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pyroglutamyl apelin-13 amide (also known as (pGlu)apelin-13 amide) is a stable, enzyme-resistant peptide analogue of the endogenous adipokine apelin-13. Developed by researchers at Ulster University, it acts as an agonist of the apelin receptor (APLNR/APJ). Unlike native apelin-13, which has an extremely short biological half-life, this analogue is modified at the N-terminus with a pyroglutamyl group and at the C-terminus with an amide group to enhance enzymatic stability and prolong its circulating half-life. In preclinical models of type 2 diabetes and obesity, such as diet-induced obese (DIO) mice and db/db mice, chronic administration of pyroglutamyl apelin-13 amide has demonstrated significant antidiabetic and metabolic benefits, including improved glucose tolerance, enhanced insulin sensitivity, reduced glycated hemoglobin (HbA1c), decreased plasma triglycerides, and beneficial effects on pancreatic islet cell morphology.
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