Cargando…

Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice

High dietary fat intake induces significant whole‐body and skeletal muscle adaptations in mice, including increased capacity for fat oxidation and mitochondrial biogenesis. The impact of a diet that is high in fat and simple sugars (i.e., western diet [WD]), particularly on regulation of skeletal mu...

Descripción completa

Detalles Bibliográficos
Autores principales: McGowan, Erin M., Ehrlicher, Sarah E., Stierwalt, Harrison D., Robinson, Matthew M., Newsom, Sean A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768729/
https://www.ncbi.nlm.nih.gov/pubmed/36541261
http://dx.doi.org/10.14814/phy2.15543
_version_ 1784854234505674752
author McGowan, Erin M.
Ehrlicher, Sarah E.
Stierwalt, Harrison D.
Robinson, Matthew M.
Newsom, Sean A.
author_facet McGowan, Erin M.
Ehrlicher, Sarah E.
Stierwalt, Harrison D.
Robinson, Matthew M.
Newsom, Sean A.
author_sort McGowan, Erin M.
collection PubMed
description High dietary fat intake induces significant whole‐body and skeletal muscle adaptations in mice, including increased capacity for fat oxidation and mitochondrial biogenesis. The impact of a diet that is high in fat and simple sugars (i.e., western diet [WD]), particularly on regulation of skeletal muscle mitochondrial function, is less understood. The purpose of the current study was to determine physiologic adaptations in mitochondrial respiratory capacity in skeletal muscle during short‐term consumption of WD, including if adaptive responses to WD‐feeding are modified by concurrent exercise training or may be sex‐specific. Male and female C57BL/6J mice were randomized to consume low‐fat diet (LFD) or WD for 4 weeks, with some WD‐fed mice also performing concurrent treadmill training (WD + Ex). Group sizes were n = 4–7. Whole‐body metabolism was measured using in‐cage assessment of food intake and energy expenditure, DXA body composition analysis and insulin tolerance testing. High‐resolution respirometry of mitochondria isolated from quadriceps muscle was used to determine skeletal muscle mitochondrial respiratory function. Male mice fed WD gained mass (p < 0.001), due to increased fat mass (p < 0.001), and displayed greater respiratory capacity for both lipid and non‐lipid substrates compared with LFD mice (p < 0.05). There was no effect of concurrent treadmill training on maximal respiration (WD + Ex vs. WD). Female mice had non‐significant changes in body mass and composition as a function of the interventions, and no differences in skeletal muscle mitochondrial oxidative capacity. These findings indicate 4 weeks of WD feeding can increase skeletal muscle mitochondrial oxidative capacity among male mice; whereas WD, with or without exercise, had minimal impact on mass gain and skeletal muscle respiratory capacity among female mice. The translational relevance is that mitochondrial adaptation to increases in dietary fat intake that model WD may be related to differences in weight gain among male and female mice.
format Online
Article
Text
id pubmed-9768729
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-97687292022-12-23 Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice McGowan, Erin M. Ehrlicher, Sarah E. Stierwalt, Harrison D. Robinson, Matthew M. Newsom, Sean A. Physiol Rep Original Articles High dietary fat intake induces significant whole‐body and skeletal muscle adaptations in mice, including increased capacity for fat oxidation and mitochondrial biogenesis. The impact of a diet that is high in fat and simple sugars (i.e., western diet [WD]), particularly on regulation of skeletal muscle mitochondrial function, is less understood. The purpose of the current study was to determine physiologic adaptations in mitochondrial respiratory capacity in skeletal muscle during short‐term consumption of WD, including if adaptive responses to WD‐feeding are modified by concurrent exercise training or may be sex‐specific. Male and female C57BL/6J mice were randomized to consume low‐fat diet (LFD) or WD for 4 weeks, with some WD‐fed mice also performing concurrent treadmill training (WD + Ex). Group sizes were n = 4–7. Whole‐body metabolism was measured using in‐cage assessment of food intake and energy expenditure, DXA body composition analysis and insulin tolerance testing. High‐resolution respirometry of mitochondria isolated from quadriceps muscle was used to determine skeletal muscle mitochondrial respiratory function. Male mice fed WD gained mass (p < 0.001), due to increased fat mass (p < 0.001), and displayed greater respiratory capacity for both lipid and non‐lipid substrates compared with LFD mice (p < 0.05). There was no effect of concurrent treadmill training on maximal respiration (WD + Ex vs. WD). Female mice had non‐significant changes in body mass and composition as a function of the interventions, and no differences in skeletal muscle mitochondrial oxidative capacity. These findings indicate 4 weeks of WD feeding can increase skeletal muscle mitochondrial oxidative capacity among male mice; whereas WD, with or without exercise, had minimal impact on mass gain and skeletal muscle respiratory capacity among female mice. The translational relevance is that mitochondrial adaptation to increases in dietary fat intake that model WD may be related to differences in weight gain among male and female mice. John Wiley and Sons Inc. 2022-12-21 /pmc/articles/PMC9768729/ /pubmed/36541261 http://dx.doi.org/10.14814/phy2.15543 Text en © 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
McGowan, Erin M.
Ehrlicher, Sarah E.
Stierwalt, Harrison D.
Robinson, Matthew M.
Newsom, Sean A.
Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
title Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
title_full Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
title_fullStr Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
title_full_unstemmed Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
title_short Impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
title_sort impact of 4 weeks of western diet and aerobic exercise training on whole‐body phenotype and skeletal muscle mitochondrial respiration in male and female mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768729/
https://www.ncbi.nlm.nih.gov/pubmed/36541261
http://dx.doi.org/10.14814/phy2.15543
work_keys_str_mv AT mcgowanerinm impactof4weeksofwesterndietandaerobicexercisetrainingonwholebodyphenotypeandskeletalmusclemitochondrialrespirationinmaleandfemalemice
AT ehrlichersarahe impactof4weeksofwesterndietandaerobicexercisetrainingonwholebodyphenotypeandskeletalmusclemitochondrialrespirationinmaleandfemalemice
AT stierwaltharrisond impactof4weeksofwesterndietandaerobicexercisetrainingonwholebodyphenotypeandskeletalmusclemitochondrialrespirationinmaleandfemalemice
AT robinsonmatthewm impactof4weeksofwesterndietandaerobicexercisetrainingonwholebodyphenotypeandskeletalmusclemitochondrialrespirationinmaleandfemalemice
AT newsomseana impactof4weeksofwesterndietandaerobicexercisetrainingonwholebodyphenotypeandskeletalmusclemitochondrialrespirationinmaleandfemalemice