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首页> 外文期刊>Brain research >Topiramate reduces blood-brain barrier disruption and inhibits seizure activity in hyperthermia-induced seizures in rats with cortical dysplasia
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Topiramate reduces blood-brain barrier disruption and inhibits seizure activity in hyperthermia-induced seizures in rats with cortical dysplasia

机译:托吡酯可减少皮层异常增生大鼠在热疗诱发的癫痫发作中的血脑屏障破坏并抑制癫痫发作活动

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We investigated the effects of topiramate (TPM), a novel broad spectrum anticonvulsant, on seizure severity, survival rate and blood-brain barrier (BBB) integrity during hyperthermic seizures in rats with cortical dysplasia (CD). Offsprings of irradiated mothers were used in this study. To show the functional and morphological alterations in BBB integrity, quantitative analysis of Evans blue (EB) extravasation, immunohistochemistry and electron microscopic assessment of horseradish peroxidase (HRP) permeability were performed. Rats with CD exposed to hyperthermia exhibited seizures with mean Racine's scores of 3.92??1.2. Among the rats with CD pretreated with TPM, 21 of 24 rats showed no sign of seizure activity upon exposure to hyperthermia (p<0.01). The immunoreactivity of occludin, a tight junction protein, remained essentially unaltered in capillaries of hippocampus in all groups. In animals with CD exposed to hyperthermia, the significantly increased p-glycoprotein immunoreactivity in hippocampus (p<0.01) was slightly decreased by TPM pretreatment. Hyperthermic seizures increased BBB permeability to EB in animals with CD, but TPM pretreatment decreased the penetration of the tracer into the brain in these animals (p<0.01). Ultrastructurally frequent vesicles containing HRP reaction products were observed in capillary endothelial cells in cerebral cortex and hippocampus of rats with CD subjected to hyperthermia-induced seizures, and TPM pretreatment prevented the development of HRP reaction products in these animals. The results of this study suggest that TPM inhibits seizure activity and maintains BBB integrity in the course of febrile seizures in the setting of CD. ? 2012 Elsevier B.V.
机译:我们调查了皮质异型增生(CD)大鼠高热惊厥过程中新型广谱抗惊厥药托吡酯(TPM)对癫痫发作严重程度,存活率和血脑屏障(BBB)完整性的影响。在这项研究中使用了受辐照母亲的后代。为了显示BBB完整性的功能和形态变化,进行了伊文思蓝(EB)外渗的定量分析,免疫组化和辣根过氧化物酶(HRP)渗透性的电子显微镜评估。 CD暴露于高热的大鼠表现出癫痫发作,平均Racine评分为3.92≤1.2。在接受TPM预处理的CD大鼠中,有24只大鼠中有21只在暴露于高热时没有癫痫发作的迹象(p <0.01)。在所有组中,紧密连接蛋白occludin的免疫反应性基本上保持不变。在CD暴露于高温的动物中,TPM预处理可稍微降低海马中p-糖蛋白免疫反应性的显着增加(p <0.01)。在患有CD的动物中,高热惊厥增加了BBB对EB的通透性,但是TPM预处理降低了这些动物中示踪剂向大脑的渗透(p <0.01)。在热疗性癫痫发作的CD大鼠的大脑皮层和海马毛细血管内皮细胞中观察到含有HRP反应产物的超微结构囊泡,而TPM预处理阻止了这些动物中HRP反应产物的发展。这项研究的结果表明,在CD的背景下,高热惊厥过程中TPM抑制了癫痫发作的活动并保持了BBB的完整性。 ? 2012年Elsevier B.V.

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