Regulation of potassium channels by nonsedating antihistamines.

BACKGROUND Terfenadine and astemizole are widely prescribed nonsedating antihistamines that have been associated with QT-interval prolongation and ventricular arrhythmias. Since potassium channels are intrinsically involved in repolarization, this study was designed to evaluate the effect of the nonsedating antihistamines on potassium channel modulation. METHODS AND RESULTS The whole-cell patch-clamp technique was used to study K+ currents in enzymatically isolated rat and guinea pig ventricular myocytes. Three distinct K+ channels were examined: the inward rectifier (IK1), the delayed rectifier (IK), and the transient outward (I(to)) currents. The dialyzing pipette solution was buffered with EGTA, and ionic channels other than potassium were pharmacologically inhibited or electrically inactivated. Both astemizole and terfenadine suppressed the IK1 channel by 17% to 50% in a voltage-dependent manner in rat and guinea pig myocytes. Ito was evaluated in rat ventricular myocytes. Both drugs also inhibited the maintained component of I(to) to a lesser extent, by 23%, in a dose-dependent, reversible manner. IK was examined mainly in guinea pig myocytes. Terfenadine but not astemizole slightly inhibited IK, by 9%, and only at higher drug concentrations. The medications had dose-dependent inhibitory actions, with specific K+ channel suppression evident only beginning at concentrations > 0.1 mumol/L. CONCLUSIONS These findings suggest that the mechanism of action of the rare proarrhythmic effects of the nonsedating antihistamines appears to be secondary to potassium channel blockade. A significant voltage-dependent blockade of the IK1 channel was demonstrated, as well as additional inhibitory effects on I(to) and IK channels. These actions lead to delayed repolarization, QT interval prolongation, and enhanced susceptibility to the development of premature ventricular depolarizations. Caution is advised in the prescription of nonsedating antihistamines, particularly in patients at risk of elevated serum levels of the antihistamine or patients with existing repolarization abnormalities.

[1]  F. Simons,et al.  The pharmacology and use of H1-receptor-antagonist drugs. , 1994, The New England journal of medicine.

[2]  A. Brown,et al.  Effects of terfenadine and its metabolites on a delayed rectifier K+ channel cloned from human heart. , 1993, Molecular pharmacology.

[3]  Y Chen,et al.  Mechanism of the cardiotoxic actions of terfenadine. , 1993, JAMA.

[4]  D. Wortham,et al.  Terfenadine-ketoconazole interaction. Pharmacokinetic and electrocardiographic consequences. , 1993, JAMA.

[5]  P. Dowd,et al.  The new H1 antihistamines. Treatment of urticaria and other clinical problems. , 1993, Dermatologic clinics.

[6]  Antihistamines--is there anything safe to prescribe? , 1992 .

[7]  R. Woosley,et al.  Changes in the pharmacokinetics and electrocardiographic pharmacodynamics of terfenadine with concomitant administration of erythromycin , 1992, Clinical pharmacology and therapeutics.

[8]  E. Carmeliet Voltage- and time-dependent block of the delayed K+ current in cardiac myocytes by dofetilide. , 1992, The Journal of pharmacology and experimental therapeutics.

[9]  C. Wiley,et al.  Cardiotoxic effects of astemizole overdose in children. , 1992, The Journal of pediatrics.

[10]  K. Chinn,et al.  Contribution of delayed rectifier and inward rectifier to repolarization of the action potential: pharmacologic separation. , 1992, Journal of cardiovascular pharmacology.

[11]  R. Myerburg,et al.  Potassium rectifier currents differ in myocytes of endocardial and epicardial origin. , 1992, Circulation research.

[12]  R. Kass,et al.  Distinct voltage-dependent regulation of a heart-delayed IK by protein kinases A and C. , 1991, The American journal of physiology.

[13]  G. Morley,et al.  Dynamics of the inward rectifier K+ current during the action potential of guinea pig ventricular myocytes. , 1991, Biophysical journal.

[14]  J. Brenner,et al.  Astemizole-induced cardiac conduction disturbances in a child. , 1991, JAMA.

[15]  K. Kouvalainen,et al.  Accidental astemizole overdose in young children , 1991, The Lancet.

[16]  J. Leor,et al.  Giant U waves and associated ventricular tachycardia complicating astemizole overdose: successful therapy with intravenous magnesium. , 1991, The American journal of medicine.

[17]  M. Morad,et al.  The transient K+ current in rat ventricular myocytes: evaluation of its Ca2+ and Na+ dependence. , 1991, The Journal of physiology.

[18]  C. L. Ferguson,et al.  Torsades de pointes occurring in association with terfenadine use. , 1990, JAMA.

[19]  H. Nakaya,et al.  Effects of N-acetylprocainamide and sotalol on ion currents in isolated guinea-pig ventricular myocytes. , 1990, European journal of pharmacology.

[20]  S. Nattel,et al.  Erythromycin-induced long QT syndrome: concordance with quinidine and underlying cellular electrophysiologic mechanism. , 1990, The American journal of medicine.

[21]  M. Morad,et al.  Tedisamil blocks the transient and delayed rectifier K+ currents in mammalian cardiac and glial cells. , 1990, The Journal of pharmacology and experimental therapeutics.

[22]  T. Colatsky,et al.  Block of delayed rectifier potassium current, IK, by flecainide and E-4031 in cat ventricular myocytes. , 1990, Circulation.

[23]  L. DeFelice,et al.  Potassium Channels and the Repolarization of Cardiac Cells a , 1990, Annals of the New York Academy of Sciences.

[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]  J. Crowe,et al.  Nonsedating histamine H1-receptor antagonists. , 1989, Clinical pharmacy.

[26]  T. Begenisich,et al.  Beta-adrenergic modulation of cardiac ion channels. Differential temperature sensitivity of potassium and calcium currents , 1989, The Journal of general physiology.

[27]  P. Gaudry,et al.  Prolonged Q-T interval following astemizole overdose. , 1989, Archives of emergency medicine.

[28]  V. Harindra,et al.  Cardiotoxic effect with convulsions in terfenadine overdose. , 1989, BMJ.

[29]  W. Giles,et al.  Comparison of potassium currents in rabbit atrial and ventricular cells. , 1988, The Journal of physiology.

[30]  A. Pelech,et al.  ASTEMIZOLE-INDUCED TORSADE DE POINTES , 1988, The Lancet.

[31]  J. Watkins,et al.  TOR-SADES DE POINTES VENTRICULAR TACHYCARDIA ASSOCIATED WITH ASTE-MIZOLE OVERDOSE , 1988 .

[32]  R. Harvey,et al.  Characterization of the inward-rectifying potassium current in cat ventricular myocytes , 1988, The Journal of general physiology.

[33]  D. Escande,et al.  Two types of transient outward currents in adult human atrial cells. , 1987, The American journal of physiology.

[34]  T M Craft,et al.  Torsade de pointes after astemizole overdose. , 1986, British medical journal.

[35]  A. Wolff,et al.  Histamine and cardiac arrhythmias. , 1986, Circulation research.

[36]  J. Hume,et al.  Ionic basis of the different action potential configurations of single guinea‐pig atrial and ventricular myocytes. , 1985, The Journal of physiology.

[37]  J. Spear,et al.  Cesium chloride-induced long QT syndrome: demonstration of afterdepolarizations and triggered activity in vivo. , 1985, Circulation.

[38]  A. Brown,et al.  Early Outward Current in Rat Single Ventricular Cells , 1984, Circulation research.

[39]  J. McNeill,et al.  Cardiac histamine receptors: differences between left and right atria and right ventricle. , 1977, The Journal of pharmacology and experimental therapeutics.