Multi-scale virtual human ventricle

SZ Shugang Zhang
WL Weigang Lu
FY Fei Yang
ZL Zhen Li
SW Shuang Wang
MJ Mingjian Jiang
XW Xiaofeng Wang
ZW Zhiqiang Wei
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The propagation of excitation waves was described using the monodomain equation43,

where D is the diffusion coefficient tensor for describing the intercellular electrical coupling via gap junctions.

For one-dimensional (1D) simulations, a 15 mm long transmural 1D strand of 100 nodes with spacing 0.15 mm was constructed. The strand length was consistent with the normal range of human transmural ventricle width (4–14 mm) in previous studies61,62. The ratio of ENDO:MCELL:EPI was set to 37:26:37 as in previous study14. The diffusion coefficient was set to 0.154 mm2/ms to get a conduction velocity of 71.9 cm/s, which was very close to the 70 cm/s that recorded in the human myocardium63.

The 1D strand was expanded in the y direction to form a 15 × 60 mm2 two-dimensional (2D) tissue sheet. Isotropic cell-to-cell coupling was assumed in the idealized model, and the isotropic coefficient was kept the same as in the 1D strand. For the realistic 2D ventricle tissue slice, the D was anisotropic and the coefficients along and perpendicular to the fiber orientation were set to 0.154 and 0.0385 mm2/ms, respectively. For the realistic three-dimensional (3D) bi-ventricle geometry, the anisotropic coefficients were the same as in the 2D realistic tissue slice. The anatomical geometries of realistic 2D ventricular slice and 3D ventricle were reconstructed from DT-MRI64,65.

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