One-dimensional rabbit sinoatrial node models: Benefits and limitations

被引:61
|
作者
Garny, A
Kohl, P
Hunter, PJ
Boyett, MR
Noble, D
机构
[1] Univ Oxford, Dept Physiol, Oxford OX1 3PT, England
[2] Univ Auckland, Bioengn Inst, Auckland 1, New Zealand
[3] Univ Leeds, Sch Biomed Sci, Leeds LS2 9JT, W Yorkshire, England
关键词
atrium; cardiac excitation; computer model; conduction; electrotonic interaction junctions; pacemaking; rabbit; sinoatrial node;
D O I
10.1046/j.1540.8167.90301.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One-Dimensional Rabbit Sinoatrial Node Models. Introduction: Cardiac multicellular modeling has traditionally focused on ventricular electromechanics. More recently, models of the atria have started to emerge, and there is much interest in addressing sinoatrial node structure and function. Methods and Results: We implemented a variety of one-dimensional sinoatrial models consisting of descriptions of central, transitional, and peripheral sinoatrial node cells, as well as rabbit or human atrial cells. These one-dimensional models were implemented using CMISS on an SGI(R) Origin(R) 2000 supercomputer. Intercellular coupling parameters recorded in experimental studies on sinoatrial node and atrial cell-pairs under-represent the electrotonic interactions that any cardiomyocyte would have in a multidimensional setting. Unsurprisingly, cell-to-cell coupling had to be scaled-up (by a factor of 5) in order to obtain a stable leading pacemaker site in the sinoatrial node center. Further critical parameters include the gradual increase in intercellular coupling from sinoatrial node center to periphery, and the presence of electrotonic interaction with atrial cells. Interestingly, the electrotonic effect of the atrium on sinoatrial node periphery is best described as opposing depolarization, rather than necessarily hyperpolarizing, as often assumed. Conclusion: Multicellular one-dimensional models of sinoatrial node and atrium can provide useful insight into the origin and spread of normal cardiac excitation. They require larger than "physiologic" intercellular conductivities in order to make up for a lack of "anatomical" spatial scaling. Multicellular models for more in-depth quantitative studies will require more realistic anatomico-physiologic properties.
引用
收藏
页码:S121 / S132
页数:12
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