Glucagon revisited: Coordinated actions on the liver and kidney. (December 2018)

• Record Type: Journal Article
• Authors: Bankir, Lise; Bouby, Nadine; Speth, Robert C.; Velho, Gilberto; Crambert, Gilles
• Is Part Of: Diabetes research and clinical practice. Volume 146(2018)
• Page Start: 119
• Page End: 129
• Publication Date: 2018-12
• Subjects: Insulin -- Cyclic AMP -- Glycemia -- Gluconeogenesis -- Protein metabolism -- Urea -- Glucagon receptors; Diabetes -- Periodicals; Diabetes Mellitus -- Periodicals; 616.462
• DOI: 10.1016/j.diabres.2018.10.004
• Languages: English
• ISSNs: 0168-8227

Abstract

Abstract: Glucagon secretion is stimulated by a low plasma glucose concentration. By activating glycogenolysis and gluconeogenesis in the liver, glucagon contributes to maintain a normal glycemia. Glucagon secretion is also stimulated by the intake of proteins, and glucagon contributes to amino acid metabolism and nitrogen excretion. Amino acids are used for gluconeogenesis and ureagenesis, two metabolic pathways that are closely associated. Intriguingly, cyclic AMP, the second messenger of glucagon action in the liver, is released into the bloodstream becoming an extracellular messenger. These effects depend not only on glucagon itself but on the actual glucagon/insulin ratio because insulin counteracts glucagon action on the liver. This review revisits the role of glucagon in nitrogen metabolism and in disposal of nitrogen wastes. This role involves coordinated actions of glucagon on the liver and kidney. Glucagon influences the transport of fluid and solutes in the distal tubule and collecting duct, and extracellular cAMP influences proximal tubule reabsorption. These combined effects increase the fractional excretion of urea, sodium, potassium and phosphates. Moreover, the simultaneous actions of glucagon and extracellular cAMP are responsible, at least in part, for the protein-induced rise in glomerular filtration rate that contributes to a more efficient excretion of protein-derived end products.