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3D Finite Element Electrical Model of Larval Zebrafish ECG Signals

Assessment of heart function in zebrafish larvae using electrocardiography (ECG) is a potentially useful tool in developing cardiac treatments and the assessment of drug therapies. In order to better understand how a measured ECG waveform is related to the structure of the heart, its position within...

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Autores principales: Crowcombe, James, Dhillon, Sundeep Singh, Hurst, Rhiannon Mary, Egginton, Stuart, Müller, Ferenc, Sík, Attila, Tarte, Edward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100939/
https://www.ncbi.nlm.nih.gov/pubmed/27824910
http://dx.doi.org/10.1371/journal.pone.0165655
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author Crowcombe, James
Dhillon, Sundeep Singh
Hurst, Rhiannon Mary
Egginton, Stuart
Müller, Ferenc
Sík, Attila
Tarte, Edward
author_facet Crowcombe, James
Dhillon, Sundeep Singh
Hurst, Rhiannon Mary
Egginton, Stuart
Müller, Ferenc
Sík, Attila
Tarte, Edward
author_sort Crowcombe, James
collection PubMed
description Assessment of heart function in zebrafish larvae using electrocardiography (ECG) is a potentially useful tool in developing cardiac treatments and the assessment of drug therapies. In order to better understand how a measured ECG waveform is related to the structure of the heart, its position within the larva and the position of the electrodes, a 3D model of a 3 days post fertilisation (dpf) larval zebrafish was developed to simulate cardiac electrical activity and investigate the voltage distribution throughout the body. The geometry consisted of two main components; the zebrafish body was modelled as a homogeneous volume, while the heart was split into five distinct regions (sinoatrial region, atrial wall, atrioventricular band, ventricular wall and heart chambers). Similarly, the electrical model consisted of two parts with the body described by Laplace’s equation and the heart using a bidomain ionic model based upon the Fitzhugh-Nagumo equations. Each region of the heart was differentiated by action potential (AP) parameters and activation wave conduction velocities, which were fitted and scaled based on previously published experimental results. ECG measurements in vivo at different electrode recording positions were then compared to the model results. The model was able to simulate action potentials, wave propagation and all the major features (P wave, R wave, T wave) of the ECG, as well as polarity of the peaks observed at each position. This model was based upon our current understanding of the structure of the normal zebrafish larval heart. Further development would enable us to incorporate features associated with the diseased heart and hence assist in the interpretation of larval zebrafish ECGs in these conditions.
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spelling pubmed-51009392016-11-18 3D Finite Element Electrical Model of Larval Zebrafish ECG Signals Crowcombe, James Dhillon, Sundeep Singh Hurst, Rhiannon Mary Egginton, Stuart Müller, Ferenc Sík, Attila Tarte, Edward PLoS One Research Article Assessment of heart function in zebrafish larvae using electrocardiography (ECG) is a potentially useful tool in developing cardiac treatments and the assessment of drug therapies. In order to better understand how a measured ECG waveform is related to the structure of the heart, its position within the larva and the position of the electrodes, a 3D model of a 3 days post fertilisation (dpf) larval zebrafish was developed to simulate cardiac electrical activity and investigate the voltage distribution throughout the body. The geometry consisted of two main components; the zebrafish body was modelled as a homogeneous volume, while the heart was split into five distinct regions (sinoatrial region, atrial wall, atrioventricular band, ventricular wall and heart chambers). Similarly, the electrical model consisted of two parts with the body described by Laplace’s equation and the heart using a bidomain ionic model based upon the Fitzhugh-Nagumo equations. Each region of the heart was differentiated by action potential (AP) parameters and activation wave conduction velocities, which were fitted and scaled based on previously published experimental results. ECG measurements in vivo at different electrode recording positions were then compared to the model results. The model was able to simulate action potentials, wave propagation and all the major features (P wave, R wave, T wave) of the ECG, as well as polarity of the peaks observed at each position. This model was based upon our current understanding of the structure of the normal zebrafish larval heart. Further development would enable us to incorporate features associated with the diseased heart and hence assist in the interpretation of larval zebrafish ECGs in these conditions. Public Library of Science 2016-11-08 /pmc/articles/PMC5100939/ /pubmed/27824910 http://dx.doi.org/10.1371/journal.pone.0165655 Text en © 2016 Crowcombe et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Crowcombe, James
Dhillon, Sundeep Singh
Hurst, Rhiannon Mary
Egginton, Stuart
Müller, Ferenc
Sík, Attila
Tarte, Edward
3D Finite Element Electrical Model of Larval Zebrafish ECG Signals
title 3D Finite Element Electrical Model of Larval Zebrafish ECG Signals
title_full 3D Finite Element Electrical Model of Larval Zebrafish ECG Signals
title_fullStr 3D Finite Element Electrical Model of Larval Zebrafish ECG Signals
title_full_unstemmed 3D Finite Element Electrical Model of Larval Zebrafish ECG Signals
title_short 3D Finite Element Electrical Model of Larval Zebrafish ECG Signals
title_sort 3d finite element electrical model of larval zebrafish ecg signals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100939/
https://www.ncbi.nlm.nih.gov/pubmed/27824910
http://dx.doi.org/10.1371/journal.pone.0165655
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