharmacology, 1990,29 :845-851.
  • 6SharpFR, Massa SM, Swanson R A, et al. Heat-shock protein protection Trends[J]. Neurosci,1999,22:97-99.
  • 7Yenari MA, Fink SL, Sun GH, et al, Gene therapy with HSP72 is neuroprotective in rat models of stroke and epilepsy[J]. Ann Neurol,1998,44:584-91.
  • 8Head MW, Corbin E, Goldman JE, et al. Overexpression and abnormal modification of the stress proteins alpha B-crystallin and HSP27 in alexander disease[J]. Am J pathol, 1993, 143:1743-1753.
  • 9Tanaka H,Grooms SY, Bennett MV, et al. The AMPAR subunit GIuR2: still front and center-stage[J]. Brain Res,2000,886:190-207.
  • 10Oner P, Kocak H,Oztas B, et al. Effects of streptozotocin induced diabetes and pentylenetetrazol induced seizure on brain cortex (Ca2+)ATPase activity in rats[J]. Int J Neurosci, 2000,103:33-40.

二级参考文献9

共引文献31

同被引文献27

  • 1刘崇铭 高殿振 周新华 等.东亚钳蝎毒及其成分抗癫痫肽的抗惊厥作用[J].沈阳药学院学报,1988,5(2):110-111.
  • 2Lazarowski A, Massaro M, Schteinschnaider A, et al. Neuronal MDR-1 gene expression and persistent low levels of anticonvulsant in a child with refractory epilepsy [ J ]. Ther Drug Monit, 2004, 26( 1 ) :44.
  • 3Voskuyl B A, Dingemanse J, Danhof M. Determination of the threshold for convulsions by direct cortical stimulation[J]. Epilepsy Bes, 1989,3 : 120.
  • 4Loscher W, Rundfeldt C. Kindling as a model of drug-resistans partial epilepsy: Selection of phenytoin-resistant and monresistant rats[J]. J Pharmacol Exp Ther, 1991,258:483.
  • 5Tishler D M, Weinbeig K I, Hinton D R. MDR1 gene expression in brain of patients with medically intractable epilepsy [ J ]. Epilepsia, 1995,36:1.
  • 6Schmidt D, Loscher W. Drug resistance in epilepsy: Putative neurobiologic and clinical mechanism [J]. Epilepsia, 2005,46 (6) :858.
  • 7Jiang M,Ma Y,Cheng H,et al.Molecularcloning and characterization of a novel human gene (HSPBAP1) from human fetalbrain.Cytogenet Cell Genet,2001,95:48-51.
  • 8Akbar MT,Lundberg AM,Liu K,et al.The neuroprotective effects of heat shock protein 27overexpression in transgenic animals against kainate-induced seizures and hippocampal celldeath.J Biol Chem,2003,278:19956-19965.
  • 9Charette SJ,Lavoie JN,Lambert H,et al.Inhibition of Daxxmediated apoptosis by heatshock protein 27.Mol Cell Biol,2000,20:7602-7612.
  • 10Brar BK,Stephanou A,Wagstaff M J,et al.Heat shock proteins delivered with a virusvector can protect cardiac cells against apoptosis as well as against thermal or hypoxicstress.J Mol Cell Cardiol,1999,31:135-146.

引证文献3

二级引证文献7

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