DocumentCode :
3562240
Title :
Simulation study of electrotonic coupling between human atrial myocytes and mechanosensitive fibroblasts
Author :
Honglian Su ; Heqing Zhan ; Yinglan Gong ; Dingchang Zheng ; Ling Xia
Author_Institution :
Dept. of Biomed. Eng., Zhejiang Univ., Hangzhou, China
fYear :
2014
Firstpage :
753
Lastpage :
756
Abstract :
This study aimed to investigate the effect on adjacent myocyte of fibroblasts (Fbs) with the incorporation of mechano-gated currents induced by mechanical compression (lci) of cardiac Fbs. The human atrial myocyte (hAM) was modeled by the Courtemanche-Ramirez-Nattel model. With two different experimentally observed Fbs compression (2 μm and 3 μm), lci was numerically simulated as lcil and lcih. They were then incorporated into two types of electrophysiological models of human atrial Fbs: passive and active models, respectively. In both passive and active models, lci depolarized the membrane potential of cardiac Fbs. When coupled with passive Fbs, the action potential of myocyte duration at 90% (APD90) was increased in comparison with uncoupled hAM. With the incorporation of Ici into passive Fbs, APD90 of myocyte was further increased. When coupled with active Fbs, similar increases were obtained with the incorporation of both lci Furthermore, the resting potential and the maximum value of the action potential of hAM were also increased for both models and with both Ici. The preliminary simulation study confirmed that mechanosentitive currents in fibroblasts play an important role in mechano-electrical coupling.
Keywords :
bioelectric potentials; biomembrane transport; cardiology; mechanoception; muscle; Courtemanche-Ramirez-Nattel model; electrophysiological models; electrotonic coupling; human atrial myocytes; mechanical compression; mechano-gated currents; mechanosensitive fibroblasts; membrane potential; Abstracts; Equations; Fibroblasts; Mathematical model; Mechanical factors; Modeling; Physiology;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Computing in Cardiology Conference (CinC), 2014
ISSN :
2325-8861
Print_ISBN :
978-1-4799-4346-3
Type :
conf
Filename :
7043152
Link To Document :
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