TY - JOUR
T1 - Effects of Acute and Chronic Resistance Exercise on the Skeletal Muscle Metabolome
AU - Gehlert, Sebastian
AU - Weinisch, Patrick
AU - Römisch-Margl, Werner
AU - Jaspers, Richard T
AU - Artati, Anna
AU - Adamski, Jerzy
AU - Dyar, Kenneth A
AU - Aussieker, Thorben
AU - Jacko, Daniel
AU - Bloch, Wilhelm
AU - Wackerhage, Henning
AU - Kastenmüller, Gabi
N1 - Copyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/5/16
Y1 - 2022/5/16
N2 - Resistance training promotes metabolic health and stimulates muscle
hypertrophy, but the precise routes by which resistance exercise (RE)
conveys these health benefits are largely unknown. Aim: To investigate
how acute RE affects human skeletal muscle metabolism. Methods: We
collected vastus lateralis biopsies from six healthy male untrained
volunteers at rest, before the first of 13 RE training sessions, and 45
min after the first and last bouts of RE. Biopsies were analysed using
untargeted mass spectrometry-based metabolomics. Results: We measured
617 metabolites covering a broad range of metabolic pathways. In the
untrained state RE altered 33 metabolites, including increased
3-methylhistidine and N-lactoylvaline, suggesting increased protein
breakdown, as well as metabolites linked to ATP (xanthosine) and NAD
(N1-methyl-2-pyridone-5-carboxamide) metabolism; the bile acid
chenodeoxycholate also increased in response to RE in muscle opposing
previous findings in blood. Resistance training led to muscle
hypertrophy, with slow type I and fast/intermediate type II muscle fibre
diameter increasing by 10.7% and 10.4%, respectively. Comparison of
post-exercise metabolite levels between trained and untrained state
revealed alterations of 46 metabolites, including decreased N-acetylated
ketogenic amino acids and increased beta-citrylglutamate which might
support growth. Only five of the metabolites that changed after acute
exercise in the untrained state were altered after chronic training,
indicating that training induces multiple metabolic changes not directly
related to the acute exercise response. Conclusion: The human skeletal
muscle metabolome is sensitive towards acute RE in the trained and
untrained states and reflects a broad range of adaptive processes in
response to repeated stimulation.
AB - Resistance training promotes metabolic health and stimulates muscle
hypertrophy, but the precise routes by which resistance exercise (RE)
conveys these health benefits are largely unknown. Aim: To investigate
how acute RE affects human skeletal muscle metabolism. Methods: We
collected vastus lateralis biopsies from six healthy male untrained
volunteers at rest, before the first of 13 RE training sessions, and 45
min after the first and last bouts of RE. Biopsies were analysed using
untargeted mass spectrometry-based metabolomics. Results: We measured
617 metabolites covering a broad range of metabolic pathways. In the
untrained state RE altered 33 metabolites, including increased
3-methylhistidine and N-lactoylvaline, suggesting increased protein
breakdown, as well as metabolites linked to ATP (xanthosine) and NAD
(N1-methyl-2-pyridone-5-carboxamide) metabolism; the bile acid
chenodeoxycholate also increased in response to RE in muscle opposing
previous findings in blood. Resistance training led to muscle
hypertrophy, with slow type I and fast/intermediate type II muscle fibre
diameter increasing by 10.7% and 10.4%, respectively. Comparison of
post-exercise metabolite levels between trained and untrained state
revealed alterations of 46 metabolites, including decreased N-acetylated
ketogenic amino acids and increased beta-citrylglutamate which might
support growth. Only five of the metabolites that changed after acute
exercise in the untrained state were altered after chronic training,
indicating that training induces multiple metabolic changes not directly
related to the acute exercise response. Conclusion: The human skeletal
muscle metabolome is sensitive towards acute RE in the trained and
untrained states and reflects a broad range of adaptive processes in
response to repeated stimulation.
U2 - 10.3390/metabo12050445
DO - 10.3390/metabo12050445
M3 - Journal articles
C2 - 35629949
SN - 2218-1989
VL - 12
SP - 1
EP - 21
JO - Metabolites
JF - Metabolites
IS - 5
M1 - 445
ER -