Department of Pharmacology, School of Medicine, Creighton University, Omaha, Nebraska, U.S.A.
Epilepsia. 2014 May;55(5):e44-e49. doi: 10.1111/epi.12603. Epub 2014 Apr 4.
The ketogenic diet (KD) is an effective therapy for pediatric refractory epilepsies; however, whether the KD changes the pathologic network oscillations generated by an epileptic brain remains unknown. We have reported that hippocampal CA3 regions of epileptic Kv1.1α knockout (KO) mice generate pathologic sharp waves (SPWs) and high-frequency oscillations (HFOs) that have higher incidence, longer duration, and fast ripples compared to wild-type (WT). Synaptic activity of hyperexcitable KO mossy fibers significantly decreased CA3 principal cell spike-timing reliability, which contributed to this network pathology. In addition, we have demonstrated that the KD reduces seizures by 75% in KO mice. Here, we determined whether 10- to 14-day in vivo KD treatment exerts disease-modifying effects that alter the spontaneous SPW-HFO complexes generated by the hippocampal CA3 region of KO mice in vitro using extracellular multielectrode array recordings. We found that KD treatment significantly attenuated the pathologic features of KO SPWs and ripples and reduced the incidence of fast ripples. The KD also improved spike-timing reliability of KO CA3 principal cells, decreased mossy fiber excitability, increased mossy fiber-CA3 paired-pulse ratios, and reduced coupling of field excitatory postsynaptic potentials and population spikes in the CA3 region. Collectively, these data indicate that KD treatment modulates CA3-generated pathologic oscillations by dampening hyperactive mossy fiber synapses.
生酮饮食(KD)是治疗儿科难治性癫痫的有效方法;然而,KD 是否改变了癫痫大脑产生的病理网络振荡仍不清楚。我们已经报道,癫痫 Kv1.1α 敲除(KO)小鼠的海马 CA3 区产生病理尖波(SPW)和高频振荡(HFO),与野生型(WT)相比,其发生率更高、持续时间更长、快涟漪更快。兴奋性过高的 KO 苔藓纤维的突触活动显著降低了 CA3 主细胞的尖峰定时可靠性,这导致了这种网络病理学。此外,我们已经证明 KD 可使 KO 小鼠的癫痫发作减少 75%。在这里,我们使用细胞外多电极阵列记录确定了 10-14 天的体内 KD 治疗是否会产生疾病修饰作用,从而改变 KO 小鼠海马 CA3 区自发产生的 SPW-HFO 复合物。我们发现 KD 治疗显著减弱了 KO SPW 和涟漪的病理特征,并降低了快涟漪的发生率。KD 还改善了 KO CA3 主细胞的尖峰定时可靠性,降低了苔藓纤维兴奋性,增加了苔藓纤维-CA3 成对脉冲比,并减少了 CA3 区的场兴奋性突触后电位和群体峰的耦合。总的来说,这些数据表明 KD 治疗通过抑制过度活跃的苔藓纤维突触来调节 CA3 产生的病理振荡。