期刊文献+

卡马西平联合塞来昔布治疗癫痫模型大鼠的不良反应评估 被引量:1

Assessment of the adverse reactions of carbamazepine combined with celecoxib in induced epileptic rat model
下载PDF
导出
摘要 目的评估卡马西平联合塞来昔布治疗癫痫模型大鼠的不良反应。方法雄性Wistar大鼠分为假手术组、对照组及实验组,对照组及实验组以海仁酸点燃建立癫痫模型,分别给予生理盐水及卡马西平与塞来昔布联合治疗。结果治疗后3组大鼠胃窦黏膜及肾脏组织病理变化无显著差异(P>0.05);凝血功能国际标准化比值(INR)无显著差异(P>0.05);对照组及实验组心肌肌钙蛋白T(cTnT)水平显著高于假手术组(P<0.01),且实验组显著低于对照组(P<0.05)。结论卡马西平联合塞来昔布对癫痫模型大鼠的胃窦黏膜、肾脏组织、凝血功能及心肌功能均无显著不良反应,具有较高的安全性。 Objective To assess the adverse reactions of carbamazepine combined with celecoxib in treatment of induced epileptic rats.Methods Male Wistar rats were divided into sham group,control group and experimental group.Kainic acid induced epilepsy model was established and normal saline or carbamazepine combined with celecoxib were given individually to the control group and the experimental group.Results After treatment,the pathological changes of gastric antrum mucosas and kidney tissues among three groups showed no significant differences (P 〉 0.05).Coagulation international normalized ratio (INR) showed no differences among three groups (P 〉 0.05).The cardiac troponin T (cTnT) levels in the control and experimental groups were obviously higher than those in sham group (P 〈 0.01).Moreover,the cTnT level in the experimental group was lower than that in the control group (P 〈 0.05).Conclusion There were no significant adverse reactions of carbamazepine combined with celecoxib in gastric antrum mucosa,kidney tissue,coagulation and cardiac function of induced epileptic rats.
出处 《实用临床医药杂志》 CAS 2014年第23期1-4,共4页 Journal of Clinical Medicine in Practice
关键词 卡马西平 塞来昔布 癫痫 不良反应 凝血功能 心肌肌钙蛋白T Carbamazepine Celecoxib epilepsy adverse reactions coagulation cardiac troponin T
  • 相关文献

参考文献16

二级参考文献71

  • 1杨义,苏长保,吴立文,任祖渊,王任直,马文斌.发作间期PET对难治性颞叶癫痫的诊断价值[J].中华神经外科疾病研究杂志,2004,3(4):293-296. 被引量:4
  • 2蔡本志,王玲,李春莉,龚冬梅,白云龙,吕延杰,杨宝峰.氧化苦参碱对大鼠海马神经元细胞钠通道的影响[J].哈尔滨医科大学学报,2007,41(2):85-88. 被引量:6
  • 3田丽,张哲成.高同型半胱氨酸血症与神经系统疾病[J].医学综述,2007,13(10):749-751. 被引量:15
  • 4Guan QH,Pei DS,Zhang QG,et al.The neuroprotective action of SP600125,a new inhibitor of JNK,on transient brain ischemia/reperfusion-induced neuronal death in rat hippocampal CA1 via nuclear and non-nuclear pathways[J].Brain Res,2005,1035(1):51.
  • 5Liu Y,Zhang XJ,Yang CH,et al.Oxymatrine p rotects rat brains against permanent focal ischemia and downregulates NF-κB expression[J].Brain Res,2009,1268(1):174.
  • 6Pei DS,Wang XT,Liu Y,et al.Neuroprotection against ischemic brain injury by a GluR6-9c peptide containing the TAT protein transduction sequence[J].Brain,2006,129:465.
  • 7Karceski S, Morrell MJ, Carpenter D. Treatment of epilepsy in adults : expert opinion, 2005. Epilepsy Behav, 2005, 7 Suppl 1 : S1-64.
  • 8French JA, Kanner AM, Bautista J, et al. Efficacy and tolerability of the new antiepileptic drugs I. Treatment of new onset epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society. Neurology, 2004, 62: 1252-1260.
  • 9Perucca E, Gram L, Avanzini G, et al. Antiepileptic drugs as a cause of worsening seizures. Epilepsia, 1998, 39 : 5-17.
  • 10Kwan P, Brodie MJ. Early identification of refractory epilepsy. N Engl J Med, 2000, 342: 314-319.

共引文献217

同被引文献17

引证文献1

二级引证文献6

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