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dc.contributor.author | Dasi, Albert | es_ES |
dc.contributor.author | Climent, Andreu M. | es_ES |
dc.contributor.author | Martínez, Laura | es_ES |
dc.contributor.author | Gómez, Juan F. | es_ES |
dc.contributor.author | Ferrero De Loma-Osorio, José María | es_ES |
dc.contributor.author | Trenor Gomis, Beatriz Ana | es_ES |
dc.date.accessioned | 2022-02-17T07:20:52Z | |
dc.date.available | 2022-02-17T07:20:52Z | |
dc.date.issued | 2019-09-11 | es_ES |
dc.identifier.isbn | 978-1-7281-6936-1 | es_ES |
dc.identifier.issn | 2325-887X | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/180929 | |
dc.description.abstract | [EN] Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have proven to be crucial in pharmacological assessment. Nevertheless, their response to drugs when coupled forming a tissue is not fully understood. Thus, the aim of this study was to determine whether blocking L-type Ca+2 current (¿"#$) in a hiPSCCMs tissue could be considered as a potential antiarrhythmic procedure. To analyze the effects of ¿"#$ block, the maximum conductance of ¿"#$ (¿"#$) was decreased (block conditions) and compared to control. In both situations, control and block, the tissue was stimulated following a cross-field protocol to generate re-entries. A phase analysis was performed and specific parameters, such as re-entry frequency (¿'(()*'+), excitation wavelength, vulnerable window (VW), and cellular excitability, were evaluated. Induced re-entries, where ¿"#$ was reduced by 70% showed a 6.9% and a 47.83% decrease in ¿'(()*'+ and in the width of the VW, respectively. Our results suggest that blocking calcium channels could be considered as an antiarrhythmic strategy in a hiPSC-CMs tissue. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | IEEE | es_ES |
dc.relation.ispartof | 2019 Computing in Cardiology (CinC). Proceedings | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject.classification | TECNOLOGIA ELECTRONICA | es_ES |
dc.title | Blocking L-Type Calcium Current Reduces Vulnerability to Re-Entry in Human iPSC-Derived Cardiomyocytes Tissue | es_ES |
dc.type | Comunicación en congreso | es_ES |
dc.type | Artículo | es_ES |
dc.type | Capítulo de libro | es_ES |
dc.identifier.doi | 10.22489/CinC.2019.113 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/AEI//DPI2016-75799-R//TECNOLOGIAS COMPUTACIONALES PARA LA OPTIMIZACION DE TERAPIAS PERSONALIZADAS DE PATOLOGIAS AURICULARES Y VENTRICULARES/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Ingeniería Electrónica - Departament d'Enginyeria Electrònica | es_ES |
dc.description.bibliographicCitation | Dasi, A.; Climent, AM.; Martínez, L.; Gómez, JF.; Ferrero De Loma-Osorio, JM.; Trenor Gomis, BA. (2019). Blocking L-Type Calcium Current Reduces Vulnerability to Re-Entry in Human iPSC-Derived Cardiomyocytes Tissue. IEEE. 1-4. https://doi.org/10.22489/CinC.2019.113 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.conferencename | 46th Computing in Cardiology Conference (CinC 2019) | es_ES |
dc.relation.conferencedate | Septiembre 08-11,2019 | es_ES |
dc.relation.conferenceplace | Singapore | es_ES |
dc.relation.publisherversion | https://doi.org/10.22489/CinC.2019.113 | es_ES |
dc.description.upvformatpinicio | 1 | es_ES |
dc.description.upvformatpfin | 4 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.relation.pasarela | S\396365 | es_ES |