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生酮饮食在海马体中表现出神经保护作用,但不能预防成年大鼠内侧颞叶癫痫锂-匹罗卡品模型中的癫痫发生。

Ketogenic diet exhibits neuroprotective effects in hippocampus but fails to prevent epileptogenesis in the lithium-pilocarpine model of mesial temporal lobe epilepsy in adult rats.

机构信息

INSERM U666, Université de Strasbourg; Strasbourg, France.

出版信息

Epilepsia. 2010 Sep;51(9):1829-36. doi: 10.1111/j.1528-1167.2010.02667.x. Epub 2010 Jul 14.

Abstract

PURPOSE

Although the number of antiepileptic drugs (AEDs) is increasing, none displays neuroprotective or antiepileptogenic properties that could prevent status epilepticus (SE)-induced drug-resistant epilepsy. Ketogenic diet (KD) and calorie restriction (CR) are proposed as alternative treatments in epilepsy. Our goal was to assess the neuroprotective or antiepileptogenic effect of these diets in a well-characterized model of mesial temporal lobe epilepsy following initial SE induced by lithium-pilocarpine in adult rats.

METHODS

Seventy-five P50 male Wistar rats were fed a specific diet: normocalorie carbohydrate (NC), hypocalorie carbohydrate (HC), normocalorie ketogenic (NK), or hypocalorie ketogenic (HK). Rats were subjected to lithium-pilocarpine SE, except six NC to constitute a control group for histology (C). Four rats per group were implanted with epidural electrodes to record electroencephalography (EEG) during SE and the next six following days. From the seventh day, the animals were video-recorded 10 h daily to determine latency to epilepsy onset. Neuronal loss in hippocampus and parahippocampal cortices was analyzed 1 month after the first spontaneous seizure.

RESULTS

After lithium-pilocarpine injection, neither KD nor CR modified SE features or latency to epilepsy. In hippocampal layers, KD or CR exhibited a neuroprotective potential without cooperative effect. Parahippocampal cortices were not protected by the diets.

CONCLUSION

The antiepileptic effect of KD and/or CR is overwhelmed by lithium-pilocarpine injection. The isolated protection of hippocampal layers induced by KD or CR or their association failed to modify the course of epileptogenesis.

摘要

目的

尽管抗癫痫药物(AEDs)的数量在不断增加,但没有一种具有神经保护或抗癫痫发生的特性,可以预防癫痫持续状态(SE)引起的耐药性癫痫。生酮饮食(KD)和热量限制(CR)被提议作为癫痫的替代治疗方法。我们的目标是在锂-匹罗卡品诱导的成年大鼠SE 后,通过对内侧颞叶癫痫进行特征明确的模型来评估这些饮食的神经保护或抗癫痫发生作用。

方法

75 只 P50 雄性 Wistar 大鼠喂养特定饮食:正常钙碳水化合物(NC)、低钙碳水化合物(HC)、正常钙生酮(NK)或低钙生酮(HK)。除了 6 只 NC 作为组织学对照(C)组外,所有大鼠均接受锂-匹罗卡品 SE。每组 4 只大鼠植入硬膜外电极以记录 SE 期间和之后 6 天的脑电图(EEG)。从第 7 天开始,动物每天进行 10 小时的视频记录,以确定癫痫发作的潜伏期。在首次自发性癫痫发作后 1 个月分析海马和海马旁皮质中的神经元丢失。

结果

锂-匹罗卡品注射后,KD 或 CR 均未改变 SE 特征或癫痫发作潜伏期。在海马层,KD 或 CR 表现出神经保护潜能,没有协同作用。饮食对海马旁皮质没有保护作用。

结论

KD 和/或 CR 的抗癫痫作用被锂-匹罗卡品注射所掩盖。KD 或 CR 诱导的海马层的单独保护或它们的联合作用未能改变癫痫发生的过程。

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