Cellular Mechanisms of Differential Action Potential Duration Restitution in Canine Ventricular Muscle Cells During Single Versus Double Premature Stimuli

BackgroundWe tested the hypothesis that action potential duration (APD) restitution of normal ventricular muscle cells is different during double premature stimuli (S3) compared with a single premature stimulus (S2). We propose a possible ionic mechanism for such a difference. Methods and ResultsAction potentials and isometric tension were recorded simultaneously from isolated canine right ventricular trabeculae (2×2×10 mm) (n=35). APD and tension restitution curves (APD and peak tension versus diastolic interval [DI]) of S2 and S3 were constructed by the extrastimulus method during pacing at 1,500 msec. The following results were obtained. 1) The APD restitution curve of S2 was different from that of S3. During the restitution of S2, an early biphasic upward hump was present at short DIs. In contrast, a smooth exponential rise was consistently seen during S3 restitution. 2) Peak tension remained significantly (p<0.001) lower during the restitution of S2 than during S3 restitution at all DIs tested. 3) The variation of APD during the initial 100 msec of DI was significantly longer during S3 than S2 (22±5 msec versus 41±5 msec, p<0.001). 4) Caffeine (2 mM, n=5) and ryanodine (10 μM n=5) blocked cyclic variations of tension, presumably by blocking cyclic variations of intracellular calcium ion concentrations ([Ca2+]1), and eliminated the differences in APD restitution between S2 and S3. 5) Nisoldipine at high (5 μM) but not at lower (2 μM n=5) concentration eliminated the differences in restitution of both APD and tension between S2 and S3. 6) BAY K 8644 (100 nM, n=5) had no effect on this difference. ConclusionsGreater variations of APD occur during the restitution of S3 than during S2 at short DIs. These differences appear to be caused by cyclic variations in tension and thus in [Ca2+]1. Calciumsensitive outward currents could explain these differences in APD restitution.

[1]  Kazuzo Kato,et al.  Mechanism of Augmented Premature Responses in Canine Ventricular Muscle , 1979, Circulation research.

[2]  B. R. Jewell,et al.  A study of the factors responsible for rate‐dependent shortening of the action potential in mammalian ventricular muscle. , 1978, The Journal of physiology.

[3]  E. Gang,et al.  Mode of stimulation versus response: validation of a protocol for induction of ventricular tachycardia. , 1985, American heart journal.

[4]  K. Sagawa,et al.  Postextrasystolic Potentiation of the Isolated Canine Left Ventricle: Relationship to Mechanical Restitution , 1985, Circulation research.

[5]  J. C. Bailey,et al.  Action potential duration alternans in dog Purkinje and ventricular muscle fibers. Further evidence in support of two different mechanisms. , 1989, Circulation.

[6]  R. Tsien,et al.  Calcium‐activated transient outward current in calf cardiac Purkinje fibres. , 1980, The Journal of physiology.

[7]  J. Kupersmith,et al.  Activity-dependent extracellular K+ fluctuations in canine Purkinje fibres , 1980, Nature.

[8]  P. Brugada,et al.  Significance of ventricular arrhythmias initiated by programmed ventricular stimulation: the importance of the type of ventricular arrhythmia induced and the number of premature stimuli required. , 1984, Circulation.

[9]  H. Karagueuzian,et al.  The Cellular Electrophysiologic Mechanism of the Dual Actions of Disopyramide on Rabbit Sinus Node Function , 1982, Circulation.

[10]  C. Fisch,et al.  The Relation of Contractile Enhancement to Action Potential Change in Canine Myocardium , 1967, Circulation research.

[11]  G. W. Beeler,et al.  Reconstruction of the action potential of ventricular myocardial fibres , 1977, The Journal of physiology.

[12]  B. Surawicz,et al.  Effects of Antiarrhythmic Drugs on Premature Action Potential Duration in Canine Ventricular Muscle Fibers , 1987, Journal of Cardiovascular Pharmacology.

[13]  W. Karplus,et al.  The simplified-FitzHugh-Nagumo model with action potential duration restitution: effects on 2D wave propagation , 1991 .

