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Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men
Obesity, sedentary lifestyle and aging are associated with mitochondrial dysfunction and impaired insulin sensitivity. Acute exercise increases insulin sensitivity in skeletal muscle; however, whether mitochondria are involved in these processes remains unclear. The aim of this study was to investig...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697830/ https://www.ncbi.nlm.nih.gov/pubmed/29161316 http://dx.doi.org/10.1371/journal.pone.0188421 |
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author | Trewin, Adam J. Levinger, Itamar Parker, Lewan Shaw, Christopher S. Serpiello, Fabio R. Anderson, Mitchell J. McConell, Glenn K. Hare, David L. Stepto, Nigel K. |
author_facet | Trewin, Adam J. Levinger, Itamar Parker, Lewan Shaw, Christopher S. Serpiello, Fabio R. Anderson, Mitchell J. McConell, Glenn K. Hare, David L. Stepto, Nigel K. |
author_sort | Trewin, Adam J. |
collection | PubMed |
description | Obesity, sedentary lifestyle and aging are associated with mitochondrial dysfunction and impaired insulin sensitivity. Acute exercise increases insulin sensitivity in skeletal muscle; however, whether mitochondria are involved in these processes remains unclear. The aim of this study was to investigate the effects of insulin stimulation at rest and after acute exercise on skeletal muscle mitochondrial respiratory function (JO(2)) and hydrogen peroxide emission (JH(2)O(2)), and the associations with insulin sensitivity in obese, sedentary men. Nine men (means ± SD: 57 ± 6 years; BMI 33 ± 5 kg.m(2)) underwent hyperinsulinemic-euglycemic clamps in two separate trials 1–3 weeks apart: one under resting conditions, and another 1 hour after high-intensity exercise (4x4 min cycling at 95% HR(peak)). Muscle biopsies were obtained at baseline, and pre/post clamp to measure JO(2) with high-resolution respirometry and JH(2)O(2) via Amplex UltraRed from permeabilized fibers. Post-exercise, both JO(2) and JH(2)O(2) during ADP stimulated state-3/OXPHOS respiration were lower compared to baseline (P<0.05), but not after subsequent insulin stimulation. JH(2)O(2) was lower post-exercise and after subsequent insulin stimulation compared to insulin stimulation in the rest trial during succinate supported state-4/leak respiration (P<0.05). In contrast, JH(2)O(2) increased during complex-I supported leak respiration with insulin after exercise compared with resting conditions (P<0.05). Resting insulin sensitivity and JH(2)O(2) during complex-I leak respiration were positively correlated (r = 0.77, P<0.05). We conclude that in obese, older and sedentary men, acute exercise modifies skeletal muscle mitochondrial respiration and H(2)O(2) emission responses to hyperinsulinemia in a respiratory state-specific manner, which may have implications for metabolic diseases involving insulin resistance. |
format | Online Article Text |
id | pubmed-5697830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56978302017-11-30 Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men Trewin, Adam J. Levinger, Itamar Parker, Lewan Shaw, Christopher S. Serpiello, Fabio R. Anderson, Mitchell J. McConell, Glenn K. Hare, David L. Stepto, Nigel K. PLoS One Research Article Obesity, sedentary lifestyle and aging are associated with mitochondrial dysfunction and impaired insulin sensitivity. Acute exercise increases insulin sensitivity in skeletal muscle; however, whether mitochondria are involved in these processes remains unclear. The aim of this study was to investigate the effects of insulin stimulation at rest and after acute exercise on skeletal muscle mitochondrial respiratory function (JO(2)) and hydrogen peroxide emission (JH(2)O(2)), and the associations with insulin sensitivity in obese, sedentary men. Nine men (means ± SD: 57 ± 6 years; BMI 33 ± 5 kg.m(2)) underwent hyperinsulinemic-euglycemic clamps in two separate trials 1–3 weeks apart: one under resting conditions, and another 1 hour after high-intensity exercise (4x4 min cycling at 95% HR(peak)). Muscle biopsies were obtained at baseline, and pre/post clamp to measure JO(2) with high-resolution respirometry and JH(2)O(2) via Amplex UltraRed from permeabilized fibers. Post-exercise, both JO(2) and JH(2)O(2) during ADP stimulated state-3/OXPHOS respiration were lower compared to baseline (P<0.05), but not after subsequent insulin stimulation. JH(2)O(2) was lower post-exercise and after subsequent insulin stimulation compared to insulin stimulation in the rest trial during succinate supported state-4/leak respiration (P<0.05). In contrast, JH(2)O(2) increased during complex-I supported leak respiration with insulin after exercise compared with resting conditions (P<0.05). Resting insulin sensitivity and JH(2)O(2) during complex-I leak respiration were positively correlated (r = 0.77, P<0.05). We conclude that in obese, older and sedentary men, acute exercise modifies skeletal muscle mitochondrial respiration and H(2)O(2) emission responses to hyperinsulinemia in a respiratory state-specific manner, which may have implications for metabolic diseases involving insulin resistance. Public Library of Science 2017-11-21 /pmc/articles/PMC5697830/ /pubmed/29161316 http://dx.doi.org/10.1371/journal.pone.0188421 Text en © 2017 Trewin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Trewin, Adam J. Levinger, Itamar Parker, Lewan Shaw, Christopher S. Serpiello, Fabio R. Anderson, Mitchell J. McConell, Glenn K. Hare, David L. Stepto, Nigel K. Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
title | Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
title_full | Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
title_fullStr | Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
title_full_unstemmed | Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
title_short | Acute exercise alters skeletal muscle mitochondrial respiration and H(2)O(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
title_sort | acute exercise alters skeletal muscle mitochondrial respiration and h(2)o(2) emission in response to hyperinsulinemic-euglycemic clamp in middle-aged obese men |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697830/ https://www.ncbi.nlm.nih.gov/pubmed/29161316 http://dx.doi.org/10.1371/journal.pone.0188421 |
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