Abstract Introduction Ejection fraction (EF) is an important predictor of cardiovascular morbidity and mortality after myocardial infarction (MI). Advanced therapies (specifically cardiosphere-derived cells-CDCs- or their secretome –S-CDCs) could be useful in this scenario. Our objective was to evaluate whether intracoronary (IC) administration of CDCs or S-CDCs could improve cardiac function in a porcine model of severe post-MI ventricular dysfunction. Methods A reperfused MI model was induced in Large White pigs. Animals with an EF<30% on day 7 post-MI received, in a blinded manner, 30x106 CDCs (n=7), 9.16 mg S-CDCs (n=6) or 5 ml of saline (n= 6) via IC route. Two magnetic resonance imaging studies were performed, on day 7 (to verify the inclusion criteria) and at 10 weeks, calculating: EF, indexed end systolic (ESVi) and diastolic (EDVi) volumes and infarct size. Results No significant differences in cardiac function were observed between the groups at 10 weeks. The S-CDCs group showed the best results in terms of cardiac function, with EF at 24±2% vs 29±3% vs 21±3%, EDVi at 104±8 ml/m² vs 95±8 ml/m² vs 107±9 ml/m², ESVi at 79±7 ml/m² vs 68±8 ml/m² vs 86±10 ml/m², and infarct size at 10±1% vs 11±2% vs 10±2% in the Control, S-CDCs, and CDCs groups, respectively. Conclusion In this experimental model of severe post-MI ventricular dysfunction, the administration of the assayed advanced therapies does not seem to be clinically advantageous, although the use of secretome could slightly improve overall ventricular function.
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