Coronary heart disease and type-2 diabetes are both major global health burdens associated with an increased risk of myocardial infarction (MI). Following MI, ischaemia-reperfusion injury (IRI) remains a significant contributor to myocardial injury at the cellular level. Research has focussed on identifying a strategy or intervention to minimise IRI to optimise reperfusion therapy, with the aim of delivering a superior clinical outcome. The incretin hormone glucagon-like peptide-1, already an established basis for the treatment of type-2 diabetes, also has the potential to protect against IRI. We explain the physiology and cellular processes involved in IRI, and the intracellular pathways activated by GLP-1, which could intercept IRI and deliver cardioprotection. The review also examines the current preclinical and clinical evidence for GLP-1 in cardioprotection and future directions for research as we look for an effective adjunctive treatment to minimise IRI. © 2014 Clarke et al.; licensee BioMed Central Ltd.
CITATION STYLE
Clarke, S. J., McCormick, L. M., & Dutka, D. P. (2014, January 11). Optimising cardioprotection during myocardial ischaemia: Targeting potential intracellular pathways with glucagon-like peptide-1. Cardiovascular Diabetology. https://doi.org/10.1186/1475-2840-13-12
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