Page 103 - Cardiac Electrophysiology | A Modeling and Imaging Approach
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        Figure 3.20. Ring-shaped fiber model,
        consisting of up to 1500 cells. A primary
        stimulus was applied at the top of the
        ring (cell 1) and a premature stimulus
        at cell 3 during the relative refractory
        period of the primary AP. Solid arrows
        inside the ring represent propagation
        of the premature (reentrant) AP. It blocks
        in the antegrade direction (=symbol)
        and reenters in the retrograde direction.
        Dashed arrows outside the ring
        represent propagation of the primary
        AP. Due to symmetry, it collides and
        blocks at the bottom cell of the ring.
        From Quan and Rudy [222], with
        permission from Wolters Kluwer
        Health, Inc.









        decreases, cycle length and action potential duration decrease; for 600 cells action potential
        duration is 245 msec, while for 100 cells it is only 60 msec. For both rings the action potential
        duration is constant and reentry is stable. For medium size rings between these two extremes
        (length~λ), action potential duration oscillates dynamically from beat to beat. The amplitude of
        these beat-to-beat oscillations (alternans) is maximum at a ring size of 350 cells and decreases in

        either direction (decrease or increase in ring size). This is seen clearly in Figure 3.21B, where
        action potential duration from different size rings is shown as a function of the corresponding
        cycle length. The upper curve (solid symbols) corresponds to the long action potential and the

        bottom curve (open symbols) to the short action potential of consecutive beats.  Inspection of the
        underlying ionic currents (not shown) clarifies that alternating kinetics of I  (incomplete deactiva-
                                                                                          Ks
        tion after the long action potential and complete deactivation following the short action potential)
        is the major mechanism of action potential duration alternans, with additional contribution from
        I   . Note that for ring size of 50 cells reentry is not sustained.
         Ca,L

               For sufficiently small rings, sodium channels which determine conduction velocity, do
        not recover completely from inactivation between beats and their availability alternates. Conse-

        quently, cycle length oscillations appear together with oscillations of action potential duration
        (Figure 3.22A).  238  Note that the amplitude of cycle length oscillations is smaller than that of the
        action potential duration at any point of the reentrant pathway, as observed experimentally. When
        plotted spatially along the pathway (Figure 3.22B), cycle length and action potential duration are
        not constant during one cycle. These spatial variations are functional in nature, as the ring is

        intrinsically homogeneous. This behavior implies that concepts such as the wavelength of
        excitation are location dependent; for the entire reentry pathway they can only be defined in an
        average sense. More recent simulations,     239  over long time periods, revealed more complex patterns
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