Neural Regeneration Research ›› 2023, Vol. 18 ›› Issue (12): 2767-2772.doi: 10.4103/1673-5374.373715

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Ketogenic diet alleviates cognitive dysfunction and neuroinflammation in APP/PS1 mice via the Nrf2/HO-1 and NF-κB signaling pathways

Jingwen Jiang1, Hong Pan1, Fanxia Shen1, Yuyan Tan1, *, Shengdi Chen1, 2, *   

  1. 1Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; 2Lab of Translational Research of Neurodegenerative Diseases, Institute of Immunochemistry, ShanghaiTech University, Shanghai, China
  • Online:2023-12-15 Published:2023-06-16
  • Contact: Shengdi Chen, PhD, MD, chensd@rjh.com.cn; Yuyan Tan, PhD, MD, tyy11672@rjh.com.cn.
  • Supported by:
    This work was supported by the National Natural Science Foundation of China, Nos. 82171401, 81971187 (to SC), and 81971183 (to YT), grants from Shanghai Municipal Science and Technology Major Project, No. 2018SHZDZX05 (to SC) and Shanghai Municipal Education Commission, No. 2017-01-07-00-01-E00046 (to SC). 

Abstract: Alzheimer’s disease is a progressive neurological disorder characterized by cognitive decline and chronic inflammation within the brain. The ketogenic diet, a widely recognized therapeutic intervention for refractory epilepsy, has recently been proposed as a potential treatment for a variety of neurological diseases, including Alzheimer’s disease. However, the efficacy of ketogenic diet in treating Alzheimer’s disease and the underlying mechanism remains unclear. The current investigation aimed to explore the effect of ketogenic diet on cognitive function and the underlying biological mechanisms in a mouse model of Alzheimer’s disease. Male amyloid precursor protein/presenilin 1 (APP/PS1) mice were randomly assigned to either a ketogenic diet or control diet group, and received their respective diets for a duration of 3 months. The findings show that ketogenic diet administration enhanced cognitive function, attenuated amyloid plaque formation and proinflammatory cytokine levels in APP/PS1 mice, and augmented the nuclear factor-erythroid 2-p45 derived factor 2/heme oxygenase-1 signaling pathway while suppressing the nuclear factor-kappa B pathway. Collectively, these data suggest that ketogenic diet may have a therapeutic potential in treating Alzheimer’s disease by ameliorating the neurotoxicity associated with Aβ-induced inflammation. This study highlights the urgent need for further research into the use of ketogenic diet as a potential therapy for Alzheimer’s disease.

Key words: Alzheimer’s disease, APP/PS1 mice, cognitive impairment, ketogenic diet, neuroinflammation, nuclear factor-kappa B pathway, nuclear factor-erythroid 2-p45 derived factor 2/heme oxygenase-1, therapeutic benefits