Xu Xiang-ping, Erichsen Daniel, Börjesson Sara I, Dahlin Maria, Amark Per, Elinder Fredrik
Department of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, SE-581 85 Linköping, Sweden.
Epilepsy Res. 2008 Jul;80(1):57-66. doi: 10.1016/j.eplepsyres.2008.03.013. Epub 2008 May 2.
Many children with epilepsy do not satisfactorily respond to conventional pharmacological therapy, but to the ketogenic diet, a high-fat, low-carbohydrate diet. This diet increases the concentrations of ketone bodies and polyunsaturated fatty acids (PUFAs) in cerebrospinal fluid (CSF) and plasma. However, its anticonvulsant mechanism is not known.
To investigate the mechanism by which the diet protects against seizures, we studied the effects of several PUFAs (docosahexaenoic acid, eicosapentaenoic acid, and linoleic acid), ketone bodies (beta-hydroxybuturic acid and acetoacetic acid), and CSF from patients on the ketogenic diet on the voltage-gated Shaker K channel expressed in Xenopus oocytes.
We found that PUFAs at concentrations down to 21microM clearly increased the K current by shifting the conductance versus voltage curve in negative direction along the voltage axis. CSF from patients on the ketogenic diet has similar but smaller effects. In contrast, high concentrations (1-5mM) of ketone bodies did not affect the K current. Computer simulations showed that the observed shifts for clinically relevant concentrations of PUFAs, and CSF from patients could effectively impair repetitive firing.
These data suggest that the ketogenic diet could prevent epileptic seizures by PUFA-induced openings of voltage-gated K channels.
许多癫痫患儿对传统药物治疗反应不佳,但对生酮饮食(一种高脂肪、低碳水化合物饮食)有反应。这种饮食会增加脑脊液(CSF)和血浆中酮体和多不饱和脂肪酸(PUFA)的浓度。然而,其抗惊厥机制尚不清楚。
为了研究该饮食预防癫痫发作的机制,我们研究了几种多不饱和脂肪酸(二十二碳六烯酸、二十碳五烯酸和亚油酸)、酮体(β-羟基丁酸和乙酰乙酸)以及生酮饮食患者的脑脊液对非洲爪蟾卵母细胞中表达的电压门控Shaker K通道的影响。
我们发现,低至21微摩尔浓度的多不饱和脂肪酸通过使电导与电压曲线沿电压轴负向移动,明显增加了钾电流。生酮饮食患者的脑脊液有类似但较小的作用。相比之下,高浓度(1 - 5毫摩尔)的酮体不影响钾电流。计算机模拟表明,观察到的临床相关浓度的多不饱和脂肪酸和患者脑脊液的变化可有效损害重复放电。
这些数据表明,生酮饮食可能通过多不饱和脂肪酸诱导电压门控钾通道开放来预防癫痫发作。