Ketogenic diet alleviates brain iron deposition and cognitive dysfunction via Nrf2-mediated ferroptosis pathway in APP/PS1 mouse

Brain Res. 2023 Aug 1:1812:148404. doi: 10.1016/j.brainres.2023.148404. Epub 2023 May 8.

Abstract

Progressive cognitive decline and increased brain iron deposition with age are important features of Alzheimer's disease. Previous studies have found that the short-term ketogenic diet has neuroprotective effects in a variety of neurodegenerative diseases, but the effects of an early and long-term ketogenic diet on brain iron content and cognition of Alzheimer's disease have not been reported. In our study, 8-week-old APP/PS1 mice were given a 12-month ketogenic or standard diet, while C57BL/6 mice matched with the age and genetic background of APP/PS1 mice were used as normal controls to be given a standard diet for the same length of time. We found that 12 months of an early ketogenic diet improved the impaired learning and memory ability of APP/PS1 mice. The improvement of cognitive function may be related to the reduction of amyloid-beta deposition and neuronal ferroptosis. The mechanism was achieved by the regulation of ferroptosis-related pathways after activation of nuclear factor erythroid 2-related factor 2 by ketogenic diet-induced elevated β-hydroxybutyrate. In addition, blood biochemical results showed that compared with the standard diet group of the disease, although the early and long-term ketogenic diet increased blood lipids to some extent, it seemed to reduce liver, renal, and myocardial damage caused by genetic differences. This will provide a piece of positive evidence for the early and long-term use of ketogenic diets in people at risk of Alzheimer's disease.

Keywords: Alzheimer's disease; Brain iron deposition; Cognitive dysfunction; Ferroptosis; Ketogenic diet.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease* / metabolism
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism
  • Animals
  • Brain / metabolism
  • Cognitive Dysfunction* / metabolism
  • Diet, Ketogenic*
  • Disease Models, Animal
  • Ferroptosis*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • NF-E2-Related Factor 2 / metabolism
  • Presenilin-1 / genetics
  • Presenilin-1 / metabolism

Substances

  • NF-E2-Related Factor 2
  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Presenilin-1