TY - JOUR
T1 - Human skeletal muscle disuse atrophy has profound and negative effects on the muscle metabolome and lipidome
AU - Kilroe, Sean P.
AU - Von Ruff, Zachary D.
AU - Arentson-Lantz, Emily J.
AU - Romsdahl, Trevor B.
AU - Linares, Jennifer J.
AU - Kalenta, Hanna
AU - Marchant, Erik D.
AU - Volpi, Elena
AU - Paddon-Jones, Douglas
AU - Russell, William K.
AU - Rasmussen, Blake
N1 - Publisher Copyright:
Copyright © 2025 The Authors.
PY - 2025/6
Y1 - 2025/6
N2 - We investigated how short-term muscle disuse altered the skeletal muscle metabolome, lipidome, and transcriptome in middle-aged adults. We report that the energy metabolism pathways: nicotinate and nicotinamide metabolism, glycolysis, and TCA cycle, were reduced after 7 days of muscle disuse. These changes in the metabolome were reflected by changes in the transcriptome where multiple genes involved in glycolysis and TCA pathways were reduced after short-term disuse. Phenylalanine, tyrosine, and tryptophan metabolism pathways showed the same response and were reduced after short-term disuse. The skeletal muscle lipidome showed a decrease in phosphatidylinositols but an increase in phosphatidylglycerols and diacylglycerols after short-term muscle disuse. We conclude that short-term muscle disuse in humans has profound and negative effects on the muscle metabolome and lipidome. These include significant downregulation of muscle glycolytic, amino acid, and TCA cycle intermediates. In contrast, skeletal muscle lipids had a divergent response to disuse (e.g., increased phosphatidylglycerols and diacylglycerols, but reduced phosphatidylinositols).
AB - We investigated how short-term muscle disuse altered the skeletal muscle metabolome, lipidome, and transcriptome in middle-aged adults. We report that the energy metabolism pathways: nicotinate and nicotinamide metabolism, glycolysis, and TCA cycle, were reduced after 7 days of muscle disuse. These changes in the metabolome were reflected by changes in the transcriptome where multiple genes involved in glycolysis and TCA pathways were reduced after short-term disuse. Phenylalanine, tyrosine, and tryptophan metabolism pathways showed the same response and were reduced after short-term disuse. The skeletal muscle lipidome showed a decrease in phosphatidylinositols but an increase in phosphatidylglycerols and diacylglycerols after short-term muscle disuse. We conclude that short-term muscle disuse in humans has profound and negative effects on the muscle metabolome and lipidome. These include significant downregulation of muscle glycolytic, amino acid, and TCA cycle intermediates. In contrast, skeletal muscle lipids had a divergent response to disuse (e.g., increased phosphatidylglycerols and diacylglycerols, but reduced phosphatidylinositols).
KW - disuse atrophy
KW - human skeletal muscle
KW - lipidomics
KW - metabolomics
KW - transcriptomics
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U2 - 10.1152/ajpendo.00012.2025
DO - 10.1152/ajpendo.00012.2025
M3 - Article
C2 - 40298387
AN - SCOPUS:105006578242
SN - 0193-1849
VL - 328
SP - E962-E978
JO - American Journal of Physiology - Endocrinology and Metabolism
JF - American Journal of Physiology - Endocrinology and Metabolism
IS - 6
ER -