Cargando…

Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation

Ketone bodies have been shown to transiently stimulate food intake and modify energy homeostasis regulatory systems following cerebral infusion for a moderate period of time (<6 hours). As ketone bodies are usually enhanced during episodes of fasting, this effect might correspond to a physiologic...

Descripción completa

Detalles Bibliográficos
Autores principales: Carneiro, Lionel, Geller, Sarah, Hébert, Audrey, Repond, Cendrine, Fioramonti, Xavier, Leloup, Corinne, Pellerin, Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052612/
https://www.ncbi.nlm.nih.gov/pubmed/27708432
http://dx.doi.org/10.1038/srep34909
_version_ 1782458259648544768
author Carneiro, Lionel
Geller, Sarah
Hébert, Audrey
Repond, Cendrine
Fioramonti, Xavier
Leloup, Corinne
Pellerin, Luc
author_facet Carneiro, Lionel
Geller, Sarah
Hébert, Audrey
Repond, Cendrine
Fioramonti, Xavier
Leloup, Corinne
Pellerin, Luc
author_sort Carneiro, Lionel
collection PubMed
description Ketone bodies have been shown to transiently stimulate food intake and modify energy homeostasis regulatory systems following cerebral infusion for a moderate period of time (<6 hours). As ketone bodies are usually enhanced during episodes of fasting, this effect might correspond to a physiological regulation. In contrast, ketone bodies levels remain elevated for prolonged periods during obesity, and thus could play an important role in the development of this pathology. In order to understand this transition, ketone bodies were infused through a catheter inserted in the carotid to directly stimulate the brain for a period of 24 hours. Food ingested and blood circulating parameters involved in metabolic control as well as glucose homeostasis were determined. Results show that ketone bodies infusion for 24 hours increased food intake associated with a stimulation of hypothalamic orexigenic neuropeptides. Moreover, insulinemia was increased and caused a decrease in glucose production despite an increased resistance to insulin. The present study confirms that ketone bodies reaching the brain stimulates food intake. Moreover, we provide evidence that a prolonged hyperketonemia leads to a dysregulation of energy homeostasis control mechanisms. Finally, this study shows that brain exposure to ketone bodies alters insulin signaling and consequently glucose homeostasis.
format Online
Article
Text
id pubmed-5052612
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50526122016-10-19 Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation Carneiro, Lionel Geller, Sarah Hébert, Audrey Repond, Cendrine Fioramonti, Xavier Leloup, Corinne Pellerin, Luc Sci Rep Article Ketone bodies have been shown to transiently stimulate food intake and modify energy homeostasis regulatory systems following cerebral infusion for a moderate period of time (<6 hours). As ketone bodies are usually enhanced during episodes of fasting, this effect might correspond to a physiological regulation. In contrast, ketone bodies levels remain elevated for prolonged periods during obesity, and thus could play an important role in the development of this pathology. In order to understand this transition, ketone bodies were infused through a catheter inserted in the carotid to directly stimulate the brain for a period of 24 hours. Food ingested and blood circulating parameters involved in metabolic control as well as glucose homeostasis were determined. Results show that ketone bodies infusion for 24 hours increased food intake associated with a stimulation of hypothalamic orexigenic neuropeptides. Moreover, insulinemia was increased and caused a decrease in glucose production despite an increased resistance to insulin. The present study confirms that ketone bodies reaching the brain stimulates food intake. Moreover, we provide evidence that a prolonged hyperketonemia leads to a dysregulation of energy homeostasis control mechanisms. Finally, this study shows that brain exposure to ketone bodies alters insulin signaling and consequently glucose homeostasis. Nature Publishing Group 2016-10-06 /pmc/articles/PMC5052612/ /pubmed/27708432 http://dx.doi.org/10.1038/srep34909 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Carneiro, Lionel
Geller, Sarah
Hébert, Audrey
Repond, Cendrine
Fioramonti, Xavier
Leloup, Corinne
Pellerin, Luc
Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
title Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
title_full Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
title_fullStr Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
title_full_unstemmed Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
title_short Hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
title_sort hypothalamic sensing of ketone bodies after prolonged cerebral exposure leads to metabolic control dysregulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052612/
https://www.ncbi.nlm.nih.gov/pubmed/27708432
http://dx.doi.org/10.1038/srep34909
work_keys_str_mv AT carneirolionel hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation
AT gellersarah hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation
AT hebertaudrey hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation
AT repondcendrine hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation
AT fioramontixavier hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation
AT leloupcorinne hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation
AT pellerinluc hypothalamicsensingofketonebodiesafterprolongedcerebralexposureleadstometaboliccontroldysregulation