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Pflugers Arch. 1998 Apr;435(5):583-94.

Cellular regulation of islet hormone secretion by the incretin hormone glucagon-like peptide 1.

Author information

1
Department of Islet Cell Physiology, Novo Nordisk A/S, The Symbion Science Park, Fruebjergvej 3, DK-2100 Copenhagen, Denmark.

Abstract

Glucagon-like peptide 1 is a gastrointestinally derived hormone with profound effects on nutrient-induced pancreatic hormone release. GLP-1 modulates insulin, glucagon and somatostatin secretion by binding to guanine nucleotide binding protein-coupled receptors resulting in the activation of adenylate cyclase and generation of cyclic adenosine monophosphate (cAMP). In the B-cell, cAMP, via activation of protein kinase A, interacts with a plethora of signal transduction processes including ion channel activity, intracellular Ca2+ handling and exocytosis of the insulin-containing granules. The stimulatory action of GLP-1 on insulin secretion, contrary to that of the currently used hypoglycaemic sulphonylureas, is glucose dependent and requires the presence of normal or elevated concentrations of the sugar. For this reason, GLP-1 attracts much interest as a possible novel principle for the treatment of human type-2 diabetes. Here we review the actions of GLP-1 on islet cell function and attempt to integrate current knowledge into a working model for the control of pancreatic hormone secretion.

PMID:
9479010
DOI:
10.1007/s004240050558
[Indexed for MEDLINE]

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