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No evidence of direct association between GLUT4 and glycogen in human skeletal muscle

Previous studies have demonstrated that exercise increases whole body and skeletal muscle insulin sensitivity that is linked with increased GLUT4 at the plasma membrane following insulin stimulation and associated with muscle glycogen depletion. To assess the potential direct association between mus...

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Autores principales: Murphy, Robyn M., Flores‐Opazo, Marcelo, Frankish, Barnaby P., Garnham, Andrew, Stapleton, David, Hargreaves, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429973/
https://www.ncbi.nlm.nih.gov/pubmed/30488593
http://dx.doi.org/10.14814/phy2.13917
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author Murphy, Robyn M.
Flores‐Opazo, Marcelo
Frankish, Barnaby P.
Garnham, Andrew
Stapleton, David
Hargreaves, Mark
author_facet Murphy, Robyn M.
Flores‐Opazo, Marcelo
Frankish, Barnaby P.
Garnham, Andrew
Stapleton, David
Hargreaves, Mark
author_sort Murphy, Robyn M.
collection PubMed
description Previous studies have demonstrated that exercise increases whole body and skeletal muscle insulin sensitivity that is linked with increased GLUT4 at the plasma membrane following insulin stimulation and associated with muscle glycogen depletion. To assess the potential direct association between muscle glycogen and GLUT4, seven untrained, male subjects exercised for 60 min at ~75% VO(2) peak, with muscle samples obtained by percutaneous needle biopsy immediately before and after exercise. Exercise reduced muscle glycogen content by ~43%. An ultracentrifugation protocol resulted in a ~2‐3‐fold enriched glycogen fraction from muscle samples for analysis. Total GLUT4 content was unaltered by exercise and we were unable to detect any GLUT4 in glycogen fractions, either with or without amylase treatment. In skinned muscle fiber segments, there was very little, if any, GLUT4 detected in wash solutions, except following exposure to 1% Triton X‐100. Amylase treatment of single fibers did not increase GLUT4 in the wash solution and there were no differences in GLUT4 content between fibers obtained before or after exercise for any of the wash treatments. Our results indicate no direct association between GLUT4 and glycogen in human skeletal muscle, before or after exercise, and suggest that alterations in GLUT4 translocation associated with exercise‐induced muscle glycogen depletion are mediated via other mechanisms.
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spelling pubmed-64299732019-04-15 No evidence of direct association between GLUT4 and glycogen in human skeletal muscle Murphy, Robyn M. Flores‐Opazo, Marcelo Frankish, Barnaby P. Garnham, Andrew Stapleton, David Hargreaves, Mark Physiol Rep Original Research Previous studies have demonstrated that exercise increases whole body and skeletal muscle insulin sensitivity that is linked with increased GLUT4 at the plasma membrane following insulin stimulation and associated with muscle glycogen depletion. To assess the potential direct association between muscle glycogen and GLUT4, seven untrained, male subjects exercised for 60 min at ~75% VO(2) peak, with muscle samples obtained by percutaneous needle biopsy immediately before and after exercise. Exercise reduced muscle glycogen content by ~43%. An ultracentrifugation protocol resulted in a ~2‐3‐fold enriched glycogen fraction from muscle samples for analysis. Total GLUT4 content was unaltered by exercise and we were unable to detect any GLUT4 in glycogen fractions, either with or without amylase treatment. In skinned muscle fiber segments, there was very little, if any, GLUT4 detected in wash solutions, except following exposure to 1% Triton X‐100. Amylase treatment of single fibers did not increase GLUT4 in the wash solution and there were no differences in GLUT4 content between fibers obtained before or after exercise for any of the wash treatments. Our results indicate no direct association between GLUT4 and glycogen in human skeletal muscle, before or after exercise, and suggest that alterations in GLUT4 translocation associated with exercise‐induced muscle glycogen depletion are mediated via other mechanisms. John Wiley and Sons Inc. 2018-11-22 /pmc/articles/PMC6429973/ /pubmed/30488593 http://dx.doi.org/10.14814/phy2.13917 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://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 Research
Murphy, Robyn M.
Flores‐Opazo, Marcelo
Frankish, Barnaby P.
Garnham, Andrew
Stapleton, David
Hargreaves, Mark
No evidence of direct association between GLUT4 and glycogen in human skeletal muscle
title No evidence of direct association between GLUT4 and glycogen in human skeletal muscle
title_full No evidence of direct association between GLUT4 and glycogen in human skeletal muscle
title_fullStr No evidence of direct association between GLUT4 and glycogen in human skeletal muscle
title_full_unstemmed No evidence of direct association between GLUT4 and glycogen in human skeletal muscle
title_short No evidence of direct association between GLUT4 and glycogen in human skeletal muscle
title_sort no evidence of direct association between glut4 and glycogen in human skeletal muscle
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429973/
https://www.ncbi.nlm.nih.gov/pubmed/30488593
http://dx.doi.org/10.14814/phy2.13917
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