DocumentCode
3375079
Title
Computational study of the relative contribution of channel and gap junction remodelling on human atrial conduction during fibrillation
Author
Zhang, H. ; Zhu, J.J. ; Garratt, C.J. ; Holden, A.V.
Author_Institution
Manchester Univ., UK
fYear
2004
fDate
19-22 Sept. 2004
Firstpage
141
Lastpage
144
Abstract
Chronic atrial fibrillation (AF) induces remodelling of both channel conductance and intercellular coupling in the human atrium. Effects of these changes and their relative contributions to atrial impulse conduction during fibrillation are unknown. In this study we constructed a virtual human atrial strand by incorporating the Nygren et al model of human atrial action potential into a 1-dimensional reaction diffusion partial differential equation. Experimental data on AF-induced changes of human atrial ionic channel conductances and kinetics and gap junction coupling were incorporated into a model to investigate their contributions and relative importance on conduction velocity (CV) at different rates. At low rates (stimulus interval SI>270 ms), AF-induced channel or gap junction remodelling reduced CV significantly. At high rates (SI<270 ms), channel remodelling increased CV while gap junction remodelling reduced the CV. When combined, channel and gap junction remodelling reduced CV additively. Spatial heterogeneities in gap junction coupling can produce intermittent conduction block.
Keywords
bioelectric potentials; biomembrane transport; blood vessels; cardiovascular system; diseases; partial differential equations; reaction-diffusion systems; 1-dimensional reaction diffusion; channel conductance; channel remodelling; chronic atrial fibrillation; computational study; conduction velocity; gap junction remodelling; human atrial action potential model; human atrial impulse conduction; intercellular coupling; intermittent conduction block; partial differential equation; spatial heterogeneities; virtual human atrial strand; Anatomical structure; Animals; Atrial fibrillation; Augmented virtuality; Biomembranes; Humans; Indium phosphide; Instruments; Kinetic theory; Proteins;
fLanguage
English
Publisher
ieee
Conference_Titel
Computers in Cardiology, 2004
Print_ISBN
0-7803-8927-1
Type
conf
DOI
10.1109/CIC.2004.1442891
Filename
1442891
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