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热量限制的生酮饮食提高了对戊四氮诱发的所有癫痫发作模式的阈值:电临床评估的关键重要性。

Calorie-restricted ketogenic diet increases thresholds to all patterns of pentylenetetrazol-induced seizures: critical importance of electroclinical assessment.

作者信息

Raffo Emmanuel, François Jennifer, Ferrandon Arielle, Koning Estelle, Nehlig Astrid

机构信息

INSERM U 666, 67085 Strasbourg, France.

出版信息

Epilepsia. 2008 Feb;49(2):320-8. doi: 10.1111/j.1528-1167.2007.01380.x. Epub 2007 Oct 15.

Abstract

PURPOSE

Thresholds to pentylenetetrazol (PTZ) seizures were usually based only on clinical symptoms. Our purpose was to use electroclinical patterns to assess the efficacy of a ketogenic and/or calorie-restricted diet on PTZ-induced seizures.

METHODS

Forty 50-day-old rats were divided in four weight-matched groups and fed controlled diets: normocalorie carbohydrate (NC), hypocalorie carbohydrate (HC), normocalorie ketogenic (NK), and hypocalorie ketogenic (HK). After 21 days, blood glucose and beta-hydroxybutyrate levels were determined and seizures were induced by continuous infusion of PTZ. The clinical and EEG thresholds to each seizure pattern were compared between the different groups.

RESULTS

The electroclinical course of PTZ-induced seizures was similar in all groups. The HK group exhibited higher thresholds than the other ones for most clinical features: absence (p = 0.003), first overt myoclonia (p = 0.028), clonic seizure (p = 0.006), and for EEG features: first spike (p = 0.036), first spike-and-wave discharge (p = 0.014), subcontinuous spike-and-wave discharges (p = 0.005). NK, HC, and NC groups were not significantly different from each other. Blood glucose and beta-hydroxybutyrate levels were not correlated with electroclinical seizure thresholds. After the clonic seizure, despite stopping PTZ infusion, a tonic seizure occurred in some animals, without significant difference regarding the diet.

CONCLUSION

This approach permitted a precise study of the electroclinical course of PTZ-induced seizures. In addition to the usually studied first overt myoclonia, we clearly demonstrated the efficiency of a calorie restricted KD in elevating thresholds to most electroclinical seizure patterns. We confirmed the lack of efficiency of the KD to reduce seizure severity once the seizure has started.

摘要

目的

戊四氮(PTZ)诱发癫痫的阈值通常仅基于临床症状。我们的目的是利用电临床模式评估生酮和/或热量限制饮食对PTZ诱发癫痫的疗效。

方法

将40只50日龄大鼠分为四个体重匹配组,给予不同的对照饮食:正常热量碳水化合物(NC)组、低热量碳水化合物(HC)组、正常热量生酮(NK)组和低热量生酮(HK)组。21天后,测定血糖和β-羟基丁酸水平,并通过持续输注PTZ诱发癫痫。比较不同组之间每种癫痫发作模式的临床和脑电图阈值。

结果

所有组中PTZ诱发癫痫的电临床过程相似。HK组在大多数临床特征方面的阈值高于其他组:失神发作(p = 0.003)、首次明显肌阵挛(p = 0.028)、阵挛性发作(p = 0.006),以及脑电图特征方面:首次棘波(p = 0.036)、首次棘慢波发放(p = 0.014)、亚持续性棘慢波发放(p = 0.005)。NK组、HC组和NC组之间无显著差异。血糖和β-羟基丁酸水平与电临床癫痫阈值无关。阵挛性发作后,尽管停止输注PTZ,但一些动物仍出现强直性发作,不同饮食组之间无显著差异。

结论

这种方法允许对PTZ诱发癫痫的电临床过程进行精确研究。除了通常研究的首次明显肌阵挛外,我们清楚地证明了热量限制的生酮饮食在提高大多数电临床癫痫发作模式阈值方面的有效性。我们证实,一旦癫痫发作开始,生酮饮食在降低癫痫严重程度方面缺乏有效性。

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