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Updated: Jan 25, 2026

Quantifying Agonist Activity at G Protein-coupled Receptors
Published on: December 26, 2011
Glucagon-Like Peptide-1 Receptor Agonists and Strategies To Improve Their Efficiency
Seyed Ebrahim Alavi1, Peter J Cabot1, Peter M Moyle1
1School of Pharmacy , The University of Queensland , Woolloongabba , 4102 , Australia.
Abstract:
Type 2 diabetes mellitus (T2DM) is increasing in global prevalence and is associated with serious health problems (e.g., cardiovascular disease). Various treatment options are available for T2DM, including the incretin hormone glucagon-like peptide-1 (GLP-1). GLP-1 is a therapeutic peptide secreted from the intestines following food intake, which stimulates the secretion of insulin from the pancreas. The native GLP-1 has a very short plasma half-life, owning to renal clearance and degradation by the enzyme dipeptidyl peptidase-4. To overcome this issue, various GLP-1 agonists with increased resistance to proteolytic degradation and reduced renal clearance have been developed, with several currently marketed. Strategies, such as controlled release delivery systems, methods to reduce renal clearance (e.g., PEGylation and conjugation to antibodies), and methods to improve proteolytic stability (e.g., stapling, cyclization, and glycosylation) provide means to further improve the ability of GLP-1 analogs. These will be discussed in this literature review.
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