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Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice

Muscle lipid increases with high-fat feeding and diabetes. In trained athletes, increased muscle lipid is not associated with insulin resistance, a phenomenon known as the athlete’s paradox. To understand if exercise altered the phenotype of muscle lipid, female C57BL/6 mice fed CTL or high-fat diet...

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Autores principales: Morton, Tiffany L., Galior, Kornelia, McGrath, Cody, Wu, Xin, Uzer, Gunes, Uzer, Guniz Bas, Sen, Buer, Xie, Zhihui, Tyson, David, Rubin, Janet, Styner, Maya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928595/
https://www.ncbi.nlm.nih.gov/pubmed/27445983
http://dx.doi.org/10.3389/fendo.2016.00080
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author Morton, Tiffany L.
Galior, Kornelia
McGrath, Cody
Wu, Xin
Uzer, Gunes
Uzer, Guniz Bas
Sen, Buer
Xie, Zhihui
Tyson, David
Rubin, Janet
Styner, Maya
author_facet Morton, Tiffany L.
Galior, Kornelia
McGrath, Cody
Wu, Xin
Uzer, Gunes
Uzer, Guniz Bas
Sen, Buer
Xie, Zhihui
Tyson, David
Rubin, Janet
Styner, Maya
author_sort Morton, Tiffany L.
collection PubMed
description Muscle lipid increases with high-fat feeding and diabetes. In trained athletes, increased muscle lipid is not associated with insulin resistance, a phenomenon known as the athlete’s paradox. To understand if exercise altered the phenotype of muscle lipid, female C57BL/6 mice fed CTL or high-fat diet (HFD for 6 or 18 weeks) were further divided into sedentary or exercising groups (CTL-E or HFD-E) with voluntary access to running wheels for the last 6 weeks of experiments, running 6 h/night. Diet did not affect running time or distance. HFD mice weighed more than CTL after 18 weeks (p < 0.01). Quadriceps muscle TG was increased in running animals and in sedentary mice fed HFD for 18 weeks (p < 0.05). In exercised animals, markers of fat, Plin1, aP2, FSP27, and Fasn, were increased significantly in HFD groups. Ucp1 and Pgc1a, markers for brown fat, increased with exercise in the setting of high fat feeding. Fndc5, which encodes irisin, and CytC were sensitive to exercise regardless of diet. Plin5 was increased with HFD and unaffected by exercise; the respiratory exchange ratio was 15% lower in the 18-week HFD group compared with CTL (p < 0.001) and 10% lower in 18 weeks HFD-E compared with CTL-E (p < 0.001). Increased Ucp1 and Pgc1a in exercised muscle of running mice suggests that a beige/brown fat phenotype develops, which differs from the fat phenotype that induces insulin resistance in high fat feeding. This suggests that increased muscle lipid may develop a “brown” phenotype in the setting of endurance exercise training, a shift that is further promoted by HFD.
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spelling pubmed-49285952016-07-21 Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice Morton, Tiffany L. Galior, Kornelia McGrath, Cody Wu, Xin Uzer, Gunes Uzer, Guniz Bas Sen, Buer Xie, Zhihui Tyson, David Rubin, Janet Styner, Maya Front Endocrinol (Lausanne) Endocrinology Muscle lipid increases with high-fat feeding and diabetes. In trained athletes, increased muscle lipid is not associated with insulin resistance, a phenomenon known as the athlete’s paradox. To understand if exercise altered the phenotype of muscle lipid, female C57BL/6 mice fed CTL or high-fat diet (HFD for 6 or 18 weeks) were further divided into sedentary or exercising groups (CTL-E or HFD-E) with voluntary access to running wheels for the last 6 weeks of experiments, running 6 h/night. Diet did not affect running time or distance. HFD mice weighed more than CTL after 18 weeks (p < 0.01). Quadriceps muscle TG was increased in running animals and in sedentary mice fed HFD for 18 weeks (p < 0.05). In exercised animals, markers of fat, Plin1, aP2, FSP27, and Fasn, were increased significantly in HFD groups. Ucp1 and Pgc1a, markers for brown fat, increased with exercise in the setting of high fat feeding. Fndc5, which encodes irisin, and CytC were sensitive to exercise regardless of diet. Plin5 was increased with HFD and unaffected by exercise; the respiratory exchange ratio was 15% lower in the 18-week HFD group compared with CTL (p < 0.001) and 10% lower in 18 weeks HFD-E compared with CTL-E (p < 0.001). Increased Ucp1 and Pgc1a in exercised muscle of running mice suggests that a beige/brown fat phenotype develops, which differs from the fat phenotype that induces insulin resistance in high fat feeding. This suggests that increased muscle lipid may develop a “brown” phenotype in the setting of endurance exercise training, a shift that is further promoted by HFD. Frontiers Media S.A. 2016-06-30 /pmc/articles/PMC4928595/ /pubmed/27445983 http://dx.doi.org/10.3389/fendo.2016.00080 Text en Copyright © 2016 Morton, Galior, McGrath, Wu, Uzer, Uzer, Sen, Xie, Tyson, Rubin and Styner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Morton, Tiffany L.
Galior, Kornelia
McGrath, Cody
Wu, Xin
Uzer, Gunes
Uzer, Guniz Bas
Sen, Buer
Xie, Zhihui
Tyson, David
Rubin, Janet
Styner, Maya
Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice
title Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice
title_full Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice
title_fullStr Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice
title_full_unstemmed Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice
title_short Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice
title_sort exercise increases and browns muscle lipid in high-fat diet-fed mice
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928595/
https://www.ncbi.nlm.nih.gov/pubmed/27445983
http://dx.doi.org/10.3389/fendo.2016.00080
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