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Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids
Metabolic sensing neurons in the ventromedial hypothalamus (VMH) alter their activity when ambient levels of metabolic substrates, such as glucose and fatty acids (FA), change. To assess the relationship between a high-fat diet (HFD; 60%) intake on feeding and serum and VMH FA levels, rats were trai...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964505/ https://www.ncbi.nlm.nih.gov/pubmed/24379353 http://dx.doi.org/10.2337/db13-1090 |
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author | Le Foll, Christelle Dunn-Meynell, Ambrose A. Miziorko, Henri M. Levin, Barry E. |
author_facet | Le Foll, Christelle Dunn-Meynell, Ambrose A. Miziorko, Henri M. Levin, Barry E. |
author_sort | Le Foll, Christelle |
collection | PubMed |
description | Metabolic sensing neurons in the ventromedial hypothalamus (VMH) alter their activity when ambient levels of metabolic substrates, such as glucose and fatty acids (FA), change. To assess the relationship between a high-fat diet (HFD; 60%) intake on feeding and serum and VMH FA levels, rats were trained to eat a low-fat diet (LFD; 13.5%) or an HFD in 3 h/day and were monitored with VMH FA microdialysis. Despite having higher serum levels, HFD rats had lower VMH FA levels but ate less from 3 to 6 h of refeeding than did LFD rats. However, VMH β-hydroxybutyrate (β-OHB) and VMH-to-serum β-OHB ratio levels were higher in HFD rats during the first 1 h of refeeding, suggesting that VMH astrocyte ketone production mediated their reduced intake. In fact, using calcium imaging in dissociated VMH neurons showed that ketone bodies overrode normal FA sensing, primarily by exciting neurons that were activated or inhibited by oleic acid. Importantly, bilateral inhibition of VMH ketone production with a 3-hydroxy-3-methylglutaryl-CoA synthase inhibitor reversed the 3- to 6-h HFD-induced inhibition of intake but had no effect in LFD-fed rats. These data suggest that a restricted HFD intake regimen inhibits caloric intake as a consequence of FA-induced VMH ketone body production by astrocytes. |
format | Online Article Text |
id | pubmed-3964505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-39645052015-04-01 Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids Le Foll, Christelle Dunn-Meynell, Ambrose A. Miziorko, Henri M. Levin, Barry E. Diabetes Metabolism Metabolic sensing neurons in the ventromedial hypothalamus (VMH) alter their activity when ambient levels of metabolic substrates, such as glucose and fatty acids (FA), change. To assess the relationship between a high-fat diet (HFD; 60%) intake on feeding and serum and VMH FA levels, rats were trained to eat a low-fat diet (LFD; 13.5%) or an HFD in 3 h/day and were monitored with VMH FA microdialysis. Despite having higher serum levels, HFD rats had lower VMH FA levels but ate less from 3 to 6 h of refeeding than did LFD rats. However, VMH β-hydroxybutyrate (β-OHB) and VMH-to-serum β-OHB ratio levels were higher in HFD rats during the first 1 h of refeeding, suggesting that VMH astrocyte ketone production mediated their reduced intake. In fact, using calcium imaging in dissociated VMH neurons showed that ketone bodies overrode normal FA sensing, primarily by exciting neurons that were activated or inhibited by oleic acid. Importantly, bilateral inhibition of VMH ketone production with a 3-hydroxy-3-methylglutaryl-CoA synthase inhibitor reversed the 3- to 6-h HFD-induced inhibition of intake but had no effect in LFD-fed rats. These data suggest that a restricted HFD intake regimen inhibits caloric intake as a consequence of FA-induced VMH ketone body production by astrocytes. American Diabetes Association 2014-04 2014-03-13 /pmc/articles/PMC3964505/ /pubmed/24379353 http://dx.doi.org/10.2337/db13-1090 Text en © 2014 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Metabolism Le Foll, Christelle Dunn-Meynell, Ambrose A. Miziorko, Henri M. Levin, Barry E. Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids |
title | Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids |
title_full | Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids |
title_fullStr | Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids |
title_full_unstemmed | Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids |
title_short | Regulation of Hypothalamic Neuronal Sensing and Food Intake by Ketone Bodies and Fatty Acids |
title_sort | regulation of hypothalamic neuronal sensing and food intake by ketone bodies and fatty acids |
topic | Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964505/ https://www.ncbi.nlm.nih.gov/pubmed/24379353 http://dx.doi.org/10.2337/db13-1090 |
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