Glucagon-like peptide 1 (GLP-1)

Research output: Contribution to journalReviewpeer-review

Documents

  • T. D. Mueller
  • B. Finan
  • S. R. Bloom
  • D. D'Alessio
  • D. J. Drucker
  • P. R. Flatt
  • A. Fritsche
  • F. Gribble
  • H. J. Grill
  • J. F. Habener
  • W. Langhans
  • J. J. Meier
  • M. A. Nauck
  • D. Perez-Tilve
  • A. Pocai
  • F. Reimann
  • D. A. Sandoval
  • R. J. Seeley
  • K. Stemmer
  • M. Tang-Christensen
  • S. C. Woods
  • R. D. DiMarchi
  • M. H. Tschoep
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 beta-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 (C) 2019 The Authors. Published by Elsevier GmbH.
Original languageEnglish
JournalMolecular Metabolism
Volume30
Pages (from-to)72-130
ISSN2212-8778
DOIs
Publication statusPublished - 2019

    Research areas

  • GLP-1, Insulin, Glucagon, Diabetes, Obesity

Number of downloads are based on statistics from Google Scholar and www.ku.dk


No data available

ID: 232137365