"Fazeelat Mazhar, Francesco Regazzoni, C. Bartolucci, C. Corsi, L. Dede’, A. Quarteroni, S. Severi
{"title":"一种具有机械钙反馈效应的新型人心房机电心肌细胞模型","authors":"\"Fazeelat Mazhar, Francesco Regazzoni, C. Bartolucci, C. Corsi, L. Dede’, A. Quarteroni, S. Severi","doi":"10.22489/CinC.2022.195","DOIUrl":null,"url":null,"abstract":"Electromechanical coupling is crucial for modeling a realistic representation of $Ca^{+2}$ transient and $Ca^{+2}$ cycling. Cellular $Ca^{+2}$ dynamics in atria differ fundamentally from the ventricles. A biophysically detailed electrophysiology model is hence necessary to reproduce the experimentally observed phenomena like $Ca^{+2}$ wave propagation in human atrial myocytes. In this work, we present a novel detailed and yet computationally efficient electrophysiology model, its coupling with a contraction myofilament model and the effect of mechano-calcium feedback on coupling. This novel electromechanical model was calibrated for a collection of human atrial data and was evaluated by reproducing the rate adaptation property of action potential, $Ca^{+2}$ transient and the active force. The aim of this article is to present a new electromechanical model for human atrial myocyte and to analyse the mechanism behind the rate adaptation.","PeriodicalId":117840,"journal":{"name":"2022 Computing in Cardiology (CinC)","volume":"126 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Novel Human Atrial Electromechanical Cardiomyocyte Model with Mechano-Calcium Feedback Effect\",\"authors\":\"\\\"Fazeelat Mazhar, Francesco Regazzoni, C. Bartolucci, C. Corsi, L. Dede’, A. Quarteroni, S. Severi\",\"doi\":\"10.22489/CinC.2022.195\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Electromechanical coupling is crucial for modeling a realistic representation of $Ca^{+2}$ transient and $Ca^{+2}$ cycling. Cellular $Ca^{+2}$ dynamics in atria differ fundamentally from the ventricles. A biophysically detailed electrophysiology model is hence necessary to reproduce the experimentally observed phenomena like $Ca^{+2}$ wave propagation in human atrial myocytes. In this work, we present a novel detailed and yet computationally efficient electrophysiology model, its coupling with a contraction myofilament model and the effect of mechano-calcium feedback on coupling. This novel electromechanical model was calibrated for a collection of human atrial data and was evaluated by reproducing the rate adaptation property of action potential, $Ca^{+2}$ transient and the active force. The aim of this article is to present a new electromechanical model for human atrial myocyte and to analyse the mechanism behind the rate adaptation.\",\"PeriodicalId\":117840,\"journal\":{\"name\":\"2022 Computing in Cardiology (CinC)\",\"volume\":\"126 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2022 Computing in Cardiology (CinC)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22489/CinC.2022.195\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2022 Computing in Cardiology (CinC)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22489/CinC.2022.195","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Novel Human Atrial Electromechanical Cardiomyocyte Model with Mechano-Calcium Feedback Effect
Electromechanical coupling is crucial for modeling a realistic representation of $Ca^{+2}$ transient and $Ca^{+2}$ cycling. Cellular $Ca^{+2}$ dynamics in atria differ fundamentally from the ventricles. A biophysically detailed electrophysiology model is hence necessary to reproduce the experimentally observed phenomena like $Ca^{+2}$ wave propagation in human atrial myocytes. In this work, we present a novel detailed and yet computationally efficient electrophysiology model, its coupling with a contraction myofilament model and the effect of mechano-calcium feedback on coupling. This novel electromechanical model was calibrated for a collection of human atrial data and was evaluated by reproducing the rate adaptation property of action potential, $Ca^{+2}$ transient and the active force. The aim of this article is to present a new electromechanical model for human atrial myocyte and to analyse the mechanism behind the rate adaptation.