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构建海人酸诱导的内侧颞叶癫痫小鼠模型 被引量:2

Establishment of kainic acid-induced mice models of medial temporal lobe epilepsy
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摘要 目的建立C57BL/6颞叶癫痫小鼠模型,观察其在行为学和病理学上的变化。方法将C57BL/6小鼠随机分为空白对照组、0.9%氯化钠注射组(35μL/g)和海人酸注射组(12 mg/kg),进行单侧海马注射。注射5 d或5周后,取小鼠脑进行HE染色,观察海马病理结构改变;检测海马组织中mTOR通路标志物P-S6蛋白质表达量的改变。结果 (1)海人酸注射小鼠发生面部抽搐、双侧前肢痉挛等急性期癫痫持续发作和慢性期自发发作;(2)海马注射侧CA1、CA3神经元明显丢失,慢性期小鼠模型出现中齿状回颗粒细胞散布,符合海马硬化特征性病理改变;(3)小鼠海马组织中P-S6蛋白质的表达量在急性期(P<0.05)和慢性期(P<0.01)均上调。结论单侧海马注射海人酸可成功建立C57BL/6小鼠内侧颞叶癫痫模型,可观察到与内侧颞叶癫痫临床表现类似的行为学、组织病理学上的改变。 Objective To establish the kainic acid(KA)-induced mesial temporal lobe epilepsy(TLE) mice model and detect the characteristic changes.Methods Healthy male C57BL/6 mice were randomly divided into control group(non-injected),saline group(35 μL/g) and KA group(12 mg/kg) for intrahippocampal injections.5 days and 5 weeks after injection,the mice brains were sectioned and stained by hemotoxylin-eosin(HE) to detect the pathologic changes in the hippocampal area;the expression level of P-S6 protein,the marker of hippocampus mTOR signal pathway,was also determinated to verify the animal model.Results(1)Only KA-treated mice showed wet dog shakes,facial clonus and generalized tonic-clonic convulsions.(2)After injection of KA,neuronal cell loss was prominent in in CA1,CA3 and hilar area of the ipsilateral hippocampus;granule cell in dentate gyrus area dispersed,which are fertures of hippocampus sclerosis.(3)P-S6 expression level increased in both acute(P0.05) and chronic phases(P0.01) of MTLE models.Conclusion Intrahippocampal injection of KA inC57BL/6 mice could induce behavioural,histopathological changes which are similar to those clinic features of MTLE.
出处 《基础医学与临床》 CSCD 北大核心 2011年第7期820-826,共7页 Basic and Clinical Medicine
基金 国家自然科学基金(30971001 30721063) 北京自然科学基金(7102109) 霍英东教育基金(121024)
关键词 内侧颞叶癫痫 海人酸 C57BL/6小鼠 海马硬化 mesial temporal lobe epilepsy kainic acid C57BL/6 mice hippocampus sclerosis
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