期刊文献+

全蝎醇提物与丙戊酸干预氯化锂-匹罗卡品慢性点燃模型大鼠癫痫发作的疗效比较 被引量:9

Effects of Ethanol Extracts of Scorpion and Valproic Acid in the epileptic rat model induced by Lithium Chloride-Pilocarpine:A comparative study
下载PDF
导出
摘要 目的探讨全蝎醇提物(Ethanol Extracts of Scorpion,EES)与丙戊酸(Valproic Acid,VPA)干预氯化锂-匹罗卡品(Lithium Chloride-Pilocarpine,Licl-Pilo)慢性点燃模型大鼠癫痫发作的疗效。方法 186只成年雄性大鼠除6只设为正常对照组外,其余均建立Licl-Pilo慢性点燃大鼠模型,造模成功后分为模型组、VPA干预组、低EES剂量干预组(EESL干预组)、中EES剂量干预组(EESM干预组)和高EES剂量干预组(EESH干预组)各36只。正常对照组、模型组分别灌胃给予等容积的生理盐水,VPA干预组灌胃给予VPA溶液[浓度为120 mg/(kg.d)],EESL干预组、EESM干预组、EESH干预组灌胃给予EES溶液[浓度分别为290 mg/(kg.d)、580 mg/(kg.d)及1160 mg/(kg.d)],观察30天内致痫大鼠慢性癫痫自发性发作(spontaneous seizures,SRS)、发作级别、发作次数,并进行组间比较。结果 Licl-Pilo慢性点燃模型鼠的造模成功率为85.65%,各实验组SRS发生频率5~15次/周。治疗后,EESM干预组、EESH干预组和VPA干预组癫痫大鼠痫性发作级别及SRS发作次数与模型组比较差异有统计学意义(P<0.05);EESL干预组治疗效果不明显,与模型组比较差异无统计学意义(P>0.05)。结论一定剂量的EES能显著降低癫痫大鼠的自发性发作,且与疗效呈明显的量效关系,即剂量越大疗效越好,该结果为EES的抗癫痫作用提供了行为学依据。 A comparative study on the antiepileptic effects of Ethanol Extracts of Scorpion(EES) and Valproic Acid(VPA) in epileptic rat model induced by Lithium Chloride-Pilocarpine(Licl-Pilo). Of 186 adult male SD rats,6 served as normal controls(control group),the others were injected with Licl-Pilo as the epileptic rat model.The model rats were randomly assigned to the Licl-Pilo group(n=36),the VPA group(n=36),the low-dose EES group(EESL,n=36),the middle-dose EES group(EESM,n=36),and the high-dose EES group(EESH,n=36).Rats in control and Licl-Pilo group were intragastrically administrated with isometric Sodium Chloride.The other model rats were intragastrically administrated with VPA 120 mg/(kg·d),EES 290 mg/(kg·d),EES 580 mg/(kg·d),and EES 1160 mg/(kg·d) respectively.The model rats were observed for 30 days on the severity and frequency of chronic spontaneous seizures(SRS) which were also compared among groups. The success rate of the epileptic rat model was 85.65%.The mean incidence of SRS in all model rats ranged from 5 to 15 times per week.After treatment,the severity and frequency of SRS were significantly different between the Licl-Pilo,EESM,EESH and VPA group(P 0.05).No significant difference was observed between the EESL and Licl-Pilo group(P 0.05). EES can significantly reduce the incidence of SRS.There is an obvious dose-effect relation between EES and SRS.Those results provide behavioral evidences for the antiepileptic effect of EES.
出处 《实用医院临床杂志》 2012年第2期52-54,共3页 Practical Journal of Clinical Medicine
关键词 全蝎醇提物 丙戊酸 氯化锂-匹罗卡品 癫痫 大鼠 Ethanol Extracts of Scorpion Valproic Acid Lithium Chloride-Pilocarpine Epilepsy Rat
  • 相关文献

