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Metabolic dysfunction following weight-cycling in male mice

BACKGROUND: Combatting over-weight or obesity can lead to large fluctuations in an individual’s body weight, often referred to as weight cycling or “yo-yo” dieting. Current evidence regarding the potentially damaging effects of these changes is conflicting. METHODS: Here, we assess the metabolic eff...

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Autores principales: Schofield, SE, Parkinson, JRC, Henley, AB, Sahuri, M, Sanchez-Canon, GJ, Bell, JD
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344184/
https://www.ncbi.nlm.nih.gov/pubmed/27840414
http://dx.doi.org/10.1038/ijo.2016.193
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author Schofield, SE
Parkinson, JRC
Henley, AB
Sahuri, M
Sanchez-Canon, GJ
Bell, JD
author_facet Schofield, SE
Parkinson, JRC
Henley, AB
Sahuri, M
Sanchez-Canon, GJ
Bell, JD
author_sort Schofield, SE
collection PubMed
description BACKGROUND: Combatting over-weight or obesity can lead to large fluctuations in an individual’s body weight, often referred to as weight cycling or “yo-yo” dieting. Current evidence regarding the potentially damaging effects of these changes is conflicting. METHODS: Here, we assess the metabolic effects of weight cycling in a murine model, comprising three dietary switches to normal or high fat diets at 6 week intervals; male C57BL/6 mice were fed either a control (C) or high fat (F) diet for 6 weeks (n=140/group). C and F groups were then either maintained on their initial diet (CC and FF respectively) or switched to a high fat (CF) or control (FC) diet (n=35/group). For the final 6 week interval, CC and CF groups were returned to the control diet (CCC and CFC groups) while FC and FF groups were placed on a high fat diet (FCF and FFF) (n=28/group). RESULTS: For the majority of metabolic outcomes changes aligned with dietary switches; however assessment of neuropeptides and receptors involved in appetite regulation and reward signalling pathways reveal variable patterns of expression. Furthermore, we demonstrate that multiple cycling events leads to a significant increase in internal fat deposition, even when compared to animals maintained on a high fat diet (Internal Fat: FCF: 7.4 ± 0.2g vs. FFF: 5.6 ± 0.2g; p<0.01). CONCLUSIONS: Increased internal adipose tissue is strongly linked to the development of metabolic syndrome associated conditions such as type 2 diabetes, cardiovascular disease and hypertension. While further work will be required to elucidate the mechanisms underlying the neuronal control of energy homeostasis, these studies provide a causative link between weight cycling and adverse health.
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spelling pubmed-53441842017-05-14 Metabolic dysfunction following weight-cycling in male mice Schofield, SE Parkinson, JRC Henley, AB Sahuri, M Sanchez-Canon, GJ Bell, JD Int J Obes (Lond) Article BACKGROUND: Combatting over-weight or obesity can lead to large fluctuations in an individual’s body weight, often referred to as weight cycling or “yo-yo” dieting. Current evidence regarding the potentially damaging effects of these changes is conflicting. METHODS: Here, we assess the metabolic effects of weight cycling in a murine model, comprising three dietary switches to normal or high fat diets at 6 week intervals; male C57BL/6 mice were fed either a control (C) or high fat (F) diet for 6 weeks (n=140/group). C and F groups were then either maintained on their initial diet (CC and FF respectively) or switched to a high fat (CF) or control (FC) diet (n=35/group). For the final 6 week interval, CC and CF groups were returned to the control diet (CCC and CFC groups) while FC and FF groups were placed on a high fat diet (FCF and FFF) (n=28/group). RESULTS: For the majority of metabolic outcomes changes aligned with dietary switches; however assessment of neuropeptides and receptors involved in appetite regulation and reward signalling pathways reveal variable patterns of expression. Furthermore, we demonstrate that multiple cycling events leads to a significant increase in internal fat deposition, even when compared to animals maintained on a high fat diet (Internal Fat: FCF: 7.4 ± 0.2g vs. FFF: 5.6 ± 0.2g; p<0.01). CONCLUSIONS: Increased internal adipose tissue is strongly linked to the development of metabolic syndrome associated conditions such as type 2 diabetes, cardiovascular disease and hypertension. While further work will be required to elucidate the mechanisms underlying the neuronal control of energy homeostasis, these studies provide a causative link between weight cycling and adverse health. 2016-11-14 2017-03 /pmc/articles/PMC5344184/ /pubmed/27840414 http://dx.doi.org/10.1038/ijo.2016.193 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Schofield, SE
Parkinson, JRC
Henley, AB
Sahuri, M
Sanchez-Canon, GJ
Bell, JD
Metabolic dysfunction following weight-cycling in male mice
title Metabolic dysfunction following weight-cycling in male mice
title_full Metabolic dysfunction following weight-cycling in male mice
title_fullStr Metabolic dysfunction following weight-cycling in male mice
title_full_unstemmed Metabolic dysfunction following weight-cycling in male mice
title_short Metabolic dysfunction following weight-cycling in male mice
title_sort metabolic dysfunction following weight-cycling in male mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344184/
https://www.ncbi.nlm.nih.gov/pubmed/27840414
http://dx.doi.org/10.1038/ijo.2016.193
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