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Abstract Background The ability of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) to decrease certain microvascular events has called for the investigation of GLP-1 RAs against diabetic retinopathy (DR), but the evidence is limited

( G ) LDH release into coronary effluents from perfused WT mouse hearts, measured by ELISA at timed intervals between 10 and 40 minutes of reperfusion and normalized to coronary flow (mL/min/g heart weight) ( n = 3)

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