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GLP-1R agonists have been tested in preclinical and clinical studies to investigate whether restoring brain insulin signaling is a viable treatment option for neuroinflammation and corresponding neurodegeneration
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A key challenge in studying native GLP-1 is its extremely short in vivo half-life of approximately 1–2 minutes, owing to rapid inactivation by dipeptidyl peptidase-4 (DPP-4), which cleaves the N-terminal His-Ala dipeptide from GLP-1 to produce the inactive metabolite GLP-1(9–36)amide
