Exercise training adaptations in liver glycogen and glycerolipids require hepatic AMP-activated protein kinase in mice.

aerobic exercise gluconeogenesis glycogenolysis metabolic flux analysis mitochondrial oxidative metabolism

Journal

American journal of physiology. Endocrinology and metabolism
ISSN: 1522-1555
Titre abrégé: Am J Physiol Endocrinol Metab
Pays: United States
ID NLM: 100901226

Informations de publication

Date de publication:
01 Jan 2024
Historique:
pubmed: 8 11 2023
medline: 8 11 2023
entrez: 8 11 2023
Statut: ppublish

Résumé

Regular exercise elicits adaptations in glucose and lipid metabolism that allow the body to meet energy demands of subsequent exercise bouts more effectively and mitigate metabolic diseases including fatty liver. Energy discharged during the acute exercise bouts that comprise exercise training may be a catalyst for liver adaptations. During acute exercise, liver glycogenolysis and gluconeogenesis are accelerated to supply glucose to working muscle. Lower liver energy state imposed by gluconeogenesis and related pathways activates AMP-activated protein kinase (AMPK), which conserves ATP partly by promoting lipid oxidation. This study tested the hypothesis that AMPK is necessary for liver glucose and lipid adaptations to training. Liver-specific AMPKα1α2 knockout (

Identifiants

pubmed: 37938177
doi: 10.1152/ajpendo.00289.2023
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

E14-E28

Subventions

Organisme : HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ID : DK050277
Organisme : HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ID : DK054902
Organisme : HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ID : DK059637
Organisme : HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ID : DK020593
Organisme : HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ID : DK136772

Auteurs

Curtis C Hughey (CC)

Division of Molecular Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States.
Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, United States.

Deanna P Bracy (DP)

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, United States.
Mouse Metabolic Phenotyping Center, Vanderbilt University, Nashville, Tennessee, United States.

Ferrol I Rome (FI)

Division of Molecular Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States.

Mickael Goelzer (M)

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, United States.

E Patrick Donahue (EP)

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, United States.

Benoit Viollet (B)

Université Paris Cité, CNRS, Inserm, Institut Cochin, Paris, France.

Marc Foretz (M)

Université Paris Cité, CNRS, Inserm, Institut Cochin, Paris, France.

David H Wasserman (DH)

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, United States.
Mouse Metabolic Phenotyping Center, Vanderbilt University, Nashville, Tennessee, United States.

Classifications MeSH