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不同药物诱导的小鼠癫痫模型的差异性研究
引用本文:胡琳,张华丹,陈亚天,华男,曾玲晖.不同药物诱导的小鼠癫痫模型的差异性研究[J].浙江大学学报(医学版),2013,42(6):609-614.
作者姓名:胡琳  张华丹  陈亚天  华男  曾玲晖
作者单位:浙江大学城市学院医学院,浙江 杭州 310015
基金项目:教育部留学回国科研启动基金资助项目;杭州市科技发展计划基金资助项目(20100333T24).
摘    要:目的:比较ICR小鼠对常用致痫药物匹罗卡品、红藻氨酸以及戊四氮的差异性反应,为ICR品系小鼠用作常规癫痫研究奠定基础。 方法:成年雄性ICR小鼠给予不同的药物(匹罗卡品、红藻氨酸、戊四氮)诱发急性痫性发作,在癫痫持续状态发作(SE)2h后终止,分别于造模后7 d采用Fluro-Jade B染色观察兴奋性神经元死亡和28 d后采用Timm染色检测苔藓纤维发芽状况,并于造模之日起录像监测自发性癫痫的发生。 结果:ICR小鼠经匹罗卡品和红藻氨酸给药后均能诱发出典型的SE,癫痫发作与大鼠和C57/BL6小鼠非常类似,给药后逐渐出现凝视、点头、面部及头部抽搐、全身肌阵挛、跌倒,大、小便失禁及流涎,最终发生全身强直-阵挛性发作、癫痫持续状态。两者Timm染色均能观察到明显的苔藓纤维发芽(P<0.001),且均观测到自发性癫痫的发生,发生几率分别为57.1%和35.7%;戊四氮则表现为间断式的SE,且未见苔藓纤维发芽和自发性癫痫的发生。3种模型均未见明显神经元细胞死亡。 结论:ICR品系小鼠能诱发出与大鼠C57/BL6小鼠类似的癫痫,其中匹罗卡品和红藻氨酸模型是理想的慢性颞叶癫痫模型。ICR品系小鼠作为既经济又有效的模型动物,可常规用于药物筛选和癫痫机制研究。

关 键 词:癫痫/化学诱导  毛果芸香碱/药理学  戊四唑/药理学  红藻氨酸/药理学  疾病模型  动物  匹罗卡品  戊四氮  苔藓纤维发芽  
收稿时间:2013-04-23

Comparison of seizure induced by different drugs in ICR Mice
HU Lin,ZHANG Huadan,CHEN Yatian,HUA Nan,ZENG Linghui.Comparison of seizure induced by different drugs in ICR Mice[J].Journal of Zhejiang University(Medical Sciences),2013,42(6):609-614.
Authors:HU Lin  ZHANG Huadan  CHEN Yatian  HUA Nan  ZENG Linghui
Institution:Zhejiang University City College,School of Medicine,Hangzhou 310015,China
Abstract:Objective: To compare seizure induced by different epileptic drugs in ICR mice. Methods: Male adult ICR mice were injected with pilocarpine (Pilo),kainic acid (KA) and pentylenetetrazole (PTZ) to induce status epilepticus (SE).After 2 h of SE,seizures were terminated by injection of diazepam.Mice were sacrificed and sectioned for assessment of neuronal cell death by Fluro-Jade B staining after 7 d and mossy fiber sprouting by Timm staining after 28 d,respectively.Spontaneous seizures were detected by video for 28 d. Results: Pilo and KA induced typical SE in ICR mice,which was identical to those observed in rats and C57/BL6 mice.Timm staining showed evident mossy fiber sprouting in both Pilo and KA treated mice.The incidences of spontaneous seizure were 57.1% and 35.7% in Pilo and KA treated mice,respectively.Mice treated with PTZ represented kindling model.No mossy fiber sprouting and spontaneous seizures were observed.No cell death was detected in all three groups. Conclusions: Similar seizure pattern is observed in ICR mice as in rats and C57/BL6 mice.Both Pilo and KA model are the ideal models for chronic temporal lobe epilepsy.ICR mice can be widely used as a cheaper substitute in epilepsy research.
Keywords:Epilepsy/chemically induced  Pilocarpine/pharmacology  Pentyleneterazole/pharma-cology  Kainic acid/pharmacology  Didsease models  animal  Pilocarpine  Pentylenetetrazol  Mossy fiber sprouting  
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