参考文献12

  • 1李万忠,姚金成,何群.全蝎、蜈蚣醇提工艺的研究[J].潍坊医学院学报,2006,28(5):345-346. 被引量:9
  • 2Guo J,Liu J,Fu W,et al.The effect of electroacupuncture on spontaneous recurrent seizure and expression of CAD67 mRNA in dentate gyms in a rat model of epilepsy[J].Brain Res,2008,1188(1) ;165-172.
  • 3Racine RJ.Modification of seizure activity by electrical stimulation.II.Motor seizure[J].Electr oencephalogr Clin Neurophysiol,1972,32(3):281-294.
  • 4Sharma AK,Reams RY,Jordan WH,et al.Mesial temporal lobe epilepsy:pathogenesis,induced rodent models and lesions[J].Toxicol Pathol,2007,35(7):984-999.
  • 5Tanriverdi T,Poulin N,Olivier A.Psychosocial Outcome after Extra-temporal Epilepsy Surgery; A Prospective Clinical Study[J].Turk Neurosurg,2008,18(2):114-124.
  • 6Pellock JM.Overview:Definitions and Classification of Seizure Emergencies[J].J Child Neurol,2007,22(1):9-13.
  • 7Rogawski MA.Loscher W.The neurobiology of antiepileptic drugs[J].Nat Rev Neurosci,2004,5(4):553-564.
  • 8Kaindl AM,Asimiadou S,Manthey D,et al.Antiepileptic drugs and the developing brain[J].Cell Mol Life Sci,2006,63(3):399413.
  • 9Zhao R,Zhang XY,Yang J,et al.Anticonvulsant effect of BmK IT2,a sodium channel-specific neurotoxin,in rat models of epilepsy[J].BrJ Pharmacol,2008,154(11):1116-1124.
  • 10Fattorusso R,Frutos S,Sun X,et al.Traditional Chinese medicines with caspase-inhibitory activity[J].Phytomedicine,2006,13(1):16-22.

二级参考文献11

  • 1李万忠,姚金成,何群.全蝎、蜈蚣醇提工艺的研究[J].潍坊医学院学报,2006,28(5):345-346. 被引量:9
  • 2张映琦,廖维宏,迟路湘,陈康宁,史树贵,范文辉,陈贞芳.匹罗卡品致大鼠癫痫持续状态后海马神经元凋亡的动态观察[J].第三军医大学学报,2007,29(1):71-73. 被引量:12
  • 3Pellock JM. Overview: Definitions and Classifications of Seizure Emergencies[J]. J Child Neurol, 2007, 22:9-13.
  • 4Liou AK, Clark RS, Henshall DC, et al. To die or not to die for neurons in ischemia, traumatic brain injury and epilepsy: a review on the stress- activated signaling pathways and apoptotic pathways [J]. Prog Neurobiol, 2003,69:103-142.
  • 5Nicholson DW, Thomberry NA.Caspases killer proteases[J] Trends in Biochemical Science,1997,22:299-306.
  • 6Narkilahti S, Nissinen J, Pitkanen A. Administration of caspase-3 inhibitor during and after status epilepticus in rats effect on neuronal damage and epileptogenesis[J]. Neuropharmacology,2003, 44:1068-1088.
  • 7Puig B, Ferrer I. caspase-3-associated apoptotic cell death in excitotoxic necrosis of the entorhinal cortex following intraperitoneal injection of kainic acid in the rats[J]. Neurosci Lett, 2002, 321:182-186.
  • 8Jung KH, Chu K, Kim M, et al. Continuous cytosine-b-D- arabinofuranoside infusion reduces ectopic granule cells in adult rat hippocampus with attenuation of spontaneous recurrent seizures following pilocarpine- induced status epilepticus[J]. Eur. J. Neurosci, 2004, 19:3219-3226.
  • 9Racine RJ.Modification of seizure activity by electrical stimulation. ll.Motor seizure[J]. Electroencephalogr Clin Neurophysiol,1972, 32:281-294.
  • 10Henshall DC, Simon RP. Epilepsy and apoptosis pathways[J]. Cereb. Blood Flow Metab,2005,25:1557-1572.

共引文献32

同被引文献165

引证文献9

二级引证文献58

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