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They reduce neutrophil lifespan by upregulating the IFN--dependent death receptor Fas and regulating anti-apoptotic and pro-apoptotic protein expression to achieve a pro-apoptotic ratio

References Anitua E, Tierno R, Alkhraisat MH

Abstract We conducted a disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database (2005 Q22024 Q3) to evaluate neurological adverse events (NAEs) associated with six glucagon-like peptide-1 receptor agonists (GLP-1 RAs): exenatide, liraglutide, lixisenatide, dulaglutide, semaglutide, and tirzepatide

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