Dietary Methionine Restriction Alleviates Cognitive Impairment in Alzheimer's Disease Mice via Sex-Dependent Modulation on Gut Microbiota and Tryptophan Metabolism: A Multiomics Analysis

J Agric Food Chem. 2025 Jan 15;73(2):1356-1372. doi: 10.1021/acs.jafc.4c09878. Epub 2025 Jan 2.

Abstract

Plant-based foods with low methionine contents have gained increasing interest for their potential health benefits, including neuroprotective effects. Methionine restriction (MR) linked to a plant-based diet has been shown to mitigate neurodegenerative diseases such as Alzheimer's disease (AD) through mechanisms that involve the gut microbiota. In this study, a 16-week MR diet (0.17% methionine, w/w) improved working memory and reduced neuronal damage exclusively in 4-month-old male APP/PS1 AD mice. Transcriptomic analysis revealed the activation of serum- and glucose-corticoid-regulated kinase 1 (SGK1) and peroxisome proliferator-activated receptor α (PPARα) pathways. Furthermore, metabolomics demonstrated increased serum indole-3-propionic acid (IPA) levels and an enhanced expression of gut barrier proteins Claudin-1 and MUC2 in male mice. MR significantly altered the gut microbiota composition, notably increasing indole-producing bacteria such as Lactobacillus reuteri (L. reuteri). Multiomics integration linked L. reuteri, IPA, and PPARα signaling to improved cognitive outcomes. Molecular docking and RT-qPCR analyses confirmed IPA's interaction with PPARα, leading to the activation of neuroprotective targets (Bdnf, Pparα, Acsbg1, Scd2, and Scd3). These results highlight the role of methionine restriction in modulating gut microbiota and metabolites, offering a promising dietary approach to managing neurodegenerative diseases with sex-specific effects.

Keywords: Alzheimer’s disease; indole-3-propionic acid; methionine restriction; multiomics; peroxisome proliferator-activated receptor α; sexual dimorphism.

MeSH terms

  • Alzheimer Disease* / diet therapy
  • Alzheimer Disease* / metabolism
  • Animals
  • Bacteria / classification
  • Bacteria / genetics
  • Bacteria / isolation & purification
  • Bacteria / metabolism
  • Cognitive Dysfunction* / diet therapy
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / metabolism
  • Disease Models, Animal
  • Female
  • Gastrointestinal Microbiome*
  • Humans
  • Male
  • Methionine* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Multiomics
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • Tryptophan* / metabolism

Substances

  • Methionine
  • Tryptophan
  • PPAR alpha