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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Ketogenic diet protects against epileptogenesis as well as neuronal loss in amygdaloid-kindling seizures
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Ketogenic diet protects against epileptogenesis as well as neuronal loss in amygdaloid-kindling seizures

机译:生酮饮食可防止癫痫发生以及杏仁核样癫痫发作的神经元丢失

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摘要

Ketogenic diets (KD) have shown beneficial effects in terms of anticonvulsant and anti-epileptogenic properties in several experimental models. However, few studies have investigated the consequences of KD with regards to the anti-epileptogenic and neuroprotective effects in kindling-induced seizures. Here, postnatal day 28 male Sprague-Dawley rats received one of two experimental diets for 4 weeks: (a) a 'classic' 4:1 KD; and (b) a normal regular rodent chow diet (ND). Fully-kindled seizures were achieved by daily electrical stimulation in the amygdala. Seizure stage and after-discharge duration (ADD) were assessed daily. The after-discharge threshold (ADT) was measured every 5 days. The effects of the two diets on neuronal loss were observed before kindling and 20 days after stimulation by Nissl staining. We found that the progression of seizure stage and ADD was delayed by KD. KD prevented the ADT decrease on day 5. The incidence of generalized seizures was lower in the KD group compared to the ND group. The neuronal density was decreased in the ipsilateral hilus of the dentate gyrus (DG) and CA1 area, as well as the contralateral CA1 area before kindling in the KD group. However, KD prevented neuronal loss in the ipsilateral CA1 area 20 days after stimulation. Our data suggest that KD can protect against epileptogenesis by preventing both after-discharge generation and propagation in kindling seizures. In addition, KD also possesses a neuroprotective function during kindling although it changes hippocampal development in early life.
机译:在一些实验模型中,生酮饮食(KD)在抗惊厥和抗癫痫发生特性方面显示出有益的作用。但是,很少有研究调查KD在点燃诱发的癫痫发作中的抗癫痫和神经保护作用方面的后果。在这里,出生后第28天的雄性Sprague-Dawley大鼠接受两种实验饮食之一,持续4周:(a)“经典” 4:1 KD; (b)正常的常规啮齿动物饮食(ND)。通过每天在杏仁核中进行电刺激可以完全发作。每天评估癫痫发作阶段和出院后持续时间(ADD)。每5天测量一次放电后阈值(ADT)。在点燃前和尼氏染色刺激后20天观察到两种饮食对神经元丢失的影响。我们发现癫痫发作和ADD的进展被KD延迟了。 KD阻止了ADT在第5天下降。与ND组相比,KD组的全身性癫痫发作发生率更低。在KD组点燃之前,齿状回(DG)和CA1区域的同侧门以及对侧CA1区域的神经元密度降低。然而,KD预防了刺激后20天同侧CA1区域的神经元丢失。我们的数据表明,KD可以通过阻止放电后的产生和点燃癫痫发作的传播来预防癫痫的发生。此外,KD在点燃过程中还具有神经保护功能,尽管它在生命的早期会改变海马的发育。

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