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dc.rights.licenseopenen_US
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorDUCROCQ, Fabien
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorWALLE, Roman
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorCONTINI, Andrea
dc.contributor.authorMASSON, Elodie A.Y.
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorOUMMADI, Asma
dc.contributor.authorBARREDA, G.
dc.contributor.authorMA, D.
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorBOSCH BOUJU, Clementine
ORCID: 0000-0001-8869-768X
IDREF: 156530244
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorDE SMEDT-PEYRUSSE, Veronique
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorTRIFILIEFF, Pierre
dc.date.accessioned2021-09-20T12:43:52Z
dc.date.available2021-09-20T12:43:52Z
dc.date.issued2019-04
dc.date.conference2019-04-28
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/112247
dc.descriptionPosteren_US
dc.description.abstractEnVarious, though distinct psychiatric disorders, such as Schizophrenia, bipolar disorder or major depression are associated with a dysfunction of the reward system linked to an alteration of dopamine transmission. Furthermore, these pathologies are also accompanied by changes in lipid metabolism and in particular a decrease in the brain content n-3 polyunsaturated fatty acid (PUFA) in the nervous system. However, the implication of brain lipid composition in the etiology of psychiatric endophenotypes has been overlooked. The aim of this study was to investigate a potential causal link between n-3 PUFA deficiency and deficits in reward processing. Using operant conditioning tasks in mice, we showed that developmental n-3 PUFA deficiency leads to a selective motivational deficit at adulthood that is reversed by n-3 PUFA supplementation starting at birth. In parallel, we showed that n-3 PUFA deficiency leads to alterations in electrophysiological properties of medium spiny neurons (MSNs) in the nucleus accumbens, main actors for motivational processes. MSNs from the direct pathway (dMSNs) displayed a decrease in excitability paralleled with an increase of inhibitory input onto these neurons. Using pharmacogenetic and transgenic approaches, we showed that 1) alterations in dMSNs directly results from increased inhibitory input from MSNs of the indirect pathway (iMSNs), called lateral inhibition and 2) rescuing appropriate PUFA levels in D2R-expressing neurons selectively (including iMSNs), was sufficient to reverse both alterations in electrophysiological properties of dMSNs and motivational deficit observed in n-3 PUFA deficient mice.
dc.language.isoENen_US
dc.title.enVulnerability of the nucleus accumbens neuronal network to developmental n-3 PUFA deficiency: consequences on the reward and motivation system
dc.typeAutre communication scientifique (congrès sans actes - poster - séminaire...)en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.conference.titleIBAGS Meetingen_US
bordeaux.countryfren_US
bordeaux.teamPsychoneuroimmunologie et Nutrition: Approches expérimentales et cliniquesen_US
bordeaux.teamNutrition, mémoire et glucocorticoïdesen_US
bordeaux.conference.cityBiarritzen_US
bordeaux.peerReviewedouien_US
hal.exportfalse
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.date=2019-04&rft.au=DUCROCQ,%20Fabien&WALLE,%20Roman&CONTINI,%20Andrea&MASSON,%20Elodie%20A.Y.&OUMMADI,%20Asma&rft.genre=conference


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