Ketogenic diet attenuates neuroinflammation and restores hippocampal neurogenesis to improve CUMS induced depression-like behavior in mice

IF 5.4 1区 农林科学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Food & Function Pub Date : 2025-03-29 DOI:10.1039/D5FO00226E
Jinyuan Liang, Jingxi Zhang, Jingyu Sun, Qingsheng Liang, Yingtong Zhan, Zhiyou Yang, Yongping Zhang, Leigang Jin, Chuanyin Hu and Yun-Tao Zhao
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Abstract

The ketogenic diet (KD) has been proposed as a potential treatment for depression. However, the underlying mechanisms remain poorly understood. This study aimed to evaluate further the effects of KD on chronic unpredictable mild stress (CUMS)-induced depression in mice and investigate the underlying mechanisms. The results demonstrated that KD intervention significantly alleviated CUMS-induced depression-like behaviors, as evidenced by a decrease in immobility time in the forced swimming test and tail suspension test, an increase in distance traveled in the open field test, and a greater preference for sucrose in the sucrose preference test. KD alleviated neuroinflammation by reducing the levels of glial cell activation markers Iba-1 and GFAP, inhibiting the expression of inflammatory factors IL-1β, TNF-α, and COX-2, and suppressing the overactivation of the TLR4/MyD88/NF-κB signaling pathway. Furthermore, KD increased the number of DCX-, BrdU-, and PSD95-positive cells in the hippocampus and enhanced the BDNF/TrkB/CREB and Wnt/β-catenin signaling pathways, thereby promoting hippocampal neurogenesis. These findings suggested that KD alleviated CUMS-induced depression-like behaviors in mice by reducing neuroinflammation, enhancing neurotrophic signaling, and promoting hippocampal neurogenesis, thereby providing a mechanistic basis for its potential as a novel dietary antidepressant therapy.

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生酮饮食减轻神经炎症,恢复海马神经发生,以改善小鼠CUMS诱导的抑郁样行为。
生酮饮食(KD)被认为是一种潜在的治疗抑郁症的方法。然而,潜在的机制仍然知之甚少。本研究旨在进一步评估KD对小鼠慢性不可预测轻度应激(CUMS)诱导的抑郁症的影响,并探讨其潜在机制。结果表明,KD干预显著缓解了coms诱导的抑郁样行为,表现为强迫游泳试验和悬尾试验中静止时间减少,开阔场地试验中行走距离增加,蔗糖偏好试验中对蔗糖的偏好增加。KD通过降低胶质细胞活化标志物Iba-1和GFAP的水平,抑制炎症因子IL-1β、TNF-α和COX-2的表达,抑制TLR4/MyD88/NF-κB信号通路的过度激活,从而减轻神经炎症。此外,KD增加海马中DCX-、BrdU-和psd95阳性细胞数量,增强BDNF/TrkB/CREB和Wnt/β-catenin信号通路,从而促进海马神经发生。这些研究结果表明,KD通过减少神经炎症、增强神经营养信号和促进海马神经发生来减轻小鼠cms诱导的抑郁样行为,从而为其作为一种新型饮食抗抑郁药物的潜力提供了机制基础。
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来源期刊
Food & Function
Food & Function BIOCHEMISTRY & MOLECULAR BIOLOGY-FOOD SCIENCE & TECHNOLOGY
CiteScore
10.10
自引率
6.60%
发文量
957
审稿时长
1.8 months
期刊介绍: Food & Function provides a unique venue for physicists, chemists, biochemists, nutritionists and other food scientists to publish work at the interface of the chemistry, physics and biology of food. The journal focuses on food and the functions of food in relation to health.
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