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dc.rights.licenseopenen_US
dc.contributor.authorCARNEIRO, Lionel
dc.contributor.authorFENECH, Claire
dc.contributor.authorLIENARD, Fabienne
dc.contributor.authorGRALL, Sylvie
dc.contributor.authorABED, Besma
dc.contributor.authorHAYDAR, Joulia
hal.structure.identifierNeurocentre Magendie : Physiopathologie de la Plasticité Neuronale [U1215 Inserm - UB]
dc.contributor.authorALLARD, Camille
dc.contributor.authorDESMOULINS, Lucie
dc.contributor.authorPACCOUD, Romain
dc.contributor.authorBRINDISI, Marie-Claude
dc.contributor.authorMOUILLOT, Thomas
dc.contributor.authorBRONDEL, Laurent
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorFIORAMONTI, Xavier
dc.contributor.authorPENICAUD, Luc
dc.contributor.authorJACQUIN-PIQUES, Agnès
dc.contributor.authorLELOUP, Corinne
dc.date.accessioned2025-03-31T08:34:25Z
dc.date.available2025-03-31T08:34:25Z
dc.date.issued2024
dc.identifier.issn1523-0864en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/205802
dc.description.abstractEnAims: Part of hypothalamic (mediobasal hypothalamus [MBH]) neurons detect changes in blood glucose levels that in turn coordinate the vagal control of insulin secretion. This control cascade requires the production of mitochondrial reactive oxygen species (mROS), which is altered in models of obesity and insulin resistance. Obese, insulin-resistant Zücker rats are characterized by hypothalamic hypersensitivity to glucose. This initiates an abnormal vagus-induced insulin secretion, associated with an overproduction of mROS in response to a low glucose dose. Here, we hypothesized that ghrelin, known to buffer reactive oxygen species (ROS) via mitochondrial function, may be a major component of the hypothalamic glucose hypersensitivity in the hypoghrelinemic obese Zücker rat. Results: Hypothalamic glucose hypersensitivity-induced insulin secretion of Zücker obese rats was reversed by ghrelin pretreatment. The overproduction of MBH mROS in response to a low glucose load no longer occurred in obese rats that had previously received the cerebral ghrelin infusion. This decrease in mROS production was accompanied by a normalization of oxidative phosphorylation (OXPHOS). Conversely, blocking the action of ghrelin with a growth hormone secretagogue receptor antagonist in a model of hyperghrelinemia (fasted rats) completely restored hypothalamic glucose sensing-induced insulin secretion that was almost absent in this physiological situation. Accordingly, ROS signaling and mitochondrial activity were increased by the ghrelin receptor antagonist. Innovation: These results demonstrate for the first time that ghrelin addressed only to the brain could have a protective effect on the defective control of insulin secretion in the insulin-resistant, hypoghrelinemic obese subject. Conclusions: Ghrelin, through its action on OXPHOS, modulates mROS signaling in response to cerebral hyperglycemia and the consequent vagal control of insulin secretion. In insulin-resistant obese states, brain hypoghrelinemia could be responsible for the nervous defect in insulin secretion.
dc.description.sponsorshipEffets des édulcorants sur la fonction vasculaire : identification du rôle de la famille des récepteurs du goût sucré T1R - ANR-19-CE21-0003en_US
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enBrain glucose sensing
dc.subject.enGhrelin
dc.subject.enObesity
dc.subject.enInsulin resistance
dc.subject.enMitochondria
dc.subject.enROS
dc.title.enHypothalamic Glucose Hypersensitivity-Induced Insulin Secretion in the Obese Zücker Rat Is Reversed by Central Ghrelin Treatment
dc.typeArticle de revueen_US
dc.identifier.doi10.1089/ars.2022.0031en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed36656675en_US
bordeaux.journalAntioxidants and Redox Signalingen_US
bordeaux.page837 – 849en_US
bordeaux.volume40en_US
bordeaux.hal.laboratoriesNutriNeuro (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue13-15en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.institutionINSERM
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Antioxidants%20and%20Redox%20Signaling&rft.date=2024&rft.volume=40&rft.issue=13-15&rft.spage=837%20%E2%80%93%20849&rft.epage=837%20%E2%80%93%20849&rft.eissn=1523-0864&rft.issn=1523-0864&rft.au=CARNEIRO,%20Lionel&FENECH,%20Claire&LIENARD,%20Fabienne&GRALL,%20Sylvie&ABED,%20Besma&rft.genre=article


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