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dc.rights.licenseopenen_US
hal.structure.identifierUniversity of Turku
dc.contributor.authorHAMED, Hany
dc.contributor.authorLEYROLLE, Quentin
hal.structure.identifierUniversity of Turku
hal.structure.identifierUniversity of Eastern Finland
dc.contributor.authorKOISTINEN, Ville
hal.structure.identifierUniversity of Eastern Finland
dc.contributor.authorKARKKAINEN, Olli
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorLAYE, Sophie
ORCID: 0000-0002-3843-1012
IDREF: 11366883X
dc.contributor.authorDELZENNE, Nathalie
hal.structure.identifierUniversity of Turku
hal.structure.identifierUniversity of Eastern Finland
dc.contributor.authorHANHINEVA, Kati
dc.date.accessioned2023-05-24T09:34:41Z
dc.date.available2023-05-24T09:34:41Z
dc.date.issued2022-07
dc.identifier.issn1949-0976en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182293
dc.description.abstractEnAlterations in the gut microbiota composition have been associated with a range of neurodevelopmental, neurodegenerative, and neuropsychiatric disorders. The gut microbes transform and metabolize dietary- and host-derived molecules generating a diverse group of metabolites with local and systemic effects. The bi-directional communication between brain and the microbes residing in the gut, the so-called gut–brain axis, consists of a network of immunological, neuronal, and endocrine signaling pathways. Although the full variety of mechanisms of the gut–brain crosstalk is yet to be established, the existing data demonstrates that a single metabolite or its derivatives are likely among the key inductors within the gut–brain axis communication. However, more research is needed to understand the molecular mechanisms underlying how gut microbiota associated metabolites alter brain functions, and to examine if different interventional approaches targeting the gut microbiota could be used in prevention and treatment of neurological disorders, as reviewed herein. Abbreviations:4-EPS 4-ethylphenylsulfate; 5-AVA(B) 5-aminovaleric acid (betaine); Aβ Amyloid beta protein; AhR Aryl hydrocarbon receptor; ASD Autism spectrum disorder; BBB Blood–brain barrier; BDNF Brain-derived neurotrophic factor; CNS Central nervous system; GABA ɣ-aminobutyric acid; GF Germ-free; MIA Maternal immune activation; SCFA Short-chain fatty acid; 3M-4-TMAB 3-methyl-4-(trimethylammonio)butanoate; 4-TMAP 4-(trimethylammonio)pentanoate; TMA(O) Trimethylamine(-N-oxide); TUDCA Tauroursodeoxycholic acid; ZO Zonula occludens proteins. © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enGut microbiota
dc.subject.enGut-brain axis
dc.subject.enMetabolism
dc.subject.enMetabolites
dc.subject.enshort-chain fatty acids
dc.title.enMicrobiota-derived metabolites as drivers of gut–brain communication
dc.typeArticle de revueen_US
dc.identifier.doi10.1080/19490976.2022.2102878en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed35903003en_US
bordeaux.journalGut microbesen_US
bordeaux.volume14en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDHorizon 2020en_US
hal.identifierhal-04104660
hal.version1
hal.date.transferred2023-05-24T09:34:51Z
hal.exporttrue
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Gut%20microbes&rft.date=2022-07&rft.volume=14&rft.issue=1&rft.eissn=1949-0976&rft.issn=1949-0976&rft.au=HAMED,%20Hany&LEYROLLE,%20Quentin&KOISTINEN,%20Ville&KARKKAINEN,%20Olli&LAYE,%20Sophie&rft.genre=article


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