Vol. 288, Issue 2, 858-865, February 1999

Block of Potassium Currents in Guinea Pig Ventricular Myocytes and Lengthening of Cardiac Repolarization in Man by the Histamine H1 Receptor Antagonist Diphenhydramine¹

Majed Khalifa, Benoit Drolet, Pascal Daleau, Christophe Lefez, Marcel Gilbert, Sylvain Plante, Gilles E. O'Hara, Onil Gleeton, Bettina A. Hamelin and Jacques Turgeon

Quebec Heart Institute, Laval Hospital, Faculty of Pharmacy, Laval University (M.K., B.D., B.A.H., J.T.), and Faculty of Medicine, Laval University (P.D., M.G., J.T.), Sainte-Foy, PQ, Canada

Treatment with second generation histamine H1 receptor antagonists has been associated with lengthening of the Q-T interval and proarrhythmia. Similarly, lengthening of the Q-T interval has been reported in patients after overdosing with diphenhydramine (DPH), a first generation agent. Therefore, our study was designed 1) to assess effects of DPH on cardiac repolarization and 2) to characterize effects of the drug on major voltage-dependent cardiac K⁺ currents. First, we noticed that oral administration of DPH at usual dosages to healthy volunteers or to patients (prior to angioplasty) was associated with prolongation of the Q-T_c interval. Although this effect was modest in most individuals, Q-T_c was increased more than 20 ms in 7 of 20 patients. Second, we noticed that exposure of isolated guinea pig hearts to DPH 10⁵ M caused a lengthening of monophasic action potential duration. This effect was potentiated by the combined perfusion of other K⁺ channel blockers such as indapamide. Finally, experiments performed with the patch-clamp technique demonstrated unequivocal block of the rapid component of the delayed rectifier (I_Kr) by DPH; however, IC₅₀ determined for block of I_Kr (3 · 10⁵ M) is ~40-fold greater than plasma concentrations of the drug measured at usual dosages (7 · 10⁷ M). Consequently, in agreement with the long-term clinical use of the drug, prolongation of cardiac repolarization should be minimal in most patients at usual dosages but may be observed with overdosing. Nevertheless, caution remains since excessive lengthening of cardiac repolarization may occur after administration of DPH with other drugs due to 1) concomitant block of other ionic currents or 2) pharmacokinetic interactions leading to toxic concentrations of DPH.