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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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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. |
format | Online Article Text |
id | pubmed-5344184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
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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