Pro- and antiarrhythmic effects of ATP-sensitive potassium current activation on reentry during early afterdepolarization-mediated arrhythmias.

BACKGROUND Under conditions promoting early afterdepolarizations (EADs), ventricular tissue can become bi-excitable, that is, capable of wave propagation mediated by either the Na current (INa) or the L-type calcium current (ICa,L), raising the possibility that ICa,L-mediated reentry may contribute to polymorphic ventricular tachycardia (PVT) and torsades de pointes. ATP-sensitive K current (IKATP) activation suppresses EADs, but the effects on ICa,L-mediated reentry are unknown. OBJECTIVE To investigate the effects of IKATP activation on ICa,L-mediated reentry. METHODS We performed optical voltage mapping in cultured neonatal rat ventricular myocyte monolayers exposed to BayK8644 and isoproterenol. The effects of pharmacologically activating IKATP with pinacidil were analyzed. RESULTS In 13 monolayers with anatomic ICa,L-mediated reentry around a central obstacle, pinacidil (50 μM) converted ICa,L-mediated reentry to INa-mediated reentry. In 33 monolayers with functional ICa,L-mediated reentry (spiral waves), pinacidil terminated reentry in 17, converted reentry into more complex INa-mediated reentry resembling fibrillation in 12, and had no effect in 4. In simulated 2-dimensional bi-excitable tissue in which ICa,L- and INa-mediated wave fronts coexisted, slow IKATP activation (over minutes) reliably terminated rotors but rapid IKATP activation (over seconds) often converted ICa,L-mediated reentry to INa-mediated reentry resembling fibrillation. CONCLUSIONS IKATP activation can have proarrhythmic effects on EAD-mediated arrhythmias if ICa,L-mediated reentry is present.

[1]  H. Morita,et al.  Early Afterdepolarization Abolished by Potassium Channel Opener in a Patient with Idiopathic Long QT Syndrome , 1995, Journal of cardiovascular electrophysiology.

[2]  D. Roden,et al.  Suppression of repolarization-related arrhythmias in vitro and in vivo by low-dose potassium channel activators. , 1990, Circulation.

[3]  J Jalife,et al.  Optical mapping of drug-induced polymorphic arrhythmias and torsade de pointes in the isolated rabbit heart. , 1997, Journal of the American College of Cardiology.

[4]  Sarah L Vowler,et al.  Making do with what we have: use your bootstraps , 2012, The Journal of physiology.

[5]  Zhilin Qu,et al.  Effects of Na(+) and K(+) channel blockade on vulnerability to and termination of fibrillation in simulated normal cardiac tissue. , 2005, American journal of physiology. Heart and circulatory physiology.

[6]  Y. Aizawa,et al.  Triggers of ventricular tachyarrhythmias and therapeutic effects of nicorandil in canine models of LQT2 and LQT3 syndromes. , 2002, Journal of the American College of Cardiology.

[7]  B. Hoffman,et al.  Antiarrhythmic actions of the ATP-regulated K+ current activated by pinacidil. , 1991, Circulation research.

[8]  N. Yoshimoto,et al.  Nicorandil, a Potassium Channel Opener, Abolished Torsades de Pointes in a Patient with Complete Atrioventricular Block , 1999, Pacing and clinical electrophysiology : PACE.

[9]  Michael J Ackerman,et al.  Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation. , 2010, Circulation.

[10]  Torsade de Pointes , 2003 .

[11]  D. Krikler,et al.  Torsade De Pointes, an atypical ventricular tachycardia. , 1976, British heart journal.

[12]  Z. Qu Critical mass hypothesis revisited: role of dynamical wave stability in spontaneous termination of cardiac fibrillation. , 2006, American journal of physiology. Heart and circulatory physiology.

[13]  Leslie Tung,et al.  IK1 Heterogeneity Affects Genesis and Stability of Spiral Waves in Cardiac Myocyte Monolayers , 2009, Circulation research.

[14]  Alan Garfinkel,et al.  Bi-stable wave propagation and early afterdepolarization-mediated cardiac arrhythmias. , 2012, Heart rhythm.

[15]  A. Garfinkel,et al.  Dynamics of early afterdepolarization-mediated triggered activity in cardiac monolayers. , 2012, Biophysical journal.

[16]  C. Henrikson,et al.  Antiarrhythmic Engineering of Skeletal Myoblasts for Cardiac Transplantation , 2005, Circulation research.

[17]  Guy Salama,et al.  Cytosolic Ca2+ triggers early afterdepolarizations and torsade de pointes in rabbit hearts with type 2 long QT syndrome , 2002, The Journal of physiology.

[18]  F. Riccioppo Neto,et al.  Antiarrhythmic and electrophysiological effects of the novel KATP channel opener, rilmakalim, in rabbit cardiac cells. , 1997, General pharmacology.

[19]  N V Thakor,et al.  Simulation of action potentials from metabolically impaired cardiac myocytes. Role of ATP-sensitive K+ current. , 1996, Circulation research.

[20]  N. Bursac,et al.  Cardiac fibroblast paracrine factors alter impulse conduction and ion channel expression of neonatal rat cardiomyocytes. , 2009, Cardiovascular research.

[21]  Roland N. Emokpae,et al.  Spiral Waves and Reentry Dynamics in an In Vitro Model of the Healed Infarct Border Zone , 2009, Circulation research.

[22]  Ichiro Sakuma,et al.  Mechanisms of destabilization and early termination of spiral wave reentry in the ventricle by a class III antiarrhythmic agent, nifekalant. , 2007, American journal of physiology. Heart and circulatory physiology.

[23]  C. Antzelevitch,et al.  Effects of a K(+) channel opener to reduce transmural dispersion of repolarization and prevent torsade de pointes in LQT1, LQT2, and LQT3 models of the long-QT syndrome. , 2000, Circulation.

[24]  Mya Mya Thu,et al.  Spatially discordant alternans in cardiomyocyte monolayers. , 2008, American journal of physiology. Heart and circulatory physiology.

[25]  Kossmann Ce The long Q-T interval and syndromes. , 1987 .

[26]  L. J. Leon,et al.  Mechanisms of Termination of Atrial Fibrillation by Class I Antiarrhythmic Drugs: , 2003, Journal of cardiovascular electrophysiology.

[27]  Frank B Sachse,et al.  Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[28]  L. Carlsson,et al.  Antiarrhythmic Effects of Potassium Channel Openers in Rhythm Abnormalities Related to Delayed Repolarization , 1992, Circulation.

[29]  J. Vermeulen Mechanisms of Arrhythmias in Heart Failure , 1998, Journal of cardiovascular electrophysiology.

[30]  J. Restrepo,et al.  A rabbit ventricular action potential model replicating cardiac dynamics at rapid heart rates. , 2007, Biophysical journal.