Crotts Megan S, Kim YuJaung, Bravo Eduardo, Richerson George B, Teran Frida A
Department of Neurology, University of Iowa, Iowa City, IA 52242, United States; Iowa Neuroscience Institute, University of Iowa, Iowa City, IA 52242, United States.
Department of Neurology, University of Iowa, Iowa City, IA 52242, United States.
Epilepsy Behav. 2021 Sep 29;124:108334. doi: 10.1016/j.yebeh.2021.108334.
Patients with uncontrolled epilepsy have a high risk of sudden unexpected death in epilepsy (SUDEP). Seizure-induced respiratory arrest (S-IRA) is thought to be the determining cause of death in many cases of SUDEP. The goal of the present study was to use Scn1a (Dravet Syndrome, DS) and DBA/1 mice to determine: (1) the effect of a ketogenic diet (KD) on S-IRA and (2) the relationship between serum ketones and the protective effect of a KD. Ketogenic diet treatment significantly decreased spontaneous seizure-induced mortality in DS mice compared to control (8% vs 39%, p = 0.0021). This protective effect was not abolished when ketosis was prevented by supplementing the KD with glucose (10% mortality, p = 0.0007). In DBA/1 mice, the latency to onset of S-IRA due to audiogenic seizures was delayed from 7.6 to 20.8 seconds by a KD on treatment day (TD) 7 compared to control (p < 0.0001), an effect that was reversed on TD14 when mice were crossed over to a control diet on TD7. β-Hydroxybutyrate (BHB) levels were significantly decreased in DBA/1 mice on a KD supplemented with glucose (p = 0.0038), but the protective effect was maintained. Our findings show that a KD decreases SUDEP in DS mice and increases the latency to audiogenic S-IRA in DBA/1 mice. In both mouse models, a KD was protective against S-IRA. This effect may be due in part to specific dietary components rather than generation of ketone bodies.
癫痫控制不佳的患者发生癫痫猝死(SUDEP)的风险很高。癫痫发作诱发的呼吸骤停(S-IRA)被认为是许多SUDEP病例中的决定性死因。本研究的目的是使用Scn1a(德雷维特综合征,DS)和DBA/1小鼠来确定:(1)生酮饮食(KD)对S-IRA的影响,以及(2)血清酮与KD保护作用之间的关系。与对照组相比,生酮饮食治疗显著降低了DS小鼠自发癫痫发作导致的死亡率(8%对39%,p = 0.0021)。当通过在KD中添加葡萄糖来预防酮症时,这种保护作用并未消除(死亡率为10%,p = 0.0007)。在DBA/1小鼠中,与对照组相比,在治疗第7天(TD),KD使由听源性癫痫发作引起的S-IRA发作潜伏期从7.6秒延长至20.8秒(p < 0.0001),当小鼠在TD7转而采用对照饮食时,这种作用在TD14时逆转。在添加葡萄糖的KD喂养的DBA/1小鼠中,β-羟基丁酸(BHB)水平显著降低(p = 0.0038),但保护作用得以维持。我们的研究结果表明,KD可降低DS小鼠的SUDEP,并增加DBA/1小鼠对听源性S-IRA的潜伏期。在两种小鼠模型中,KD均对S-IRA具有保护作用。这种作用可能部分归因于特定的饮食成分,而非酮体的生成。