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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...

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Autores principales: Uchitomi, Ran, Hatazawa, Yukino, Senoo, Nanami, Yoshioka, Kiyoshi, Fujita, Mariko, Shimizu, Takahiko, Miura, Shinji, Ono, Yusuke, Kamei, Yasutomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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