Multi-dimensional metabolomic remodeling under diverse muscle atrophic stimuli in vivo

Muscle wasting leads to reduced activities of daily living, an increased number of care-dependent individuals, and increased mortality. However, the metabolomic adaptations underlying muscle wasting remain poorly understood. Here, by comparing physiological, genetically induced, pathological, and age-related muscle atrophy, we identify the metabolites modulated by muscle atrophic stimuli, which we term "atrometabolites." Integrated metabolomics reveal that dysfunctional polyamine synthesis is a common feature of muscle atrophy. Mechanistically, we identify that adenosylmethionine decarboxylase 1 (Amd1) and Amd2 are important for maintaining polyamine metabolism and that downregulation of Amd1 and Amd2 is a trigger of myotube atrophy. Using skeletal muscle-specific FoxO triple-knockout mice, we find that FoxOs are required for immobilization-induced metabolomic remodeling and identify FoxO-dependent atrometabolites. This study comprehensively elucidates the molecular basis of muscle metabolomic adaptation and provides the datasets that will lead to the discovery of mechanisms underlying tissue adaptation to maintain homeostasis.

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Publication Details

Journal
Cell Reports
Published
2025-08-01
DOI
https://doi.org/10.1016/j.celrep.2025.116097
Citations
1
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.81

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article

Multi-dimensional metabolomic remodeling under diverse muscle atrophic stimuli in vivo

Tomoki Sato, Shinji Miura, Runa Kawaguchi, Hitoshi Gotoh et al.
1 citations
Cell Reports
Muscle Physiology and Disorders
0.81
article

Multi-dimensional metabolomic remodeling under diverse muscle atrophic stimuli in vivo

Tomoki Sato, Shinji Miura, Runa Kawaguchi, Hitoshi Gotoh, Naoki Ito, Mamoru Oyabu, Takahiro Eguchi, Yoshihiro Ogawa, Yasutomi Kamei, Tatsuya Yoshizawa, Kiyoshi Yoshioka, Yusuke Ono
article en
1 citations

Abstract

Muscle wasting leads to reduced activities of daily living, an increased number of care-dependent individuals, and increased mortality. However, the metabolomic adaptations underlying muscle wasting remain poorly understood. Here, by comparing physiological, genetically induced, pathological, and age-related muscle atrophy, we identify the metabolites modulated by muscle atrophic stimuli, which we term "atrometabolites." Integrated metabolomics reveal that dysfunctional polyamine synthesis is a common feature of muscle atrophy. Mechanistically, we identify that adenosylmethionine decarboxylase 1 (Amd1) and Amd2 are important for maintaining polyamine metabolism and that downregulation of Amd1 and Amd2 is a trigger of myotube atrophy. Using skeletal muscle-specific FoxO triple-knockout mice, we find that FoxOs are required for immobilization-induced metabolomic remodeling and identify FoxO-dependent atrometabolites. This study comprehensively elucidates the molecular basis of muscle metabolomic adaptation and provides the datasets that will lead to the discovery of mechanisms underlying tissue adaptation to maintain homeostasis.

Cell ReportsVol. 44(8)
Kyushu University (JP), University of Shizuoka (JP), Kyoto Prefectural University (JP), Kyoto Prefectural University of Medicine (JP), National Center for Geriatrics and Gerontology (JP)
Naito Foundation, Nakatomi Foundation, Uehara Memorial Foundation, Meiji Yasuda Life Foundation of Health and Welfare, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 25%
Muscle Physiology and Disorders
0.81
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