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A procession of metabolic alterations accompanying muscle senescence in Manduca sexta
Biological aging profoundly impairs muscle function, performance, and metabolism. Because the progression of metabolic alterations associated with aging muscle has not been chronicled, we tracked the metabolic profiles of flight muscle from middle to advanced age in Manduca sexta to identify key mol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772441/ https://www.ncbi.nlm.nih.gov/pubmed/29343811 http://dx.doi.org/10.1038/s41598-018-19630-5 |
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author | Wone, Bernard W. M. Kinchen, Jason M. Kaup, Elana R. Wone, Beate |
author_facet | Wone, Bernard W. M. Kinchen, Jason M. Kaup, Elana R. Wone, Beate |
author_sort | Wone, Bernard W. M. |
collection | PubMed |
description | Biological aging profoundly impairs muscle function, performance, and metabolism. Because the progression of metabolic alterations associated with aging muscle has not been chronicled, we tracked the metabolic profiles of flight muscle from middle to advanced age in Manduca sexta to identify key molecules during the progression of muscle aging, as well as to evaluate the utility of the M. sexta system for molecular dissection of muscle aging. We identified a number of differences between Diel Time, Sexes, and Muscle Ages, including changes in metabolites related to energetics, extracellular matrix turnover, and glutathione metabolism. Increased abundances of glycolytic metabolites suggest a shift toward increased glycolysis with advancing age, whereas decreased abundances in lysolipids and acylcarnitines reflect decreasing beta-oxidation. We also observed a shift towards decreased polyamine metabolism with age, which might result in an age-related decline in lipid metabolism possibly due to regulation of energy metabolism by polyamines. Collectively, our findings demonstrate the feasibility of our system and approach and provide a deeper understanding of lepidopteran aging. More importantly, the results identify the key altered metabolic pathways that collectively contribute to the muscle aging phenotype and thereby improve our understanding of muscle senescence. |
format | Online Article Text |
id | pubmed-5772441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57724412018-01-26 A procession of metabolic alterations accompanying muscle senescence in Manduca sexta Wone, Bernard W. M. Kinchen, Jason M. Kaup, Elana R. Wone, Beate Sci Rep Article Biological aging profoundly impairs muscle function, performance, and metabolism. Because the progression of metabolic alterations associated with aging muscle has not been chronicled, we tracked the metabolic profiles of flight muscle from middle to advanced age in Manduca sexta to identify key molecules during the progression of muscle aging, as well as to evaluate the utility of the M. sexta system for molecular dissection of muscle aging. We identified a number of differences between Diel Time, Sexes, and Muscle Ages, including changes in metabolites related to energetics, extracellular matrix turnover, and glutathione metabolism. Increased abundances of glycolytic metabolites suggest a shift toward increased glycolysis with advancing age, whereas decreased abundances in lysolipids and acylcarnitines reflect decreasing beta-oxidation. We also observed a shift towards decreased polyamine metabolism with age, which might result in an age-related decline in lipid metabolism possibly due to regulation of energy metabolism by polyamines. Collectively, our findings demonstrate the feasibility of our system and approach and provide a deeper understanding of lepidopteran aging. More importantly, the results identify the key altered metabolic pathways that collectively contribute to the muscle aging phenotype and thereby improve our understanding of muscle senescence. Nature Publishing Group UK 2018-01-17 /pmc/articles/PMC5772441/ /pubmed/29343811 http://dx.doi.org/10.1038/s41598-018-19630-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wone, Bernard W. M. Kinchen, Jason M. Kaup, Elana R. Wone, Beate A procession of metabolic alterations accompanying muscle senescence in Manduca sexta |
title | A procession of metabolic alterations accompanying muscle senescence in Manduca sexta |
title_full | A procession of metabolic alterations accompanying muscle senescence in Manduca sexta |
title_fullStr | A procession of metabolic alterations accompanying muscle senescence in Manduca sexta |
title_full_unstemmed | A procession of metabolic alterations accompanying muscle senescence in Manduca sexta |
title_short | A procession of metabolic alterations accompanying muscle senescence in Manduca sexta |
title_sort | procession of metabolic alterations accompanying muscle senescence in manduca sexta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772441/ https://www.ncbi.nlm.nih.gov/pubmed/29343811 http://dx.doi.org/10.1038/s41598-018-19630-5 |
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