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Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men
BACKGROUND/OBJECTIVES: Animal studies and pilot experiments in men indicate that the hypothalamic neuropeptide oxytocin limits food intake, and raise the question of its potential to improve metabolic control in obesity. SUBJECTS/METHODS: We compared the effect of central nervous oxytocin administra...
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/PMC5116063/ https://www.ncbi.nlm.nih.gov/pubmed/27553712 http://dx.doi.org/10.1038/ijo.2016.149 |
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author | Thienel, M Fritsche, A Heinrichs, M Peter, A Ewers, M Lehnert, H Born, J Hallschmid, M |
author_facet | Thienel, M Fritsche, A Heinrichs, M Peter, A Ewers, M Lehnert, H Born, J Hallschmid, M |
author_sort | Thienel, M |
collection | PubMed |
description | BACKGROUND/OBJECTIVES: Animal studies and pilot experiments in men indicate that the hypothalamic neuropeptide oxytocin limits food intake, and raise the question of its potential to improve metabolic control in obesity. SUBJECTS/METHODS: We compared the effect of central nervous oxytocin administration (24 IU) via the intranasal route on ingestive behaviour and metabolic function in 18 young obese men with the results in a group of 20 normal-weight men. In double-blind, placebo-controlled experiments, ad libitum food intake from a test buffet was examined in fasted subjects 45 min after oxytocin administration, followed by the assessment of postprandial, reward-driven snack intake. Energy expenditure was repeatedly assessed by indirect calorimetry and blood was sampled to determine concentrations of blood glucose and hormones. RESULTS: Oxytocin markedly reduced hunger-driven food intake in the fasted state in obese but not in normal-weight men, and led to a reduction in snack consumption in both groups, whereas energy expenditure remained generally unaffected. Hypothalamic–pituitary–adrenal axis secretion and the postprandial rise in plasma glucose were blunted by oxytocin in both groups. CONCLUSIONS: Oxytocin exerts an acutely inhibitory impact on food intake that is enhanced rather than decreased in obese compared with normal-weight men. This pattern puts it in contrast to other metabolically active neuropeptides and bodes well for clinical applications of oxytocin in the treatment of metabolic disorders. |
format | Online Article Text |
id | pubmed-5116063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51160632016-12-06 Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men Thienel, M Fritsche, A Heinrichs, M Peter, A Ewers, M Lehnert, H Born, J Hallschmid, M Int J Obes (Lond) Original Article BACKGROUND/OBJECTIVES: Animal studies and pilot experiments in men indicate that the hypothalamic neuropeptide oxytocin limits food intake, and raise the question of its potential to improve metabolic control in obesity. SUBJECTS/METHODS: We compared the effect of central nervous oxytocin administration (24 IU) via the intranasal route on ingestive behaviour and metabolic function in 18 young obese men with the results in a group of 20 normal-weight men. In double-blind, placebo-controlled experiments, ad libitum food intake from a test buffet was examined in fasted subjects 45 min after oxytocin administration, followed by the assessment of postprandial, reward-driven snack intake. Energy expenditure was repeatedly assessed by indirect calorimetry and blood was sampled to determine concentrations of blood glucose and hormones. RESULTS: Oxytocin markedly reduced hunger-driven food intake in the fasted state in obese but not in normal-weight men, and led to a reduction in snack consumption in both groups, whereas energy expenditure remained generally unaffected. Hypothalamic–pituitary–adrenal axis secretion and the postprandial rise in plasma glucose were blunted by oxytocin in both groups. CONCLUSIONS: Oxytocin exerts an acutely inhibitory impact on food intake that is enhanced rather than decreased in obese compared with normal-weight men. This pattern puts it in contrast to other metabolically active neuropeptides and bodes well for clinical applications of oxytocin in the treatment of metabolic disorders. Nature Publishing Group 2016-11 2016-09-13 /pmc/articles/PMC5116063/ /pubmed/27553712 http://dx.doi.org/10.1038/ijo.2016.149 Text en Copyright © 2016 Macmillan Publishers Limited, part of Springer Nature. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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-nc-nd/4.0/ |
spellingShingle | Original Article Thienel, M Fritsche, A Heinrichs, M Peter, A Ewers, M Lehnert, H Born, J Hallschmid, M Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
title | Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
title_full | Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
title_fullStr | Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
title_full_unstemmed | Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
title_short | Oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
title_sort | oxytocin's inhibitory effect on food intake is stronger in obese than normal-weight men |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116063/ https://www.ncbi.nlm.nih.gov/pubmed/27553712 http://dx.doi.org/10.1038/ijo.2016.149 |
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