Short- and Long-Term Effects of Amiodarone on the Two Components of Cardiac Delayed Rectifier K + Current

Abstract

Background —Amiodarone is the most promising drug for the treatment of life-threatening tachyarrhythmias in patients with structural heart disease. The pharmacological effects of amiodarone on cardiac ion channels are complex and may differ for short-term and long-term administration. Methods and Results —The delayed rectifier K + current (I K ) of ventricular myocytes isolated from rabbit hearts was recorded with the whole-cell voltage-clamp technique. I K was separated into 2 components by use of specific blockers for either I Ks (chromanol 293B, 30 μmol/L) or I Kr (E-4031, 10 μmol/L). Short-term application of amiodarone caused a concentration-dependent decrease in I Kr with an IC 50 of 2.8 μmol/L (n=8) but only a minimal reduction in I Ks . The short-term effects of amiodarone were also determined in Xenopus oocytes expressing the cloned human channels that conduct I Kr and I Ks (HERG and KvLQT1/minK). HERG current in oocytes was reduced by amiodarone (IC 50 =38 μmol/L), whereas KvLQT1/minK current was unaffected by 300 μmol/L amiodarone. To study the effects of long-term drug administration, rabbits were treated for 4 weeks with oral amiodarone (100 mg · kg −1 · d −1 ) before cell isolation. Long-term administration of amiodarone decreased I K to 55% (n=10) in control rabbits and altered the relative density of I Kr and I Ks . The majority (92%) of current was I Kr . mRNA levels of rabbit ERG , KVLQT1 , and minK in left ventricular myocardium did not differ between control and long-term amiodarone. Conclusions —Amiodarone has differential effects on the 2 components of I K , depending on the application period; short-term treatment inhibits primarily I Kr , whereas long-term treatment reduces I Ks .