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A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method

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A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method. / Brocklehurst, Paul; Adeniran, Ismail; Yang, Dongmin et al.
In: Biomed Research International, Vol. 2015, 854953, 25.10.2015.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Brocklehurst, P, Adeniran, I, Yang, D, Sheng, Y, Zhang, H & Ye, J 2015, 'A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method', Biomed Research International, vol. 2015, 854953. https://doi.org/10.1155/2015/854953

APA

Brocklehurst, P., Adeniran, I., Yang, D., Sheng, Y., Zhang, H., & Ye, J. (2015). A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method. Biomed Research International, 2015, Article 854953. https://doi.org/10.1155/2015/854953

Vancouver

Brocklehurst P, Adeniran I, Yang D, Sheng Y, Zhang H, Ye J. A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method. Biomed Research International. 2015 Oct 25;2015:854953. doi: 10.1155/2015/854953

Author

Brocklehurst, Paul ; Adeniran, Ismail ; Yang, Dongmin et al. / A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method. In: Biomed Research International. 2015 ; Vol. 2015.

Bibtex

@article{a735a60021d442f1b62f2064df582105,
title = "A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method",
abstract = "Cardiac tissue is a syncytium of coupled cells with pronounced intrinsic discrete nature. Previous models of cardiac electromechanics often ignore such discrete properties and treat cardiac tissue as a continuous medium, which has fundamental limitations. In the present study, we introduce a 2D electromechanical model for human atrial tissue based on the discrete element method (DEM). In the model, single-cell dynamics are governed by strongly coupling the electrophysiological model of Courtemanche et al. to the myofilament model of Rice et al. with two-way feedbacks. Each cell is treated as a viscoelastic body, which is physically represented by a clump of nine particles. Cell aggregations are arranged so that the anisotropic nature of cardiac tissue due to fibre orientations can be modelled. Each cell is electrically coupled to neighbouring cells, allowing excitation waves to propagate through the tissue. Cell-to-cell mechanical interactions are modelled using a linear contact bond model in DEM. By coupling cardiac electrophysiology with mechanics via the intracellular Ca2+ concentration, the DEM model successfully simulates the conduction of cardiac electrical waves and the tissue{\textquoteright}s corresponding mechanical contractions. The developed DEM model is numerically stable and provides a powerful method for studying the electromechanical coupling problem in the heart.",
author = "Paul Brocklehurst and Ismail Adeniran and Dongmin Yang and Yong Sheng and Henggui Zhang and Jianqiao Ye",
year = "2015",
month = oct,
day = "25",
doi = "10.1155/2015/854953",
language = "English",
volume = "2015",
journal = "Biomed Research International",
issn = "2314-6133",
publisher = "HINDAWI LTD",

}

RIS

TY - JOUR

T1 - A 2D Electromechanical Model of Human Atrial Tissue Using the Discrete Element Method

AU - Brocklehurst, Paul

AU - Adeniran, Ismail

AU - Yang, Dongmin

AU - Sheng, Yong

AU - Zhang, Henggui

AU - Ye, Jianqiao

PY - 2015/10/25

Y1 - 2015/10/25

N2 - Cardiac tissue is a syncytium of coupled cells with pronounced intrinsic discrete nature. Previous models of cardiac electromechanics often ignore such discrete properties and treat cardiac tissue as a continuous medium, which has fundamental limitations. In the present study, we introduce a 2D electromechanical model for human atrial tissue based on the discrete element method (DEM). In the model, single-cell dynamics are governed by strongly coupling the electrophysiological model of Courtemanche et al. to the myofilament model of Rice et al. with two-way feedbacks. Each cell is treated as a viscoelastic body, which is physically represented by a clump of nine particles. Cell aggregations are arranged so that the anisotropic nature of cardiac tissue due to fibre orientations can be modelled. Each cell is electrically coupled to neighbouring cells, allowing excitation waves to propagate through the tissue. Cell-to-cell mechanical interactions are modelled using a linear contact bond model in DEM. By coupling cardiac electrophysiology with mechanics via the intracellular Ca2+ concentration, the DEM model successfully simulates the conduction of cardiac electrical waves and the tissue’s corresponding mechanical contractions. The developed DEM model is numerically stable and provides a powerful method for studying the electromechanical coupling problem in the heart.

AB - Cardiac tissue is a syncytium of coupled cells with pronounced intrinsic discrete nature. Previous models of cardiac electromechanics often ignore such discrete properties and treat cardiac tissue as a continuous medium, which has fundamental limitations. In the present study, we introduce a 2D electromechanical model for human atrial tissue based on the discrete element method (DEM). In the model, single-cell dynamics are governed by strongly coupling the electrophysiological model of Courtemanche et al. to the myofilament model of Rice et al. with two-way feedbacks. Each cell is treated as a viscoelastic body, which is physically represented by a clump of nine particles. Cell aggregations are arranged so that the anisotropic nature of cardiac tissue due to fibre orientations can be modelled. Each cell is electrically coupled to neighbouring cells, allowing excitation waves to propagate through the tissue. Cell-to-cell mechanical interactions are modelled using a linear contact bond model in DEM. By coupling cardiac electrophysiology with mechanics via the intracellular Ca2+ concentration, the DEM model successfully simulates the conduction of cardiac electrical waves and the tissue’s corresponding mechanical contractions. The developed DEM model is numerically stable and provides a powerful method for studying the electromechanical coupling problem in the heart.

U2 - 10.1155/2015/854953

DO - 10.1155/2015/854953

M3 - Journal article

VL - 2015

JO - Biomed Research International

JF - Biomed Research International

SN - 2314-6133

M1 - 854953

ER -