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Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity
OBJECTIVE: To understand relationships between exercise training-mediated improvements in insulin sensitivity (S(I)) and changes in circulating concentrations of metabolic intermediates, hormones, and inflammatory mediators. RESEARCH DESIGN AND METHODS: Targeted mass spectrometry and enzyme-linked i...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005483/ https://www.ncbi.nlm.nih.gov/pubmed/20921216 http://dx.doi.org/10.2337/dc10-0709 |
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author | Huffman, Kim M. Slentz, Cris A. Bateman, Lori A. Thompson, Dana Muehlbauer, Michael J. Bain, James R. Stevens, Robert D. Wenner, Brett R. Kraus, Virginia Byers Newgard, Christopher B. Kraus, William E. |
author_facet | Huffman, Kim M. Slentz, Cris A. Bateman, Lori A. Thompson, Dana Muehlbauer, Michael J. Bain, James R. Stevens, Robert D. Wenner, Brett R. Kraus, Virginia Byers Newgard, Christopher B. Kraus, William E. |
author_sort | Huffman, Kim M. |
collection | PubMed |
description | OBJECTIVE: To understand relationships between exercise training-mediated improvements in insulin sensitivity (S(I)) and changes in circulating concentrations of metabolic intermediates, hormones, and inflammatory mediators. RESEARCH DESIGN AND METHODS: Targeted mass spectrometry and enzyme-linked immunosorbent assays were used to quantify metabolic intermediates, hormones, and inflammatory markers at baseline, after 6 months of exercise training, and 2 weeks after exercise training cessation (n = 53). A principal components analysis (PCA) strategy was used to relate changes in these intermediates to changes in S(I). RESULTS: PCA reduced the number of intermediates from 90 to 24 factors composed of biologically related components. With exercise training, improvements in S(I) were associated with reductions in by-products of fatty acid oxidation and increases in glycine and proline (P < 0.05, R(2) = 0.59); these relationships were retained 15 days after cessation of exercise training (P < 0.05, R(2) = 0.34). CONCLUSIONS: These observations support prior observations in animal models that exercise training promotes more efficient mitochondrial β-oxidation and challenges current hypotheses regarding exercise training and glycine metabolism. |
format | Text |
id | pubmed-3005483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-30054832012-01-01 Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity Huffman, Kim M. Slentz, Cris A. Bateman, Lori A. Thompson, Dana Muehlbauer, Michael J. Bain, James R. Stevens, Robert D. Wenner, Brett R. Kraus, Virginia Byers Newgard, Christopher B. Kraus, William E. Diabetes Care Original Research OBJECTIVE: To understand relationships between exercise training-mediated improvements in insulin sensitivity (S(I)) and changes in circulating concentrations of metabolic intermediates, hormones, and inflammatory mediators. RESEARCH DESIGN AND METHODS: Targeted mass spectrometry and enzyme-linked immunosorbent assays were used to quantify metabolic intermediates, hormones, and inflammatory markers at baseline, after 6 months of exercise training, and 2 weeks after exercise training cessation (n = 53). A principal components analysis (PCA) strategy was used to relate changes in these intermediates to changes in S(I). RESULTS: PCA reduced the number of intermediates from 90 to 24 factors composed of biologically related components. With exercise training, improvements in S(I) were associated with reductions in by-products of fatty acid oxidation and increases in glycine and proline (P < 0.05, R(2) = 0.59); these relationships were retained 15 days after cessation of exercise training (P < 0.05, R(2) = 0.34). CONCLUSIONS: These observations support prior observations in animal models that exercise training promotes more efficient mitochondrial β-oxidation and challenges current hypotheses regarding exercise training and glycine metabolism. American Diabetes Association 2011-01 2010-10-04 /pmc/articles/PMC3005483/ /pubmed/20921216 http://dx.doi.org/10.2337/dc10-0709 Text en © 2011 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 Huffman, Kim M. Slentz, Cris A. Bateman, Lori A. Thompson, Dana Muehlbauer, Michael J. Bain, James R. Stevens, Robert D. Wenner, Brett R. Kraus, Virginia Byers Newgard, Christopher B. Kraus, William E. Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity |
title | Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity |
title_full | Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity |
title_fullStr | Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity |
title_full_unstemmed | Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity |
title_short | Exercise-Induced Changes in Metabolic Intermediates, Hormones, and Inflammatory Markers Associated With Improvements in Insulin Sensitivity |
title_sort | exercise-induced changes in metabolic intermediates, hormones, and inflammatory markers associated with improvements in insulin sensitivity |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005483/ https://www.ncbi.nlm.nih.gov/pubmed/20921216 http://dx.doi.org/10.2337/dc10-0709 |
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