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RESEARCH PRODUCT

Changes in the spatial distribution of the Purkinje network after acute myocardial infarction in the pig

Maite IzquierdoVictor Garcia-bustosFrancisco J. ChorroAmparo Ruiz-sauriCesar Rios-navarroVicente BodíRafael Sebastian

subject

0301 basic medicineCritical Care and Emergency MedicineSwinemedicine.medical_treatmentMyocardial InfarctionInfarction030204 cardiovascular system & hematologyPathology and Laboratory MedicineVascular MedicinePurkinje Cells0302 clinical medicineAnimal CellsIschemiaMedicine and Health SciencesTissue DistributionMyocardial infarctionNeuronsCardiomyocytesMultidisciplinaryQRHeartInfarctionDisease ProgressionCardiologyMedicineCellular TypesAnatomyElectrical conduction system of the heartResearch Articlemedicine.medical_specialtyHistologyScienceCardiologyMuscle TissueIschemiaMyocardial Reperfusion InjuryCatheter ablation03 medical and health sciencesSigns and SymptomsHeart Conduction SystemDiagnostic MedicineInternal medicinemedicineAnimalscardiovascular diseasesEndocardiumMuscle Cellsbusiness.industryBiology and Life SciencesCell Biologymedicine.diseaseElectrophysiologyBiological Tissue030104 developmental biologyVacuolizationCellular NeuroscienceReperfusionCardiovascular AnatomyNerve NetbusinessEndocardiumNeuroscience

description

Purkinje cells (PCs) are more resistant to ischemia than myocardial cells, and are suspected to participate in ventricular arrhythmias following myocardial infarction (MI). Histological studies afford little evidence on the behavior and adaptation of PCs in the different stages of MI, especially in the chronic stage, and no quantitative data have been reported to date beyond subjective qualitative depictions. The present study uses a porcine model to present the first quantitative analysis of the distal cardiac conduction system and the first reported change in the spatial distribution of PCs in three representative stages of MI: an acute model both with and without reperfusion; a subacute model one week after reperfusion; and a chronic model one month after reperfusion. Purkinje cells are able to survive after 90 minutes of ischemia and subsequent reperfusion to a greater extent than cardiomyocytes. A decrease is observed in the number of PCs, which suffer reversible subcellular alterations such as cytoplasm vacuolization, together with redistribution from the mesocardium-the main localization of PCs in the heart of ungulate species-towards the endocardium and perivascular epicardial areas. However, these changes mainly occur during the first week after ischemia and reperfusion, and are maintained in the chronic stages. This anatomical substrate can explain the effectiveness of endo-epicardial catheter ablation of monomorphic ventricular tachycardias in the chronic scar after infarction, and sets a basis for further electrophysiological and molecular studies, and future therapeutic strategies.

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