Time of Exercise Specifies the Impact on Muscle Metabolic Pathways and Systemic Energy Homeostasis.
Animals
Blotting, Western
Calorimetry, Indirect
Circadian Rhythm
/ physiology
Energy Metabolism
/ physiology
Glycolysis
/ genetics
Homeostasis
/ genetics
Hypoxia-Inducible Factor 1, alpha Subunit
/ genetics
Lipid Peroxidation
/ genetics
Male
Mass Spectrometry
Mice
Muscle, Skeletal
/ metabolism
Physical Conditioning, Animal
Sequence Analysis, RNA
Software
Transcriptome
/ genetics
HIF1α
circadian rhythms
energy homeostasis
exercise metabolism
glycolysis
lipid oxidation
metabolomics
skeletal muscle
transcriptomics
Journal
Cell metabolism
ISSN: 1932-7420
Titre abrégé: Cell Metab
Pays: United States
ID NLM: 101233170
Informations de publication
Date de publication:
02 07 2019
02 07 2019
Historique:
received:
31
08
2018
revised:
06
02
2019
accepted:
26
03
2019
pubmed:
23
4
2019
medline:
1
9
2020
entrez:
23
4
2019
Statut:
ppublish
Résumé
While the timing of food intake is important, it is unclear whether the effects of exercise on energy metabolism are restricted to unique time windows. As circadian regulation is key to controlling metabolism, understanding the impact of exercise performed at different times of the day is relevant for physiology and homeostasis. Using high-throughput transcriptomic and metabolomic approaches, we identify distinct responses of metabolic oscillations that characterize exercise in either the early rest phase or the early active phase in mice. Notably, glycolytic activation is specific to exercise at the active phase. At the molecular level, HIF1α, a central regulator of glycolysis during hypoxia, is selectively activated in a time-dependent manner upon exercise, resulting in carbohydrate exhaustion, usage of alternative energy sources, and adaptation of systemic energy expenditure. Our findings demonstrate that the time of day is a critical factor to amplify the beneficial impact of exercise on both metabolic pathways within skeletal muscle and systemic energy homeostasis.
Identifiants
pubmed: 31006592
pii: S1550-4131(19)30183-4
doi: 10.1016/j.cmet.2019.03.013
pii:
doi:
Substances chimiques
HIF1A protein, human
0
Hypoxia-Inducible Factor 1, alpha Subunit
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
92-110.e4Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.