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Metabolomic Analysis of Skeletal Muscle in Aged Mice
Sarcopenia is the age-induced, progressive loss of skeletal muscle mass and function. To better understand changes in skeletal muscle during sarcopenia, we performed a metabolomic analysis of skeletal muscle in young (8-week-old) and aged (28-month-old) mice by using capillary electrophoresis with e...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639307/ https://www.ncbi.nlm.nih.gov/pubmed/31320689 http://dx.doi.org/10.1038/s41598-019-46929-8 |
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author | Uchitomi, Ran Hatazawa, Yukino Senoo, Nanami Yoshioka, Kiyoshi Fujita, Mariko Shimizu, Takahiko Miura, Shinji Ono, Yusuke Kamei, Yasutomi |
author_facet | Uchitomi, Ran Hatazawa, Yukino Senoo, Nanami Yoshioka, Kiyoshi Fujita, Mariko Shimizu, Takahiko Miura, Shinji Ono, Yusuke Kamei, Yasutomi |
author_sort | Uchitomi, Ran |
collection | PubMed |
description | Sarcopenia is the age-induced, progressive loss of skeletal muscle mass and function. To better understand changes in skeletal muscle during sarcopenia, we performed a metabolomic analysis of skeletal muscle in young (8-week-old) and aged (28-month-old) mice by using capillary electrophoresis with electrospray ionization time-of-flight mass spectrometry. Principal component analysis showed clear changes in metabolites between young and aged mice. Glucose metabolism products were decreased in aged mice, specifically fructose 1,6-diphosphate (0.4-fold) and dihydroxyacetone phosphate (0.6-fold), possibly from decreased glycolytic muscle fibers. Multiple metabolic products associated with phospholipid metabolism were significantly changed in aged mice, which may reflect changes in cell membrane phospholipids of skeletal muscle. Products of polyamine metabolism, which are known to increase nucleic acid and protein synthesis, decreased in spermine (0.5-fold) and spermidine (0.6-fold) levels. By contrast, neurotransmitter levels were increased in skeletal muscle of aged mice, including acetylcholine (1.8-fold), histamine (2.6-fold), and serotonin (1.7-fold). The increase in acetylcholine might compensate for age-associated dropout of neuromuscular junctions, whereas the increases in histamine and serotonin might be due to muscle injury associated with aging. Further analysis focusing on the altered metabolites observed in this study will provide essential data for understanding aging muscles. |
format | Online Article Text |
id | pubmed-6639307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66393072019-07-25 Metabolomic Analysis of Skeletal Muscle in Aged Mice Uchitomi, Ran Hatazawa, Yukino Senoo, Nanami Yoshioka, Kiyoshi Fujita, Mariko Shimizu, Takahiko Miura, Shinji Ono, Yusuke Kamei, Yasutomi Sci Rep Article Sarcopenia is the age-induced, progressive loss of skeletal muscle mass and function. To better understand changes in skeletal muscle during sarcopenia, we performed a metabolomic analysis of skeletal muscle in young (8-week-old) and aged (28-month-old) mice by using capillary electrophoresis with electrospray ionization time-of-flight mass spectrometry. Principal component analysis showed clear changes in metabolites between young and aged mice. Glucose metabolism products were decreased in aged mice, specifically fructose 1,6-diphosphate (0.4-fold) and dihydroxyacetone phosphate (0.6-fold), possibly from decreased glycolytic muscle fibers. Multiple metabolic products associated with phospholipid metabolism were significantly changed in aged mice, which may reflect changes in cell membrane phospholipids of skeletal muscle. Products of polyamine metabolism, which are known to increase nucleic acid and protein synthesis, decreased in spermine (0.5-fold) and spermidine (0.6-fold) levels. By contrast, neurotransmitter levels were increased in skeletal muscle of aged mice, including acetylcholine (1.8-fold), histamine (2.6-fold), and serotonin (1.7-fold). The increase in acetylcholine might compensate for age-associated dropout of neuromuscular junctions, whereas the increases in histamine and serotonin might be due to muscle injury associated with aging. Further analysis focusing on the altered metabolites observed in this study will provide essential data for understanding aging muscles. Nature Publishing Group UK 2019-07-18 /pmc/articles/PMC6639307/ /pubmed/31320689 http://dx.doi.org/10.1038/s41598-019-46929-8 Text en © The Author(s) 2019 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 Uchitomi, Ran Hatazawa, Yukino Senoo, Nanami Yoshioka, Kiyoshi Fujita, Mariko Shimizu, Takahiko Miura, Shinji Ono, Yusuke Kamei, Yasutomi Metabolomic Analysis of Skeletal Muscle in Aged Mice |
title | Metabolomic Analysis of Skeletal Muscle in Aged Mice |
title_full | Metabolomic Analysis of Skeletal Muscle in Aged Mice |
title_fullStr | Metabolomic Analysis of Skeletal Muscle in Aged Mice |
title_full_unstemmed | Metabolomic Analysis of Skeletal Muscle in Aged Mice |
title_short | Metabolomic Analysis of Skeletal Muscle in Aged Mice |
title_sort | metabolomic analysis of skeletal muscle in aged mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639307/ https://www.ncbi.nlm.nih.gov/pubmed/31320689 http://dx.doi.org/10.1038/s41598-019-46929-8 |
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