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

Article

关键词: POTASSIUM CHANNEL;    DEPENDENT BLOCK;    HEART;    REPERFUSION;    ANTAGONISTS;    RECEPTORS;   

DOI  :  10.1161/01.CIR.101.10.1199

来源: SCIE

【 摘 要 】

Background-The effects of type 1 angiotensin II receptor antagonist losartan 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 myocytes 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 being 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 myocytes, losartan and,E3174 inhibited the I-Ks (18.4 +/- 3.2% and 6.5 +/- 0.7%, respectively). 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 90% of repolarization, whereas E3174 slowed only the final phase of the repolarization process. Conclusions-These results demonstrated that at therapeutic concentrations, both losartan and E3174 modified the cardiac delayed rectifier hKv1.5, HERG, and Ks currents.

【 授权许可】

Free