Publication | Open Access
Effects of diltiazem and nifedipine on transient outward and ultra‐rapid delayed rectifier potassium currents in human atrial myocytes
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Citations
26
References
2005
Year
Cardiac MuscleCardiovascular PharmacologyPharmacotherapyCellular PhysiologySocial SciencesMolecular PharmacologyHyperpolarization (Biology)Rectifier Potassium CurrentsRepolarization KCardiologyTransient OutwardIon ChannelsChannel BlockersPharmacologyPotassium HomeostasisNeurophysiologyHuman AtriumPhysiologyElectrophysiologyCardiovascular PhysiologyMedicineHuman Atrial Myocytes
1. It is unknown whether the widely used L-type Ca(2+) channel antagonists diltiazem and nifedipine would block the repolarization K(+) currents, transient outward current (I(to1)) and ultra-rapid delayed rectifier K(+) current (I(Kur)), in human atrium. The present study was to determine the effects of diltiazem and nifedipine on I(to1) and I(Kur) in human atrial myocytes with whole-cell patch-clamp technique. 2. It was found that diltiazem substantially inhibited I(to1) in a concentration-dependent manner, with an IC(50) of 29.2+/-2.4 microM, and nifedipine showed a similar effect (IC(50)=26.8+/-2.1 muM). The two drugs had no effect on voltage-dependent kinetics of the current; however, they accelerated I(to1) inactivation significantly, suggesting an open channel block. 3. In addition, diltiazem and nifedipine suppressed I(Kur) in a concentration-dependent manner (at +50 mV, IC(50)=11.2+/-0.9 and 8.2+/-0.8 microM, respectively). These results indicate that the Ca(2+) channel blockers diltiazem and nifedipine substantially inhibit I(to1) and I(Kur) in human atrial myocytes.
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