生酮饮食对癫痫持续状态大鼠认知障碍的保护作用:通过NF-κB信号通路调节神经炎症。

Pediatric discovery Pub Date : 2025-06-23 eCollection Date: 2025-06-01 DOI:10.1002/pdi3.70013
Wandi Wang, Lingman Wang, Chunxue Jiang, Shengxuan Zhang, Chen Tan, Liqiong Peng, Ran Ding, Bing Tian, Xiaojie Song, Li Jiang
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引用次数: 0

摘要

癫痫是一种慢性神经系统疾病,其特征是异常同步的神经元放电,导致认知功能障碍。生酮饮食(KD)有望成为一种有效治疗耐药癫痫(DRE)的方法,可以减少癫痫发作,改善患者的认知和行为结果。然而,确切的神经保护机制尚不完全清楚。本研究旨在探讨KD对癫痫持续状态(SE)大鼠认知功能障碍和海马神经回路损伤的影响,重点关注核因子κB (NF-κB)信号通路。匹罗卡品诱导SE,将大鼠分为KD组和对照组。KD治疗7天和20天后,通过高架+迷宫、Morris水迷宫、新物体识别和y迷宫测试评估认知功能。分析海马组织神经回路结构损伤情况。western blot和免疫荧光法检测NF-κB通路活化情况。结果表明,KD显著提高认知能力,减少海马损伤。此外,KD抑制NF-κB通路的激活,其证据是NF-κB、p- i -κB和促炎细胞因子水平的降低。这些研究结果表明,KD可能通过调节NF-κB信号传导来减轻认知缺陷和海马损伤,为其神经保护机制和作为癫痫替代治疗的潜力提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective Effects of the Ketogenic Diet on Cognitive Impairment Induced by Status Epilepticus in Rats: Modulation of Neuroinflammation Through the NF-κB Signaling Pathway.

Epilepsy is a chronic neurological disorder characterized by abnormal synchronized neuronal discharges, leading to cognitive dysfunction. The ketogenic diet (KD) has shown promise as an effective treatment for drug-resistant epilepsy (DRE), reducing seizures and improving cognitive and behavioral outcomes in patients. However, the precise neuroprotective mechanisms are not fully understood. This study aimed to investigate the effects of KD on cognitive impairment and hippocampal neurocircuit damage in rats with status epilepticus (SE), with a focus on a nuclear factor-kappa B (NF-κB) signaling. SE was induced using pilocarpine, and rats were assigned to KD and control groups. After 7 and 20 days of KD treatment, cognitive function was assessed using the elevated plus-maze, Morris water maze, novel object recognition, and Y-maze tests. Hippocampal tissue was analyzed for structural damage of neurocircuit. NF-κB pathway activation was evaluated by western blot and immunofluorescence. Results indicated that KD significantly improved cognitive performance and reduced hippocampal damage. Additionally, KD inhibited NF-κB pathway activation, evidenced by decreased levels of NF-κB, p-IκB, and proinflammatory cytokines. These findings suggest that KD may alleviate cognitive deficits and hippocampal damage by modulating the NF-κB signaling, providing insights into its neuroprotective mechanisms and potential as an alternative treatment for epilepsy.

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