| Literature DB >> 33027674 |
María Arnoriaga-Rodríguez1, Jordi Mayneris-Perxachs2, Aurelijus Burokas3, Oren Contreras-Rodríguez4, Gerard Blasco5, Clàudia Coll6, Carles Biarnés7, Romina Miranda-Olivos4, Jèssica Latorre2, José-Maria Moreno-Navarrete1, Anna Castells-Nobau2, Mònica Sabater2, María Encarnación Palomo-Buitrago8, Josep Puig9, Salvador Pedraza10, Jordi Gich11, Vicente Pérez-Brocal12, Wifredo Ricart1, Andrés Moya13, Xavier Fernández-Real14, Lluís Ramió-Torrentà15, Reinald Pamplona16, Joaquim Sol16, Mariona Jové16, Manuel Portero-Otin16, Rafael Maldonado17, José Manuel Fernández-Real18.
Abstract
The gut microbiome has been linked to fear extinction learning in animal models. Here, we aimed to explore the gut microbiome and memory domains according to obesity status. A specific microbiome profile associated with short-term memory, working memory, and the volume of the hippocampus and frontal regions of the brain differentially in human subjects with and without obesity. Plasma and fecal levels of aromatic amino acids, their catabolites, and vegetable-derived compounds were longitudinally associated with short-term and working memory. Functionally, microbiota transplantation from human subjects with obesity led to decreased memory scores in mice, aligning this trait from humans with that of recipient mice. RNA sequencing of the medial prefrontal cortex of mice revealed that short-term memory associated with aromatic amino acid pathways, inflammatory genes, and clusters of bacterial species. These results highlight the potential therapeutic value of targeting the gut microbiota for memory impairment, specifically in subjects with obesity.Entities:
Keywords: B vitamins; brain structure; cognition; memory; metabolomics; metagenomics; microbiome; obesity; one-carbon metabolism; tryptophan metabolites
Year: 2020 PMID: 33027674 DOI: 10.1016/j.cmet.2020.09.002
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287