A modified Mediterranean-style diet enhances brain function via specific gut-microbiome-brain mechanisms

Gut Microbes. 2024 Jan-Dec;16(1):2323752. doi: 10.1080/19490976.2024.2323752. Epub 2024 Mar 6.

Abstract

Alzheimer's disease (AD) is a debilitating brain disorder with rapidly mounting prevalence worldwide, yet no proven AD cure has been discovered. Using a multi-omics approach in a transgenic AD mouse model, the current study demonstrated the efficacy of a modified Mediterranean-ketogenic diet (MkD) on AD-related neurocognitive pathophysiology and underlying mechanisms related to the gut-microbiome-brain axis. The findings revealed that MkD induces profound shifts in the gut microbiome community and microbial metabolites. Most notably, MkD promoted growth of the Lactobacillus population, resulting in increased bacteria-derived lactate production. We discovered elevated levels of microbiome- and diet-derived metabolites in the serum as well, signaling their influence on the brain. Importantly, these changes in serum metabolites upregulated specific receptors that have neuroprotective effects and induced alternations in neuroinflammatory-associated pathway profiles in hippocampus. Additionally, these metabolites displayed strong favorable co-regulation relationship with gut-brain integrity and inflammatory markers, as well as neurobehavioral outcomes. The findings underscore the ameliorative effects of MkD on AD-related neurological function and the underlying gut-brain communication via modulation of the gut microbiome-metabolome arrays.

Keywords: Alzheimer’s disease; Mediterranean diet; gut-brain axis; ketogenic diet; metabolome; microbiome; neurocognition; neurodegenerative disease; neuroinflammation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alzheimer Disease*
  • Animals
  • Brain
  • Brain-Gut Axis
  • Diet, Mediterranean*
  • Gastrointestinal Microbiome*
  • Mice
  • Microbiota*

Grants and funding

The study was supported by the Florida State University Council on Research & Creativity (FSU-CRC) funding program and the FSU College of Health & Human Sciences new investigator funding to RN. RN also acknowledges funding from the Infectious Diseases Society of America (IDSA), the United States Department of Agriculture (USDA-ARS #440658), and the Florida Department of Health (23A02 and 24A05). BW would like to thank the National Science Foundation (NSF; Grant No. 2245530) for support in metabolomics studies. The findings in this publication have not been formally disseminated by the funders and should not be construed to represent any agency determination or policy.