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生酮饮食对电刺激杏仁核点燃诱导癫痫发作的雄性大鼠齿状回和CA3区KCC2表达的影响。

Effects of the ketogenic diet on dentate gyrus and CA3 KCC2 expression in male rats with electrical amygdala kindling-induced seizures.

作者信息

Granados-Rojas Leticia, Hernández-López Leonardo, Bahena-Alvarez Emmanuel Leonardo, Juárez-Zepeda Tarsila Elizabeth, Custodio Verónica, Martínez-Galindo Joyce Graciela, Jerónimo-Cruz Karina, Tapia-Rodríguez Miguel, Vanoye-Carlo America, Duran Pilar, Rubio Carmen

机构信息

Laboratorio de Biomoléculas y Salud Infantil, Instituto Nacional de Pediatría, Mexico City, Mexico.

Departamento de Neurofisiología, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.

出版信息

Front Neurosci. 2025 Apr 8;19:1489407. doi: 10.3389/fnins.2025.1489407. eCollection 2025.

Abstract

INTRODUCTION

Ketogenic diet (KD), a high-fat, low-carbohydrate, and adequate protein diet, is a non-pharmacological treatment for refractory epilepsy. However, their mechanism of action is not fully understood. The cation-chloride cotransporter, KCC2, transports chloride out of neurons, thus contributing to the intraneuronal concentration of chloride. Modifications in KCC2 expression by KD feeding could explain the beneficial effect of this diet on epilepsy. This study aimed to determine the impact of KD on KCC2 expression in dentate gyrus layers and Cornu Ammonis 3 (CA3) strata of rats with seizures induced by amygdaloid kindling.

MATERIALS AND METHODS

Male Sprague Dawley rats were fed a normal diet (ND) or KD from postnatal day 24 until the end of the experiment. At 6 weeks after the start of the diets, rats were subjected to an amygdala kindling epilepsy model, sham or remain intact. Glucose and β-hydroxybutyrate concentrations were quantified. The after-discharge duration (ADD), latency, and duration of stages of kindling were evaluated. In addition, KCC2 expression was evaluated using optical density. A Pearson bivariate correlation was used to determine the relationship between KCC2 expression and ADD.

RESULTS

At the end of the experiment, the KD-fed groups showed a reduction in glucose and an increase in β-hydroxybutyrate. KD reduced ADD and increased latency and duration of generalized seizures. In ND-fed animals, kindling reduced KCC2 expression in all three layers of the dentate gyrus; however, in KD-fed animals, no changes were observed. KD treatment increased KCC2 expression in the kindling group. In CA3, the pyramidal and lucidum strata showed an increase of KCC2 in KD-fed groups. Besides, the kindling had lower levels of KCC2 than the sham and intact groups. In all layers of the dentate gyrus and pyramidal and lucidum CA3 strata, the correlation indicated that the higher the KCC2 expression, the shorter the ADD during generalized seizures.

CONCLUSION

KD reduces ADD in generalized seizures. In addition, KD has a putative neuroprotective effect by preventing the kindling-induced reduction of KCC2 expression in the molecular, granule, and hilar dentate gyrus layers and pyramidal and lucidum CA3 strata. Increased KCC2 expression levels are related to a shorter duration of generalized seizures.

摘要

引言

生酮饮食(KD)是一种高脂肪、低碳水化合物且蛋白质含量充足的饮食,是治疗难治性癫痫的一种非药物疗法。然而,其作用机制尚未完全明确。阳离子 - 氯离子共转运体KCC2将氯离子转运出神经元,从而影响神经元内氯离子浓度。通过生酮饮食喂养对KCC2表达的改变可能解释了这种饮食对癫痫的有益作用。本研究旨在确定生酮饮食对杏仁核点燃诱导癫痫发作的大鼠齿状回层和海马体3(CA3)层中KCC2表达的影响。

材料与方法

雄性Sprague Dawley大鼠从出生后第24天开始喂食正常饮食(ND)或生酮饮食,直至实验结束。在饮食开始6周后,将大鼠分为杏仁核点燃癫痫模型组、假手术组或完整组。对葡萄糖和β - 羟基丁酸浓度进行定量分析。评估后放电持续时间(ADD)、潜伏期以及点燃各阶段的持续时间。此外,使用光密度评估KCC2表达。采用Pearson双变量相关性分析来确定KCC2表达与ADD之间的关系。

结果

在实验结束时,喂食生酮饮食的组葡萄糖水平降低,β - 羟基丁酸水平升高。生酮饮食减少了ADD,并增加了全身性癫痫发作的潜伏期和持续时间。在喂食正常饮食的动物中,点燃降低了齿状回所有三层中的KCC2表达;然而,在喂食生酮饮食的动物中,未观察到变化。生酮饮食治疗使点燃组的KCC2表达增加。在CA3区,锥体层和透明层在喂食生酮饮食的组中KCC2增加。此外,点燃组的KCC2水平低于假手术组和完整组。在齿状回的所有层以及CA3区的锥体层和透明层中,相关性表明KCC2表达越高,全身性癫痫发作期间的ADD越短。

结论

生酮饮食可减少全身性癫痫发作的ADD。此外,生酮饮食通过防止在分子层、颗粒层和齿状回门区以及CA3区的锥体层和透明层中点燃诱导的KCC2表达降低,具有潜在的神经保护作用。KCC2表达水平的增加与全身性癫痫发作持续时间缩短有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/560c/12011780/f7ec321095cd/fnins-19-1489407-g001.jpg

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