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Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice

The study aimed to investigate the effects of differentiated exercise regimes on high fat-induced metabolic and inflammatory pathways. Mice were fed a standard diet (ST) or a high fat diet (HFD) and subjected to regular endurance training (ET) or resistance training (RT). After 10 weeks body weight,...

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Autores principales: Mardare, Cornelia, Krüger, Karsten, Liebisch, Gerhard, Seimetz, Michael, Couturier, Aline, Ringseis, Robert, Wilhelm, Jochen, Weissmann, Norbert, Eder, Klaus, Mooren, Frank-Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691630/
https://www.ncbi.nlm.nih.gov/pubmed/26788518
http://dx.doi.org/10.1155/2016/4536470
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author Mardare, Cornelia
Krüger, Karsten
Liebisch, Gerhard
Seimetz, Michael
Couturier, Aline
Ringseis, Robert
Wilhelm, Jochen
Weissmann, Norbert
Eder, Klaus
Mooren, Frank-Christoph
author_facet Mardare, Cornelia
Krüger, Karsten
Liebisch, Gerhard
Seimetz, Michael
Couturier, Aline
Ringseis, Robert
Wilhelm, Jochen
Weissmann, Norbert
Eder, Klaus
Mooren, Frank-Christoph
author_sort Mardare, Cornelia
collection PubMed
description The study aimed to investigate the effects of differentiated exercise regimes on high fat-induced metabolic and inflammatory pathways. Mice were fed a standard diet (ST) or a high fat diet (HFD) and subjected to regular endurance training (ET) or resistance training (RT). After 10 weeks body weight, glucose tolerance, fatty acids (FAs), circulating ceramides, cytokines, and immunological mediators were determined. The HFD induced a significant increase in body weight and a disturbed glucose tolerance (p < 0.05). An increase of plasma FA, ceramides, and inflammatory mediators in adipose tissue and serum was found (p < 0.05). Both endurance and resistance training decreased body weight (p < 0.05) and reduced serum ceramides (p < 0.005). While RT attenuated the increase of NLRP-3 (RT) expression in adipose tissue, ET was effective in reducing TNF-α and IL-18 expression. Furthermore, ET reduced levels of MIP-1γ, while RT decreased levels of IL-18, MIP-1γ, Timp-1, and CD40 in serum (p < 0.001), respectively. Although both exercise regimes improved glucose tolerance (p < 0.001), ET was more effective than RT. These results suggest that exercise improves HFD-induced complications possibly through a reduction of ceramides, the reduction of inflammasome activation in adipose tissues, and a systemic downregulation of inflammatory cytokines.
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spelling pubmed-46916302016-01-19 Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice Mardare, Cornelia Krüger, Karsten Liebisch, Gerhard Seimetz, Michael Couturier, Aline Ringseis, Robert Wilhelm, Jochen Weissmann, Norbert Eder, Klaus Mooren, Frank-Christoph J Diabetes Res Research Article The study aimed to investigate the effects of differentiated exercise regimes on high fat-induced metabolic and inflammatory pathways. Mice were fed a standard diet (ST) or a high fat diet (HFD) and subjected to regular endurance training (ET) or resistance training (RT). After 10 weeks body weight, glucose tolerance, fatty acids (FAs), circulating ceramides, cytokines, and immunological mediators were determined. The HFD induced a significant increase in body weight and a disturbed glucose tolerance (p < 0.05). An increase of plasma FA, ceramides, and inflammatory mediators in adipose tissue and serum was found (p < 0.05). Both endurance and resistance training decreased body weight (p < 0.05) and reduced serum ceramides (p < 0.005). While RT attenuated the increase of NLRP-3 (RT) expression in adipose tissue, ET was effective in reducing TNF-α and IL-18 expression. Furthermore, ET reduced levels of MIP-1γ, while RT decreased levels of IL-18, MIP-1γ, Timp-1, and CD40 in serum (p < 0.001), respectively. Although both exercise regimes improved glucose tolerance (p < 0.001), ET was more effective than RT. These results suggest that exercise improves HFD-induced complications possibly through a reduction of ceramides, the reduction of inflammasome activation in adipose tissues, and a systemic downregulation of inflammatory cytokines. Hindawi Publishing Corporation 2016 2015-12-14 /pmc/articles/PMC4691630/ /pubmed/26788518 http://dx.doi.org/10.1155/2016/4536470 Text en Copyright © 2016 Cornelia Mardare et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mardare, Cornelia
Krüger, Karsten
Liebisch, Gerhard
Seimetz, Michael
Couturier, Aline
Ringseis, Robert
Wilhelm, Jochen
Weissmann, Norbert
Eder, Klaus
Mooren, Frank-Christoph
Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice
title Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice
title_full Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice
title_fullStr Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice
title_full_unstemmed Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice
title_short Endurance and Resistance Training Affect High Fat Diet-Induced Increase of Ceramides, Inflammasome Expression, and Systemic Inflammation in Mice
title_sort endurance and resistance training affect high fat diet-induced increase of ceramides, inflammasome expression, and systemic inflammation in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691630/
https://www.ncbi.nlm.nih.gov/pubmed/26788518
http://dx.doi.org/10.1155/2016/4536470
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