Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Neurosci Lett. 2012 Feb 2;508(1):22-6. doi: 10.1016/j.neulet.2011.12.002. Epub 2011 Dec 13.
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.
生酮饮食(KD)在多种实验模型中显示出抗惊厥和抗癫痫发生的有益作用。然而,很少有研究调查 KD 对点燃诱导的癫痫发作的抗癫痫发生和神经保护作用的后果。在这里,雄性 Sprague-Dawley 大鼠在出生后第 28 天接受了两种实验饮食中的一种,持续 4 周:(a)“经典”4:1 KD;和(b)正常的常规啮齿动物饲料饮食(ND)。通过在杏仁核中进行每日电刺激来实现完全点燃的癫痫发作。每日评估癫痫发作阶段和发作后放电持续时间(ADD)。每隔 5 天测量发作后放电阈值(ADT)。通过尼氏染色在点燃前和刺激后 20 天观察两种饮食对神经元丢失的影响。我们发现 KD 延迟了癫痫发作阶段和 ADD 的进展。KD 预防了 ADT 在第 5 天的下降。与 ND 组相比,KD 组全身性癫痫发作的发生率较低。在 KD 组中,在点燃之前,同侧齿状回(DG)和 CA1 区的神经细胞密度以及对侧 CA1 区的神经细胞密度降低。然而,KD 预防了刺激后 20 天同侧 CA1 区的神经元丢失。我们的数据表明,KD 可以通过防止点燃性癫痫发作中的发作后放电的产生和传播来保护癫痫发生。此外,KD 在点燃期间还具有神经保护作用,尽管它改变了生命早期的海马发育。