Ketogenic diet-induced extension of longevity in epileptic Kcna1-null mice is influenced by gender and age at treatment onset

被引:14
作者
Chun, Kyoung-chul [1 ,2 ,3 ,4 ]
Ma, Shun-Chieh [1 ,2 ]
Oh, Hyoungil [1 ,2 ]
Rho, Jong M. [5 ,6 ,7 ]
Kim, Do Young [1 ,2 ]
机构
[1] St Josephs Hosp, Barrow Neurol Inst, Dept Neurobiol, Phoenix, AZ USA
[2] St Josephs Hosp, Barrow Neurol Inst, Dept Neurol, Phoenix, AZ USA
[3] Inje Univ, Ilsan Paik Hosp, Coll Med, Dept Obstet, Gyeonggi, South Korea
[4] Inje Univ, Ilsan Paik Hosp, Coll Med, Dept Gynecol, Gyeonggi, South Korea
[5] Univ Calgary, Cumming Sch Med, Alberta Childrens Hosp Res Inst, Dept Pediat, Calgary, AB, Canada
[6] Univ Calgary, Cumming Sch Med, Alberta Childrens Hosp Res Inst, Dept Clin Neurosci, Calgary, AB, Canada
[7] Univ Calgary, Cumming Sch Med, Alberta Childrens Hosp Res Inst, Dept Physiol & Pharmacol, Calgary, AB, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
Ketogenic diet; Epilepsy; Longevity; Kcnal-null mice; SUDEP; Gender; Treatment; SUDDEN UNEXPECTED DEATH; RISK-FACTORS; MOUSE;
D O I
10.1016/j.eplepsyres.2017.11.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Sudden unexpected death in epilepsy (SUDEP) is a leading cause of premature mortality in patients with epilepsy, and has been linked to multiple risk factors, including gender and early age at seizure onset. Despite the lack of a targeted therapy for SUDEP, it has recently been shown that a high-fat, low carbohydrate ketogenic diet (KD) enhances longevity in the epileptic Kcnal-null (KO) mouse, a validated model of SUDEP. Here, we asked whether the KD-driven prolongation of lifespan in KO mice is dependent on sex and/or age at treatment onset. We found that as KO mice aged, their daily seizure frequency steadily increased, but had early demise by postnatal day (PD) 46.9 +/- 0.8. In KO mice started on the KD at PD30, longevity was extended to a mean of PD 69.8 +/- 1.7, accompanied with improved seizure control. Interestingly, while seizure control on the KD was similar between male and female mice, KD-fed female KO mice survived longer than their male counterparts. Further, epileptic mice initiated on the KD at PD25 had longer lifespans compared to those placed on the KD starting at PD35. Collectively, these data further support the notion that the KD can retard disease progression and sudden death in KO mice, but that this beneficial action is influenced by gender and age at the start of treatment.
引用
收藏
页码:53 / 55
页数:3
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