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Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart
A heart simulator, UT-Heart, is a finite element model of the human heart that can reproduce all the fundamental activities of the working heart, including propagation of excitation, contraction, and relaxation and generation of blood pressure and blood flow, based on the molecular aspects of the ca...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Physiological Society and The Korean Society of Pharmacology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717797/ https://www.ncbi.nlm.nih.gov/pubmed/31496866 http://dx.doi.org/10.4196/kjpp.2019.23.5.295 |
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author | Okada, Jun-ichi Washio, Takumi Sugiura, Seiryo Hisada, Toshiaki |
author_facet | Okada, Jun-ichi Washio, Takumi Sugiura, Seiryo Hisada, Toshiaki |
author_sort | Okada, Jun-ichi |
collection | PubMed |
description | A heart simulator, UT-Heart, is a finite element model of the human heart that can reproduce all the fundamental activities of the working heart, including propagation of excitation, contraction, and relaxation and generation of blood pressure and blood flow, based on the molecular aspects of the cardiac electrophysiology and excitation-contraction coupling. In this paper, we present a brief review of the practical use of UT-Heart. As an example, we focus on its application for predicting the effect of cardiac resynchronization therapy (CRT) and evaluating the proarrhythmic risk of drugs. Patient-specific, multiscale heart simulation successfully predicted the response to CRT by reproducing the complex pathophysiology of the heart. A proarrhythmic risk assessment system combining in vitro channel assays and in silico simulation of cardiac electrophysiology using UT-Heart successfully predicted druginduced arrhythmogenic risk. The assessment system was found to be reliable and efficient. We also developed a comprehensive hazard map on the various combinations of ion channel inhibitors. This in silico electrocardiogram database (now freely available at http://ut-heart.com/) can facilitate proarrhythmic risk assessment without the need to perform computationally expensive heart simulation. Based on these results, we conclude that the heart simulator, UT-Heart, could be a useful tool in clinical medicine and drug discovery. |
format | Online Article Text |
id | pubmed-6717797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Physiological Society and The Korean Society of Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67177972019-09-06 Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart Okada, Jun-ichi Washio, Takumi Sugiura, Seiryo Hisada, Toshiaki Korean J Physiol Pharmacol Review Article A heart simulator, UT-Heart, is a finite element model of the human heart that can reproduce all the fundamental activities of the working heart, including propagation of excitation, contraction, and relaxation and generation of blood pressure and blood flow, based on the molecular aspects of the cardiac electrophysiology and excitation-contraction coupling. In this paper, we present a brief review of the practical use of UT-Heart. As an example, we focus on its application for predicting the effect of cardiac resynchronization therapy (CRT) and evaluating the proarrhythmic risk of drugs. Patient-specific, multiscale heart simulation successfully predicted the response to CRT by reproducing the complex pathophysiology of the heart. A proarrhythmic risk assessment system combining in vitro channel assays and in silico simulation of cardiac electrophysiology using UT-Heart successfully predicted druginduced arrhythmogenic risk. The assessment system was found to be reliable and efficient. We also developed a comprehensive hazard map on the various combinations of ion channel inhibitors. This in silico electrocardiogram database (now freely available at http://ut-heart.com/) can facilitate proarrhythmic risk assessment without the need to perform computationally expensive heart simulation. Based on these results, we conclude that the heart simulator, UT-Heart, could be a useful tool in clinical medicine and drug discovery. The Korean Physiological Society and The Korean Society of Pharmacology 2019-09 2019-08-26 /pmc/articles/PMC6717797/ /pubmed/31496866 http://dx.doi.org/10.4196/kjpp.2019.23.5.295 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Okada, Jun-ichi Washio, Takumi Sugiura, Seiryo Hisada, Toshiaki Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart |
title | Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart |
title_full | Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart |
title_fullStr | Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart |
title_full_unstemmed | Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart |
title_short | Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart |
title_sort | clinical and pharmacological application of multiscale multiphysics heart simulator, ut-heart |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717797/ https://www.ncbi.nlm.nih.gov/pubmed/31496866 http://dx.doi.org/10.4196/kjpp.2019.23.5.295 |
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