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hal.structure.identifierModélisation et calculs pour l'électrophysiologie cardiaque [CARMEN]
dc.contributor.authorZEMZEMI, Nejib
hal.structure.identifierComputing Science Laboratory - Oxford University
dc.contributor.authorBLANCA, Rodriguez
dc.date.accessioned2024-04-04T03:20:39Z
dc.date.available2024-04-04T03:20:39Z
dc.date.issued2014-09-15
dc.identifier.issn1099-5129
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/194604
dc.description.abstractEnAims: Class III and IV drugs affect cardiac human ether-a-go-go related gene (IKr) and L-type calcium (ICaL) channels, resulting in complex alterations in repolarization with both anti- and pro-arrhythmic consequences. Interpretation of their effects on cellular and electrocardiogram (ECG)-based biomarkers for risk stratification is challenging. As pharmaceutical compounds often exhibit multiple ion channel effects, our goal is to investigate the simultaneous effect of ICaL and IKr block on human ventricular electrophysiology from ionic to ECG level. Methods and results: Simulations are conducted using a human body torso bidomain model, which includes realistic representation of human membrane kinetics, anatomy, and fibre orientation. A simple block pore model is incorporated to simulate drug-induced ICaL and IKr blocks, for drug dose = 0, IC50, 2× IC50, 10× IC50, and 30× IC50. Drug effects on human ventricular activity are quantified for different degrees and combinations of ICaL and IKr blocks from the ionic to the body surface ECG level. Electrocardiogram simulations show that ICaL block results in shortening of the QT interval, ST elevation, and reduced T-wave amplitude, caused by reduction in action potential duration and action potential amplitude during the plateau phase, and in repolarization times. In contrast, IKr block results in QT prolongation and reduced T-wave amplitude. When ICaL and IKr blocks are combined, the degree of ICaL block strongly determines QT interval whereas the effect of IKr block is more pronounced on the T-wave amplitude. Conclusion: Our simulation study provides new insights into the combined effect of ICaL and IKr blocks on human ventricular activity using a multiscale computational human torso model.
dc.language.isoen
dc.publisherOxford University Press (OUP)
dc.subject.enhERG block
dc.subject.enL-type calcium block
dc.subject.enQT interval
dc.subject.enECG modelling
dc.subject.enComputer simulation
dc.subject.enDispersion of repolarization
dc.title.enEffects of L-type calcium channel and human ether-a-go-go related gene blockers on the electrical activity of the human heart: a simulation study
dc.typeArticle de revue
dc.identifier.doi10.1093/europace/euu122
dc.subject.halSciences du Vivant [q-bio]/Bio-Informatique, Biologie Systémique [q-bio.QM]
dc.subject.halSciences du Vivant [q-bio]/Sciences pharmaceutiques/Médicaments
dc.subject.halMathématiques [math]/Analyse numérique [math.NA]
dc.subject.halMathématiques [math]/Equations aux dérivées partielles [math.AP]
dc.subject.halInformatique [cs]/Bio-informatique [q-bio.QM]
dc.subject.halInformatique [cs]/Modélisation et simulation
bordeaux.journalEP-Europace
bordeaux.hal.laboratoriesInstitut de Mathématiques de Bordeaux (IMB) - UMR 5251*
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
bordeaux.institutionCNRS
bordeaux.peerReviewedoui
hal.identifierhal-01064429
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01064429v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=EP-Europace&rft.date=2014-09-15&rft.eissn=1099-5129&rft.issn=1099-5129&rft.au=ZEMZEMI,%20Nejib&BLANCA,%20Rodriguez&rft.genre=article


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