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

Authors :
Mardare, Cornelia
Krüger, Karsten
Liebisch, Gerhard
Seimetz, Michael
Couturier, Aline
Ringseis, Robert
Wilhelm, Jochen
Weissmann, Norbert
Eder, Klaus
Mooren, Frank-Christoph
Department of Sports Medicine
Source :
Journal of Diabetes Research, Vol 2016 (2016), Journal of Diabetes Research, Journal of Diabetes Research 2016:Article ID 4536470 doi:10.1155/2016/4536470
Publication Year :
2016
Publisher :
Hindawi Limited, 2016.

Abstract

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-alpha and IL-18 expression. Furthermore, ET reduced levels of MIP-1gamma, while RT decreased levels of IL-18, MIP-1gamma, 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.

Details

Language :
English
ISSN :
23146753 and 23146745
Volume :
2016
Database :
OpenAIRE
Journal :
Journal of Diabetes Research
Accession number :
edsair.pmid.dedup....4893b807c0842b3445c2282929923226