Format

Send to

Choose Destination

See 1 citation found by title matching your search:

J Biomech. 2016 Aug 16;49(12):2428-35. doi: 10.1016/j.jbiomech.2016.01.039. Epub 2016 Feb 11.

Sample-specific adaption of an improved electro-mechanical model of in vitro cardiac tissue.

Author information

1
Aachen University of Applied Sciences, Institute of Bioengineering, Biomechanics Lab, Heinrich-Mußmann-Straße 1, 52428 Jülich, Germany.
2
Aachen University of Applied Sciences, Institute of Bioengineering, Lab of Medical and Molecular Biology, Heinrich-Mußmann-Straße 1, 52428 Jülich, Germany.
3
Axiogenesis AG, Nattermannallee 1, 50829 Cologne, Germany.
4
Aachen University of Applied Sciences, Institute of Bioengineering, Biomechanics Lab, Heinrich-Mußmann-Straße 1, 52428 Jülich, Germany. Electronic address: m.staat@fh-aachen.de.

Abstract

We present an electromechanically coupled computational model for the investigation of a thin cardiac tissue construct consisting of human-induced pluripotent stem cell-derived atrial, ventricular and sinoatrial cardiomyocytes. The mechanical and electrophysiological parts of the finite element model, as well as their coupling are explained in detail. The model is implemented in the open source finite element code Code_Aster and is employed for the simulation of a thin circular membrane deflected by a monolayer of autonomously beating, circular, thin cardiac tissue. Two cardio-active drugs, S-Bay K8644 and veratridine, are applied in experiments and simulations and are investigated with respect to their chronotropic effects on the tissue. These results demonstrate the potential of coupled micro- and macroscopic electromechanical models of cardiac tissue to be adapted to experimental results at the cellular level. Further model improvements are discussed taking into account experimentally measurable quantities that can easily be extracted from the obtained experimental results. The goal is to estimate the potential to adapt the presented model to sample specific cell cultures.

KEYWORDS:

Cardiac tissue; Computational biomechanics; Drug simulation; Electromechanical modeling; Frequency adaption; Hodgkin–Huxley models; Homogenization; hiPS cardiomyocytes

PMID:
26972766
DOI:
10.1016/j.jbiomech.2016.01.039
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center