Propagation on a central fiber surrounded by inactive fibers in a multifibered bundle model.

We studied uniform propagation on a central active fiber surrounded by inactive fibers in a multifibered bundle model lying in a large volume conductor. The behavior of a fully active bundle is considered in a companion paper. The bundle is formed by concentric layers of small cylindrical fibers (radius 5 microns), with a uniform minimum distance (d) between any two adjacent fibers, to yield a bundle radius of about 72 microns. Individual fibers are identical continuous cables of excitable membrane based on a modified Beeler-Reuter model. The intracellular volume fraction (fi) increases to a maximum of about 90% as d is reduced and remains unchanged for d < 0.01 micron. In the range of d < 0.01 micron, the central fiber is effectively shielded from external effects by the first concentric layer of inactive fibers, and a large capacitive load current flows across the surrounding inactive membranes. In addition, the fiber proximity produces a circumferentially nonuniform current density (proximity effect) that is equivalent to an increased average longitudinal interstitial resistance. The conduction velocity is reduced as d becomes smaller in the range of d < 0.1 micron, the interstitial potential becomes larger, and both the maximum rate of rise and time constant of the foot of the upstroke are increased. On the other hand, for d > 0.1 micron, there are negligible changes in the shape of the upstroke, and the behavior of the central fiber is close to that of a uniform cable in a restricted volume conductor. For d larger than about 1.2 microns, the active fiber environment is close to an unbounded isotropic volume conductor.

A model study of electric field interactions between cardiac myocytes.

The transmission of excitation via electric field coupling was studied in a model comprising two myocytes abutted end-to-end and placed in an unbounded volume conductor. Each myocyte was modeled as a small cylinder of membrane (10 microns in diameter and 100 microns in length) capped at both ends. A Beeler-Reuter model modified for the Na+ current dynamics served to simulate the membrane ionic current. There was no resistive coupling between the myocytes and the intercellular junction consisted of closely apposed pre- and post-junctional membranes, separated by a uniform cleft distance. The membrane current crossing the prejunctional membrane during the action potential upstroke tends to flow out of the cleft, but it is partly prevented from doing so by the shunt resistance constituted by the cleft volume conductor. The prejunctional upstroke gives rise to a pulse of positive potential within the cleft which induces a small capacitive current across the post-junctional membrane to yield a small positive change in the intracellular potential in the post-junctional cell. The net result is an hyperpolarization of the post-junctional cleft membrane and a slight depolarization of the rest of the cell membrane since the extracellular potential outside of the cell is zero. The magnitude of this depolarization is quite small for a flat junctional membrane and it can be increased by membrane folding and interdigitation, so as to increase the junctional membrane area by a factor of 10 or more. Even then the post-junctional depolarization does not reach threshold when the extracellular potential around the post-junctional cell is effectively zero. Threshold depolarization occurs in the presence of a large decrease of post-junctional load, by increasing the junctional membrane capacitance and/or decreasing the volume of the post-junctional cell. Assuming that the normal resistive coupling between two cardiac myocytes is 1-4 M omega, our model study indicates that electric field coupling would then be about two orders of magnitude smaller. However, substantial enhancement of the efficacy of electric field transmission was observed in the case of cells with substantial junctional membrane folding.