Kafer C J
Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
Comput Biomed Res. 1991 Dec;24(6):549-63. doi: 10.1016/0010-4809(91)90039-y.
An electrophysical/anatomical computer model of human atrial excitation was used to investigate the controversy over specialized internodal pathways. The only atrial pathways that have been thoroughly described in the literature are those that connect the sinoatrial (SA) and atrioventricular (AV) nodes, and the right and left atria. By incorporating pathways of rapid propagation representing the internodal and interatrial tracts, anisotropy was introduced into an otherwise isotropic atrial model. Simulated epicardial isochrone maps, heart vector loops, and electrograms were calculated for both the isotropic and anisotropic atrial models, and the simulations were compared with observed normal data. Although the simulations using the anisotropic model compare more favorably with real data, the results suggest that there are more pathways of rapid propagation in the atria than those described and that a global anisotropy based on morphology and fiber direction is a more likely explanation than rapid propagation confined to a few specialized pathways.
利用人类心房兴奋的电生理/解剖学计算机模型来研究关于特殊结间通路的争议。文献中详尽描述的唯一心房通路是连接窦房(SA)结和房室(AV)结以及左右心房的通路。通过纳入代表结间和房间束的快速传播通路,将各向异性引入原本各向同性的心房模型。针对各向同性和各向异性心房模型计算模拟的心外膜等时线图、心脏向量环和心电图,并将模拟结果与观察到的正常数据进行比较。尽管使用各向异性模型的模拟结果与实际数据的比较更为理想,但结果表明心房中快速传播的通路比所描述的更多,并且基于形态和纤维方向的整体各向异性比局限于少数特殊通路的快速传播更有可能是其原因。