Losartan and its metabolite E3174 modify cardiac delayed rectifier K+ currents

Background-The effects of type 1 angiotensin II receptor antagonist losarta n and its metabolite E3174 on transmembrane action potentials, hKv1.5, HERG , and I-Ks currents were analyzed. Methods and Results-Guinea pig ventricular action potentials were recorded with microelectrode techniques and hKv1.5 and HERG currents with the whole- cell patch-clamp technique. I-Ks was recorded in guinea pig ventricular myo cytes with the perforated-nystatin-patch configuration. Losartan and E3174 transiently increased the hKv1.5 current by 8.0 +/- 1.4% and 7.4 +/- 1.6%, respectively. Thereafter, they produced a voltage-dependent block, E3174 be ing more potent than losartan (P<0.05) for this effect. Losartan decreased HERG currents elicited at 0 mV (23.3 +/- 4.8%), whereas E3174 increased the current (30.5 +/- 6.2%). Both drugs shifted the midpoint of the activation curve of HERG channels to more negative potentials. In ventricular myocyte s, losartan and,E3174 inhibited the I-Ks (18.4 +/- 3.2% and 6.5 +/- 0.7%, r espectively). Losartan-induced block was voltage-independent, whereas E3174 shifted the midpoint of the activation curve to more negative potentials. Losartan lengthened the duration of the action potentials at both 50% and 9 0% of repolarization, whereas E3174 slowed only the final phase of the repo larization process. Conclusions-These results demonstrated that at therapeutic concentrations, both losartan and E3174 modified the cardiac delayed rectifier hKv1.5, HERG , and Ks currents.