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dc.rights.licenseopenen_US
dc.contributor.authorMETHEREL, Adam H.
dc.contributor.authorVALENZUELA, Rodrigo
dc.contributor.authorKLIEVIK, Brinley J.
dc.contributor.authorCISBANI, Giulia
dc.contributor.authorROTARESCU, Ruxandra D.
dc.contributor.authorGONZALEZ-SOTO, Melissa
dc.contributor.authorCRUCIANI-GUGLIELMACCI, Celine
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorLAYE, Sophie
dc.contributor.authorMAGNAN, Christophe
dc.contributor.authorMUTCH, David M.
dc.contributor.authorBAZINET, Richard P.
dc.date.accessioned2024-08-19T12:24:15Z
dc.date.available2024-08-19T12:24:15Z
dc.date.issued2024-06-01
dc.identifier.issn0022-2275en_US
dc.identifier.urioai:crossref.org:10.1016/j.jlr.2024.100548
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/201173
dc.description.abstractEnDHA is abundant in the brain where it regulates cell survival, neurogenesis, and neuroinflammation. DHA can be obtained from the diet or synthesized from alpha-linolenic acid (ALA; 18:3n-3) via a series of desaturation and elongation reactions occurring in the liver. Tracer studies suggest that dietary DHA can downregulate its own synthesis, but the mechanism remains undetermined and is the primary objective of this manuscript. First, we show by tracing 13C content (δ13C) of DHA via compound-specific isotope analysis, that following low dietary DHA, the brain receives DHA synthesized from ALA. We then show that dietary DHA increases mouse liver and serum EPA, which is dependant on ALA. Furthermore, by compound-specific isotope analysis we demonstrate that the source of increased EPA is slowed EPA metabolism, not increased DHA retroconversion as previously assumed. DHA feeding alone or with ALA lowered liver elongation of very long chain (ELOVL2, EPA elongation) enzyme activity despite no change in protein content. To further evaluate the role of ELOVL2, a liver-specific Elovl2 KO was generated showing that DHA feeding in the presence or absence of a functional liver ELOVL2 yields similar results. An enzyme competition assay for EPA elongation suggests both uncompetitive and noncompetitive inhibition by DHA depending on DHA levels. To translate our findings, we show that DHA supplementation in men and women increases EPA levels in a manner dependent on a SNP (rs953413) in the ELOVL2 gene. In conclusion, we identify a novel feedback inhibition pathway where dietary DHA downregulates its liver synthesis by inhibiting EPA elongation.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.sourcecrossref
dc.subject.enDietary fat
dc.subject.enKinetics
dc.subject.enLiver
dc.subject.enNutrition
dc.subject.enOmega-3 fatty acids
dc.subject.enEnzyme inhibition
dc.subject.enPolyunsaturated fatty acid
dc.subject.enFatty acid metabolism
dc.subject.enElongation of very long-chain
dc.title.enDietary docosahexaenoic acid (DHA) downregulates liver DHA synthesis by inhibiting eicosapentaenoic acid elongation
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.jlr.2024.100548en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed38649096en_US
bordeaux.journalJournal of Lipid Researchen_US
bordeaux.page100548en_US
bordeaux.volume65en_US
bordeaux.hal.laboratoriesNutriNeuro (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-04672746
hal.version1
hal.date.transferred2024-08-19T12:24:19Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcedissemin
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Lipid%20Research&rft.date=2024-06-01&rft.volume=65&rft.issue=6&rft.spage=100548&rft.epage=100548&rft.eissn=0022-2275&rft.issn=0022-2275&rft.au=METHEREL,%20Adam%20H.&VALENZUELA,%20Rodrigo&KLIEVIK,%20Brinley%20J.&CISBANI,%20Giulia&ROTARESCU,%20Ruxandra%20D.&rft.genre=article


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