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hal.structure.identifierModélisation et calculs pour l'électrophysiologie cardiaque [CARMEN]
dc.contributor.authorABBATE, Emanuela
hal.structure.identifierNumerical simulation of biological flows [REO]
dc.contributor.authorBOULAKIA, Muriel
hal.structure.identifierModélisation et calculs pour l'électrophysiologie cardiaque [CARMEN]
dc.contributor.authorCOUDIÈRE, Yves
hal.structure.identifierNumerical simulation of biological flows [REO]
dc.contributor.authorGERBEAU, Jean-Frédéric
hal.structure.identifierLIPZ [La Celle Saint-Cloud]
dc.contributor.authorZITOUN, Philippe
hal.structure.identifierModélisation et calculs pour l'électrophysiologie cardiaque [CARMEN]
dc.contributor.authorZEMZEMI, Nejib
dc.date.accessioned2024-04-04T03:09:48Z
dc.date.available2024-04-04T03:09:48Z
dc.date.issued2018
dc.identifier.issn1056-8719
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/193637
dc.description.abstractEnWe propose a mathematical approach for the analysis of drugs effects on the electrical activity of human induced pluripotent stem cell-derived car-diomyocytes (hiPSC-CMs) based on multi-electrode array (MEA) experiments. Our goal is to produce an in silico tool able to simulate drugs action in MEA/hiPSC-CM assays. The mathematical model takes into account the geometry of the MEA and the electrodes' properties. The electrical activity of the stem cells at the ion-channel level is governed by a system of ordinary differential equations (ODEs). The ODEs are coupled to the bidomain equations, describing the propagation of the electrical wave in the stem cells preparation. The field potential (FP) measured by the MEA is modeled by the extra-cellular potential of the bidomain equations. First, we propose a strategy allowing us to generate a field potential in good agreement with the experimental data. We show that we are able to reproduce realistic field potentials by introducing different scenarios of heterogeneity in the action potential. This heterogeneity reflects the differentiation atria/ventricles and the age of the cells. Second, we introduce a drug/ion channels interaction based on a pore block model. We conduct different simulations for five drugs (mexiletine, dofetilide, bepridil, ivabradine and BayK). We compare the simulation results with the field potential collected from experimental measurements. Different biomarkers computed on the FP are considered, including depolarization amplitude, repolarization delay, repolarization amplitude and depolarization-repolarization segment. The simulation results show that the model reflect properly the main effects of these drugs on the FP.
dc.description.sponsorshipModélisation, simulation et traitement du signal en électrophysiologie cardiaque - ANR-13-LAB1-0007
dc.language.isoen
dc.publisherElsevier
dc.subject.enCardiac electrophysiology
dc.subject.enMEA
dc.subject.enField potential
dc.subject.enhIPSC-CMs
dc.subject.enDrug modelling
dc.title.enIn silico assessment of the effects of various compounds in MEA/hiPSC-CM assays: Modelling and numerical simulations
dc.typeArticle de revue
dc.subject.halSciences du Vivant [q-bio]/Sciences pharmaceutiques/Pharmacologie
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologie/Cardiologie et système cardiovasculaire
dc.subject.halMathématiques [math]/Analyse numérique [math.NA]
bordeaux.journalJournal of Pharmacological and Toxicological Methods
bordeaux.page59-72
bordeaux.volume89
bordeaux.hal.laboratoriesInstitut de Mathématiques de Bordeaux (IMB) - UMR 5251*
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
bordeaux.institutionCNRS
bordeaux.peerReviewedoui
hal.identifierhal-01562673
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01562673v1
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