Literature DB >> 3708767

Dynamic interactions and mutual synchronization of sinoatrial node pacemaker cells. A mathematical model.

D C Michaels, E P Matyas, J Jalife.   

Abstract

Dynamic interactions and mutual entrainment of coupled sinoatrial pacemaker cells with different intrinsic frequencies were investigated using a computerized mathematical model. Transmembrane potentials were simulated using equations of individual membrane currents based on voltage clamp data for the sinoatrial node. The intrinsic frequency of a given cell was altered by applying bias hyperpolarizing current, or by changing the amount of slow inward current. Cells were coupled through simple ohmic resistances to form linear arrays of two or more cells. Simulations closely reproduced previous experimental work showing that the mutual interactions between pacemakers are mediated electrotonically and show phase dependence. Results from the present simulations provide an explanation for the ionic basis of these phase-dependent interactions. In addition, it is demonstrated that the mutual entrainment of coupled pacemakers can lead to their coordinated behavior (synchronization). Two pacemaker cells can synchronize at simple harmonic (i.e., 1:1, 2:1, etc.) or more complex ratios (3:2, 5:3, etc.), depending on the differences in intrinsic frequencies and the degree of electrical coupling between cells. Simulations using larger numbers of linearly connected cells yielded various patterns of pacemaker activity including 2:1 sinoatrial block and complex dysrhythmic activity. The overall results may be used to predict higher order interactions of thousands of cells comprising the sinus node. Under such a scheme, synchronization occurs not by the conducted influence of a dominant pacemaker cell, but by the mutual "democratic" interaction of individual pacemaker cells.

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Year:  1986        PMID: 3708767     DOI: 10.1161/01.res.58.5.706

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  19 in total

1.  Phase response curve based model of the SA node: simulation by two-dimensional array of pacemaker cells with randomly distributed cycle lengths.

Authors:  S Abramovich-Sivan; S Akselrod
Journal:  Med Biol Eng Comput       Date:  1999-07       Impact factor: 2.602

2.  Multiple oscillators provide metastability in rhythm generation.

Authors:  H S Chang; K Staras; M P Gilbey
Journal:  J Neurosci       Date:  2000-07-01       Impact factor: 6.167

Review 3.  Does the atrioventricular node conduct?

Authors:  F L Meijler; C Fisch
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4.  Model for synchronization of pancreatic beta-cells by gap junction coupling.

Authors:  A Sherman; J Rinzel
Journal:  Biophys J       Date:  1991-03       Impact factor: 4.033

5.  The relevance of non-excitable cells for cardiac pacemaker function.

Authors:  John P Fahrenbach; Rafael Mejia-Alvarez; Kathrin Banach
Journal:  J Physiol       Date:  2007-10-11       Impact factor: 5.182

6.  Cardiac arrhythmias modelled by Cai-inactivated Ca2+ channels.

Authors:  M H Lambert; T R Chay
Journal:  Biol Cybern       Date:  1989       Impact factor: 2.086

7.  Synchronization of sinoatrial node pacemaker cell clocks and its autonomic modulation impart complexity to heart beating intervals.

Authors:  Yael Yaniv; Ismayil Ahmet; Jie Liu; Alexey E Lyashkov; Toni-Rose Guiriba; Yosuke Okamoto; Bruce D Ziman; Edward G Lakatta
Journal:  Heart Rhythm       Date:  2014-04-05       Impact factor: 6.343

8.  Pacemaker synchronization of electrically coupled rabbit sinoatrial node cells.

Authors:  E E Verheijck; R Wilders; R W Joyner; D A Golod; R Kumar; H J Jongsma; L N Bouman; A C van Ginneken
Journal:  J Gen Physiol       Date:  1998-01       Impact factor: 4.086

9.  Initiation and entrainment of multicellular automaticity via diffusion limited extracellular domains.

Authors:  Steven Poelzing; Seth H Weinberg; James P Keener
Journal:  Biophys J       Date:  2021-10-30       Impact factor: 4.033

10.  Decreased intercellular coupling improves the function of cardiac pacemakers derived from mouse embryonic stem cells.

Authors:  John P Fahrenbach; Xun Ai; Kathrin Banach
Journal:  J Mol Cell Cardiol       Date:  2008-09-11       Impact factor: 5.000

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