Glucagon-like peptide 1 (GLP-1).

Journal Article (Journal Article;Review)

BACKGROUND: The glucagon-like peptide-1 (GLP-1) is a multifaceted hormone with broad pharmacological potential. Among the numerous metabolic effects of GLP-1 are the glucose-dependent stimulation of insulin secretion, decrease of gastric emptying, inhibition of food intake, increase of natriuresis and diuresis, and modulation of rodent β-cell proliferation. GLP-1 also has cardio- and neuroprotective effects, decreases inflammation and apoptosis, and has implications for learning and memory, reward behavior, and palatability. Biochemically modified for enhanced potency and sustained action, GLP-1 receptor agonists are successfully in clinical use for the treatment of type-2 diabetes, and several GLP-1-based pharmacotherapies are in clinical evaluation for the treatment of obesity. SCOPE OF REVIEW: In this review, we provide a detailed overview on the multifaceted nature of GLP-1 and its pharmacology and discuss its therapeutic implications on various diseases. MAJOR CONCLUSIONS: Since its discovery, GLP-1 has emerged as a pleiotropic hormone with a myriad of metabolic functions that go well beyond its classical identification as an incretin hormone. The numerous beneficial effects of GLP-1 render this hormone an interesting candidate for the development of pharmacotherapies to treat obesity, diabetes, and neurodegenerative disorders.

Full Text

Duke Authors

Cited Authors

  • Müller, TD; Finan, B; Bloom, SR; D'Alessio, D; Drucker, DJ; Flatt, PR; Fritsche, A; Gribble, F; Grill, HJ; Habener, JF; Holst, JJ; Langhans, W; Meier, JJ; Nauck, MA; Perez-Tilve, D; Pocai, A; Reimann, F; Sandoval, DA; Schwartz, TW; Seeley, RJ; Stemmer, K; Tang-Christensen, M; Woods, SC; DiMarchi, RD; Tschöp, MH

Published Date

  • December 2019

Published In

Volume / Issue

  • 30 /

Start / End Page

  • 72 - 130

PubMed ID

  • 31767182

Pubmed Central ID

  • PMC6812410

Electronic International Standard Serial Number (EISSN)

  • 2212-8778

Digital Object Identifier (DOI)

  • 10.1016/j.molmet.2019.09.010


  • eng

Conference Location

  • Germany