Evidence for hypothalamic ketone body sensing: impact on food intake and peripheral metabolic responses in mice.

Détails

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Etat: Public
Version: Author's accepted manuscript
ID Serval
serval:BIB_43AB02AFD1D6
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Evidence for hypothalamic ketone body sensing: impact on food intake and peripheral metabolic responses in mice.
Périodique
American Journal of Physiology. Endocrinology and Metabolism
Auteur⸱e⸱s
Carneiro L., Geller S., Fioramonti X., Hébert A., Repond C., Leloup C., Pellerin L.
ISSN
1522-1555 (Electronic)
ISSN-L
0193-1849
Statut éditorial
Publié
Date de publication
2016
Peer-reviewed
Oui
Volume
310
Numéro
2
Pages
E103-E115
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Monocarboxylates have been implicated in the control of energy homeostasis. Among them, the putative role of ketone bodies produced notably during high-fat diet (HFD) has not been thoroughly explored. In this study, we aimed to determine the impact of a specific rise in cerebral ketone bodies on food intake and energy homeostasis regulation. A carotid infusion of ketone bodies was performed on mice to stimulate sensitive brain areas for 6 or 12 h. At each time point, food intake and different markers of energy homeostasis were analyzed to reveal the consequences of cerebral increase in ketone body level detection. First, an increase in food intake appeared over a 12-h period of brain ketone body perfusion. This stimulated food intake was associated with an increased expression of the hypothalamic neuropeptides NPY and AgRP as well as phosphorylated AMPK and is due to ketone bodies sensed by the brain, as blood ketone body levels did not change at that time. In parallel, gluconeogenesis and insulin sensitivity were transiently altered. Indeed, a dysregulation of glucose production and insulin secretion was observed after 6 h of ketone body perfusion, which reversed to normal at 12 h of perfusion. Altogether, these results suggest that an increase in brain ketone body concentration leads to hyperphagia and a transient perturbation of peripheral metabolic homeostasis.
Mots-clé
Adenylate Kinase/metabolism, Agouti-Related Protein/metabolism, Animals, Blood Glucose, Diet, High-Fat, Eating/drug effects, Eating/physiology, Energy Metabolism/drug effects, Energy Metabolism/physiology, Gluconeogenesis/drug effects, Gluconeogenesis/physiology, Homeostasis, Hypothalamus/drug effects, Hypothalamus/metabolism, Insulin Resistance/physiology, Ketone Bodies/pharmacology, Male, Mice, Mice, Inbred C57BL, Neuropeptide Y/metabolism, Phosphorylation/drug effects
Pubmed
Web of science
Création de la notice
09/11/2015 10:55
Dernière modification de la notice
20/08/2019 14:47
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