Rate dependency of delayed rectifier currents during the guinea‐pig ventricular action potential

1 The action potential clamp technique was exploited to evaluate the rate dependency of delayed rectifier currents (IKr and IKs) during physiological electrical activity. IKr and IKs were measured in guinea‐pig ventricular myocytes at pacing cycle lengths (CL) of 1000 and 250 ms. 2 A shorter CL, with the attendant changes in action potential shape, was associated with earlier activation and increased magnitude of both IKr and IKs. Nonetheless, the relative contributions of IKr and IKs to total transmembrane current were independent of CL. 3 Shortening of diastolic interval only (constant action potential shape) enhanced IKs, but not IKr. 4 I Kr was increased by a change in the action potential shape only (constant diastolic interval). 5 In ramp clamp experiments, IKr amplitude was directly proportional to repolarization rate at values within the low physiological range (< 1.0 V s−1); at higher repolarization rates proportionality became shallower and finally reversed. 6 When action potential duration (APD) was modulated by constant current injection (I‐clamp), repolarization rates > 1.0 V s−1 were associated with a reduced effect of IKr block on APD. The effect of changes in repolarization rate was independent of CL and occurred in the presence of IKs blockade. 7 In spite of its complexity, the behaviour of IKr was accurately predicted by a numerical model based entirely on known kinetic properties of the current. 8 Both IKr and IKs may be increased at fast heart rates, but this may occur through completely different mechanisms. The mechanisms identified are such as to contribute to abnormal rate dependency of repolarization in prolonged repolarization syndromes.

[1]  E. Wanke,et al.  Disulfide bridges of Ergtoxin, a member of a new sub‐family of peptide blockers of the ether‐a‐go‐go‐related K+ channel , 2000, FEBS letters.

[2]  G. Gintant Characterization and functional consequences of delayed rectifier current transient in ventricular repolarization. , 2000, American journal of physiology. Heart and circulatory physiology.

[3]  E Wanke,et al.  A toxin to nervous, cardiac, and endocrine ERG K+ channels isolated from Centruroides noxius scorpion venom , 1999, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[4]  Arthur J. Moss,et al.  The QT Interval and Torsade de Pointes , 1999, Drug safety.

[5]  J C Hancox,et al.  Alteration of HERG current profile during the cardiac ventricular action potential, following a pore mutation. , 1998, Biochemical and biophysical research communications.

[6]  Harry J. Witchel,et al.  Time course and voltage dependence of expressed HERG current compared with native ”rapid” delayed rectifier K current during the cardiac ventricular action potential , 1998, Pflügers Archiv.

[7]  M. Sanguinetti,et al.  Voltage‐dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits , 1998, The Journal of physiology.

[8]  S Nattel,et al.  Effects of the chromanol 293B, a selective blocker of the slow, component of the delayed rectifier K+ current, on repolarization in human and guinea pig ventricular myocytes. , 1998, Cardiovascular research.

[9]  A. Ferroni,et al.  Dynamic Ca2+-induced inward rectification of K+ current during the ventricular action potential. , 1998, Circulation research.

[10]  S. Nattel,et al.  Effects of the chromanol 293 B , a selective blocker of the slow , component of the delayed rectifier K q current , on repolarization in human and guinea pig ventricular myocytes , 1998 .

[11]  D. Escande,et al.  KvLQT1 potassium channel but not IsK is the molecular target for trans-6-cyano-4-(N-ethylsulfonyl-N-methylamino)-3-hydroxy-2,2-dimethyl- chromane. , 1997, Molecular pharmacology.

[12]  M. Sanguinetti,et al.  Fast inactivation causes rectification of the IKr channel , 1996, The Journal of general physiology.

[13]  S Nattel,et al.  Evidence for two components of delayed rectifier K+ current in human ventricular myocytes. , 1996, Circulation research.

[14]  G. Landes,et al.  Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias , 1996, Nature Genetics.

[15]  S. Priori,et al.  Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy. , 1995, Circulation.

[16]  M. Sanguinetti,et al.  A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel , 1995, Cell.

[17]  E. Green,et al.  A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome , 1995, Cell.

[18]  B. Fermini,et al.  Rapid and slow components of delayed rectifier current in human atrial myocytes. , 1994, Cardiovascular research.

[19]  F. Marumo,et al.  Subcellular mechanism for Ca(2+)-dependent enhancement of delayed rectifier K+ current in isolated membrane patches of guinea pig ventricular myocytes. , 1994, Circulation research.

[20]  M. Sanguinetti,et al.  Rate-dependent prolongation of cardiac action potentials by a methanesulfonanilide class III antiarrhythmic agent. Specific block of rapidly activating delayed rectifier K+ current by dofetilide. , 1993, Circulation research.

[21]  K Shimomura,et al.  Differential Response of QTU Interval to Exercise, Isoproterenol, and Atrial Pacing in Patients with Congenital Long QT Syndrome , 1991, Pacing and clinical electrophysiology : PACE.

[22]  D. Roden,et al.  Time-dependent outward current in guinea pig ventricular myocytes. Gating kinetics of the delayed rectifier , 1990, The Journal of general physiology.

[23]  M. Sanguinetti,et al.  Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents , 1990, The Journal of general physiology.

[24]  M. Kameyama,et al.  Mechanism of receptor‐mediated modulation of the delayed outward potassium current in guinea‐pig ventricular myocytes. , 1990, The Journal of physiology.

[25]  H. Irisawa,et al.  Intracellular Ca2+ and protein kinase C modulate K+ current in guinea pig heart cells. , 1987, The American journal of physiology.