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Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training
The purpose of this study was to determine if site-specific phosphorylation at the level of Akt substrate of 160 kDa (AS160) is altered in skeletal muscle from sedentary humans across a wide range of the adult life span (18–84 years of age) and if endurance- and/or strength-oriented exercise trainin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781473/ https://www.ncbi.nlm.nih.gov/pubmed/23801578 http://dx.doi.org/10.2337/db13-0229 |
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author | Consitt, Leslie A. Van Meter, Jessica Newton, Christopher A. Collier, David N. Dar, Moahad S. Wojtaszewski, Jørgen F.P. Treebak, Jonas T. Tanner, Charles J. Houmard, Joseph A. |
author_facet | Consitt, Leslie A. Van Meter, Jessica Newton, Christopher A. Collier, David N. Dar, Moahad S. Wojtaszewski, Jørgen F.P. Treebak, Jonas T. Tanner, Charles J. Houmard, Joseph A. |
author_sort | Consitt, Leslie A. |
collection | PubMed |
description | The purpose of this study was to determine if site-specific phosphorylation at the level of Akt substrate of 160 kDa (AS160) is altered in skeletal muscle from sedentary humans across a wide range of the adult life span (18–84 years of age) and if endurance- and/or strength-oriented exercise training could rescue decrements in insulin action and skeletal muscle AS160 phosphorylation. A euglycemic-hyperinsulinemic clamp and skeletal muscle biopsies were performed in 73 individuals encompassing a wide age range (18–84 years of age), and insulin-stimulated AS160 phosphorylation was determined. Decrements in whole-body insulin action were associated with impairments in insulin-induced phosphorylation of skeletal muscle AS160 on sites Ser-588, Thr-642, Ser-666, and phospho-Akt substrate, but not Ser-318 or Ser-751. Twelve weeks of endurance- or strength-oriented exercise training increased whole-body insulin action and reversed impairments in AS160 phosphorylation evident in insulin-resistant aged individuals. These findings suggest that a dampening of insulin-induced phosphorylation of AS160 on specific sites in skeletal muscle contributes to the insulin resistance evident in a sedentary aging population and that exercise training is an effective intervention for treating these impairments. |
format | Online Article Text |
id | pubmed-3781473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-37814732014-10-01 Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training Consitt, Leslie A. Van Meter, Jessica Newton, Christopher A. Collier, David N. Dar, Moahad S. Wojtaszewski, Jørgen F.P. Treebak, Jonas T. Tanner, Charles J. Houmard, Joseph A. Diabetes Original Research The purpose of this study was to determine if site-specific phosphorylation at the level of Akt substrate of 160 kDa (AS160) is altered in skeletal muscle from sedentary humans across a wide range of the adult life span (18–84 years of age) and if endurance- and/or strength-oriented exercise training could rescue decrements in insulin action and skeletal muscle AS160 phosphorylation. A euglycemic-hyperinsulinemic clamp and skeletal muscle biopsies were performed in 73 individuals encompassing a wide age range (18–84 years of age), and insulin-stimulated AS160 phosphorylation was determined. Decrements in whole-body insulin action were associated with impairments in insulin-induced phosphorylation of skeletal muscle AS160 on sites Ser-588, Thr-642, Ser-666, and phospho-Akt substrate, but not Ser-318 or Ser-751. Twelve weeks of endurance- or strength-oriented exercise training increased whole-body insulin action and reversed impairments in AS160 phosphorylation evident in insulin-resistant aged individuals. These findings suggest that a dampening of insulin-induced phosphorylation of AS160 on specific sites in skeletal muscle contributes to the insulin resistance evident in a sedentary aging population and that exercise training is an effective intervention for treating these impairments. American Diabetes Association 2013-10 2013-09-17 /pmc/articles/PMC3781473/ /pubmed/23801578 http://dx.doi.org/10.2337/db13-0229 Text en © 2013 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Original Research Consitt, Leslie A. Van Meter, Jessica Newton, Christopher A. Collier, David N. Dar, Moahad S. Wojtaszewski, Jørgen F.P. Treebak, Jonas T. Tanner, Charles J. Houmard, Joseph A. Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training |
title | Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training |
title_full | Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training |
title_fullStr | Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training |
title_full_unstemmed | Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training |
title_short | Impairments in Site-Specific AS160 Phosphorylation and Effects of Exercise Training |
title_sort | impairments in site-specific as160 phosphorylation and effects of exercise training |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781473/ https://www.ncbi.nlm.nih.gov/pubmed/23801578 http://dx.doi.org/10.2337/db13-0229 |
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