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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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 |
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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 |
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