[14]  B. Katzung,et al.  Voltage‐clamp studies of transient inward current and mechanical oscillations induced by ouabain in ferret papillary muscle , 1982, The Journal of physiology.

[15]  B. Surawicz,et al.  Effect of antiarrhythmic drugs on the premature action potential duration in canine cardiac Purkinje fibers. , 1985, The Journal of pharmacology and experimental therapeutics.

[16]  W. Karplus,et al.  The Role of Diastolic Outward Current Deactivation Kinetics on the Induction of Spiral Waves , 1991, Pacing and clinical electrophysiology : PACE.

[17]  M. Hiraoka,et al.  Calcium‐sensitive and insensitive transient outward current in rabbit ventricular myocytes. , 1989, The Journal of physiology.

[18]  J. Jalife,et al.  Cardiac Electrophysiology: From Cell to Bedside , 1990 .

[19]  G. Tseng,et al.  Two components of transient outward current in canine ventricular myocytes. , 1989, Circulation research.

[20]  J Jalife,et al.  Supernormal excitability as a mechanism of chaotic dynamics of activation in cardiac Purkinje fibers. , 1990, Circulation research.

[21]  B. G. Bass Restitution of the action potential in cat papillary muscle. , 1975, The American journal of physiology.

[22]  P. Taggart,et al.  Interplay between adrenaline and interbeat interval on ventricular repolarisation in intact heart in vivo. , 1990, Cardiovascular research.

[23]  J. C. Bailey,et al.  Alternans of Action Potential Duration After Abrupt Shortening of Cycle Length: Differences Between Dog Purkinje and Ventricular Muscle Fibers , 1988, Circulation research.

[24]  G. Tseng Calcium Current Restitution in Mammalian Ventricular Myocytes is Modulated by Intracellular Calcium , 1988, Circulation research.

[25]  M. Lab,et al.  Changes in intracellular calcium during mechanical alternans in isolated ferret ventricular muscle. , 1990, Circulation research.

[26]  W. Wier,et al.  Intracellular calcium transients underlying the short‐term force‐interval relationship in ferret ventricular myocardium. , 1986, The Journal of physiology.

[27]  N. El-Sherif,et al.  Reentrant ventricular arrhythmias in the late myocardial infarction period in the dog. 13. Correlation of activation and refractory maps. , 1985, Circulation research.

[28]  James B. Bassingthwaighte,et al.  Relationship between internal calcium and outward current in mammalian ventricular muscle; a mechanism for the control of the action potential duration? , 1976, The Journal of physiology.

[29]  M. Franz,et al.  Cycle length dependence of human action potential duration in vivo. Effects of single extrastimuli, sudden sustained rate acceleration and deceleration, and different steady-state frequencies. , 1988, The Journal of clinical investigation.

[30]  M. Hiraoka,et al.  Mechanism of increased amplitude and duration of the plateau with sudden shortening of diastolic intervals in rabbit ventricular cells. , 1987, Circulation research.

[31]  D. Noble,et al.  The interpretation of the T wave of the electrocardiogram. , 1978, Cardiovascular research.

[32]  C. Cohen,et al.  A Dihydropyridine (Bay k 8644) That Enhances Calcium Currents in Guinea Pig and Calf Myocardial Cells: A New Type of Positive Inotropic Agent , 1985, Circulation Research.

[33]  R. Kass Nisoldipine: a new, more selective calcium current blocker in cardiac Purkinje fibers. , 1982, The Journal of pharmacology and experimental therapeutics.

[34]  B. Surawicz,et al.  Characteristics and Possible Mechanism of Ventricular Arrhythmia Dependent on the Dispersion of Action Potential Durations , 1983, Circulation.

[35]  H. Karagueuzian,et al.  Increased Temporo‐Spatial Dispersion of Repolarization During Double Premature Stimulation in the Intact Ventricle , 1992, Pacing and clinical electrophysiology : PACE.

[36]  B. Surawicz,et al.  Cycle length effect on restitution of action potential duration in dog cardiac fibers. , 1983, The American journal of physiology.

[37]  J M de Bakker,et al.  Reentry as a cause of ventricular tachycardia in patients with chronic ischemic heart disease: electrophysiologic and anatomic correlation. , 1988, Circulation.