Glucagon-like peptide 1 (GLP-1)

2019 Molecular Metabolism 1,536 citations

Abstract

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. 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. 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.

Keywords

Glucagon-like peptide-1Glucagon-like peptide-2GlucagonProglucagonIncretinPeptideChemistryInternal medicineDiabetes mellitusEndocrinologyMedicineInsulinBiochemistryType 2 diabetes

MeSH Terms

Blood GlucoseDiabetes MellitusType 2Gastric Inhibitory PolypeptideGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorGlucoseHumansHypoglycemic AgentsInsulinInsulin SecretionInsulin-Secreting CellsObesityReceptorsGlucagon

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Publication Info

Year
2019
Type
review
Volume
30
Pages
72-130
Citations
1536
Access
Closed

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Cite This

Timo D. Müller, Brian Finan, Stephen R. Bloom et al. (2019). Glucagon-like peptide 1 (GLP-1). Molecular Metabolism , 30 , 72-130. https://doi.org/10.1016/j.molmet.2019.09.010

Identifiers

DOI
10.1016/j.molmet.2019.09.010
PMID
31767182
PMCID
PMC6812410

Data Quality

Data completeness: 90%