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GDF15 increases insulin action in the liver and adipose tissue via a ß-adrenergic receptor-mediated mechanism.
Sjøberg, Kim A; Sigvardsen, Casper M; Alvarado-Diaz, Abdiel; Andersen, Nicoline Resen; Larance, Mark; Seeley, Randy J; Schjerling, Peter; Knudsen, Jakob G; Katzilieris-Petras, Georgios; Clemmensen, Christoffer; Jørgensen, Sebastian Beck; De Bock, Katrien; Richter, Erik A.
Afiliação
  • Sjøberg KA; Department of Nutrition, Exercise, and Sports, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.
  • Sigvardsen CM; Department of Nutrition, Exercise, and Sports, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.
  • Alvarado-Diaz A; Laboratory of Exercise and Health, Department of Health Sciences and Technology, Swiss Federal Institute of Technology (ETH Zürich), Zurich, Switzerland.
  • Andersen NR; Department of Nutrition, Exercise, and Sports, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.
  • Larance M; Faculty of Medicine and Health, School of Medical Sciences, Charles Perkins Centre, University of Sydney, Sydney, Australia.
  • Seeley RJ; Department of Surgery, University of Michigan, Ann Arbor, MI, USA.
  • Schjerling P; Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Copenhagen, Denmark; Center for Healthy Aging, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Knudsen JG; Section for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
  • Katzilieris-Petras G; Section for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
  • Clemmensen C; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Jørgensen SB; Global Drug Discovery, Obesity Research, Novo Nordisk, Maaloev, Denmark; Bio Innovation Hub Transformational Research Unit, Novo Nordisk, Boston, MA, USA.
  • De Bock K; Laboratory of Exercise and Health, Department of Health Sciences and Technology, Swiss Federal Institute of Technology (ETH Zürich), Zurich, Switzerland. Electronic address: katrien-debock@ethz.ch.
  • Richter EA; Department of Nutrition, Exercise, and Sports, Faculty of Science, University of Copenhagen, Copenhagen, Denmark. Electronic address: erichter@nexs.ku.dk.
Cell Metab ; 35(8): 1327-1340.e5, 2023 08 08.
Article em En | MEDLINE | ID: mdl-37473755
ABSTRACT
Growth differentiation factor 15 (GDF15) induces weight loss and increases insulin action in obese rodents. Whether and how GDF15 improves insulin action without weight loss is unknown. Obese rats were treated with GDF15 and displayed increased insulin tolerance 5 h later. Lean and obese female and male mice were treated with GDF15 on days 1, 3, and 5 without weight loss and displayed increased insulin sensitivity during a euglycemic hyperinsulinemic clamp on day 6 due to enhanced suppression of endogenous glucose production and increased glucose uptake in WAT and BAT. GDF15 also reduced glucagon levels during clamp independently of the GFRAL receptor. The insulin-sensitizing effect of GDF15 was completely abrogated in GFRAL KO mice and also by treatment with the ß-adrenergic antagonist propranolol and in ß1,ß2-adrenergic receptor KO mice. GDF15 activation of the GFRAL receptor increases ß-adrenergic signaling, in turn, improving insulin action in the liver and white and brown adipose tissue.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistência à Insulina / Receptores Adrenérgicos beta Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistência à Insulina / Receptores Adrenérgicos beta Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article