Targeting the Incretin/Glucagon System With Triagonists to Treat Diabetes.

Journal Article (Journal Article;Review)

Glucagonlike peptide 1 (GLP-1) receptor agonists have been efficacious for the treatment of type 2 diabetes due to their ability to reduce weight and attenuate hyperglycemia. However, the activity of glucagonlike peptide 1 receptor-directed strategies is submaximal, and the only potent, sustainable treatment of metabolic dysfunction is bariatric surgery, necessitating the development of unique therapeutics. GLP-1 is structurally related to glucagon and glucose-dependent insulinotropic peptide (GIP), allowing for the development of intermixed, unimolecular peptides with activity at each of their respective receptors. In this review, we discuss the range of tissue targets and added benefits afforded by the inclusion of each of GIP and glucagon. We discuss considerations for the development of sequence-intermixed dual agonists and triagonists, highlighting the importance of evaluating balanced signaling at the targeted receptors. Several multireceptor agonist peptides have been developed and evaluated, and the key preclinical and clinical findings are reviewed in detail. The biological activity of these multireceptor agonists are founded in the success of GLP-1-directed strategies; by including GIP and glucagon components, these multireceptor agonists are thought to enhance GLP-1's activities by broadening the tissue targets and synergizing at tissues that express multiple receptors, such at the brain and pancreatic islet β cells. The development and utility of balanced, unimolecular multireceptor agonists provide both a useful tool for querying the actions of incretins and glucagon during metabolic disease and a unique drug class to treat type 2 diabetes with unprecedented efficacy.

Full Text

Duke Authors

Cited Authors

  • Capozzi, ME; DiMarchi, RD; Tschöp, MH; Finan, B; Campbell, JE

Published Date

  • October 1, 2018

Published In

Volume / Issue

  • 39 / 5

Start / End Page

  • 719 - 738

PubMed ID

  • 29905825

Pubmed Central ID

  • PMC7263842

Electronic International Standard Serial Number (EISSN)

  • 1945-7189

Digital Object Identifier (DOI)

  • 10.1210/er.2018-00117


  • eng

Conference Location

  • United States