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Glucagon acutely regulates hepatic amino acid catabolism and the effect may be disturbed by steatosis

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  • Marie Winther-Sørensen
  • Katrine D Galsgaard
  • Alberto Santos
  • Samuel A J Trammell
  • Karolina Sulek
  • Rune E Kuhre
  • Jens Pedersen
  • Daniel B Andersen
  • Anna S Hassing
  • Morten Dall
  • Jonas T Treebak
  • Matthew P Gillum
  • Signe S Torekov
  • Johanne A Windeløv
  • Jenna E Hunt
  • Sasha A S Kjeldsen
  • Sara L Jepsen
  • Catherine G Vasilopoulou
  • Filip K Knop
  • Cathrine Ørskov
  • Mikkel P Werge
  • Hanne Cathrine Bisgaard
  • Peter Lykke Eriksen
  • Hendrik Vilstrup
  • Lise Lotte Gluud
  • Jens J Holst
  • Nicolai J Wewer Albrechtsen
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Objective: Glucagon is well known to regulate blood glucose but may be equally important for amino acid metabolism. Plasma levels of amino acids are regulated by glucagon-dependent mechanism(s), while amino acids stimulate glucagon secretion from alpha cells, completing the recently described liver-alpha cell axis. The mechanisms underlying the cycle and the possible impact of hepatic steatosis are unclear. Methods: We assessed amino acid clearance in vivo in mice treated with a glucagon receptor antagonist (GRA), transgenic mice with 95% reduction in alpha cells, and mice with hepatic steatosis. In addition, we evaluated urea formation in primary hepatocytes from ob/ob mice and humans, and we studied acute metabolic effects of glucagon in perfused rat livers. We also performed RNA sequencing on livers from glucagon receptor knock-out mice and mice with hepatic steatosis. Finally, we measured individual plasma amino acids and glucagon in healthy controls and in two independent cohorts of patients with biopsy-verified non-alcoholic fatty liver disease (NAFLD). Results: Amino acid clearance was reduced in mice treated with GRA and mice lacking endogenous glucagon (loss of alpha cells) concomitantly with reduced production of urea. Glucagon administration markedly changed the secretion of rat liver metabolites and within minutes increased urea formation in mice, in perfused rat liver, and in primary human hepatocytes. Transcriptomic analyses revealed that three genes responsible for amino acid catabolism (Cps1, Slc7a2, and Slc38a2) were downregulated both in mice with hepatic steatosis and in mice with deletion of the glucagon receptor. Cultured ob/ob hepatocytes produced less urea upon stimulation with mixed amino acids, and amino acid clearance was lower in mice with hepatic steatosis. Glucagon-induced ureagenesis was impaired in perfused rat livers with hepatic steatosis. Patients with NAFLD had hyperglucagonemia and increased levels of glucagonotropic amino acids, including alanine in particular. Both glucagon and alanine levels were reduced after diet-induced reduction in Homeostatic Model Assessment for Insulin Resistance (HOMA-IR, a marker of hepatic steatosis). Conclusions: Glucagon regulates amino acid metabolism both non-transcriptionally and transcriptionally. Hepatic steatosis may impair glucagon-dependent enhancement of amino acid catabolism.

OriginalsprogEngelsk
Artikelnummer101080
TidsskriftMolecular Metabolism
Vol/bind42
Sider (fra-til)101080
ISSN2212-8778
DOI
StatusUdgivet - 1 dec. 2020

Bibliografisk note

Copyright © 2020 The Author(s). Published by Elsevier GmbH.. All rights reserved.

ID: 60880983