Aldosterone downregulates delayed rectifier potassium currents through an angiotensin type 1 receptor-dependent mechanism.

Aldosterone downregulates delayed rectifier potassium currents through an angiotensin type 1 receptor-dependent mechanism. Am J Transl Res. 2018;10(5):1413-1421 Authors: Lv Y, Wang Y, Zhu X, Zhang H Abstract We have previously shown that aldosterone downregulates delayed rectifier potassium currents (IKs) via activation of the mineralocorticoid receptor (MR) in adult guinea pig cardiomyocytes. Here, we investigate whether angiotensin II/angiotensin type 1 receptor (AngII/AT1R) and intracellular calcium also play a role in these effects. Ventricular cardiomyocytes were isolated from adult guinea pigs and incubated with aldosterone (1 μmol·L-1) either alone or in combination with enalapril (1 μmol·L-1), losartan (1 μmol·L-1), nimodipine (1 μmol·L-1), or BAPTA-AM (2.5 μmol·L-1) for 24 h. We used the conventional whole cell patch-clamp technique to record the IKs component. In addition, we evaluated expression of the IKs subunits KCNQ1 and KCNE1 using Western blotting. Our results showed that both enalapril and losartan, but not nimodipine or BAPTA-AM, completely reversed the aldosterone-induced inhibition of IKs and its effects on KCNQ1/KCNE1 protein levels. Furthermore, we found that AngII/AT1R mediates the inhibitory effects of aldosterone on IKs. Finally, the downregulation of IKs induced by aldosterone did not occur secondarily to a change in intracellular calcium concentrations. Taken together, our findings demonstrate th...
Source: American Journal of Translational Research - Category: Research Tags: Am J Transl Res Source Type: research