The Effect of Mineralocorticoid Analogues on Na⁺,K⁺-Activated ATPase

Abstract

The effect of 42 steroids of the 20-ketopregnane series with heterocycles fused in positions 16α and 17α on the activity of Na⁺,K⁺-activated ATPase from pig kidney was studied. It was shown that the studied compounds could be divided into two groups. The compounds from the first group stimulate the ATPase at low concentrations (1 × 10^–8–1 × 10^–7 M) and inhibit it at high concentrations (1 × 10^–4 M). The second group of compounds stimulated the sodium pump at either concentration. This is explained by the cooperative action of the ATPase tetramer: after the reaction of its first binding site with the ligand, the tetramer changes the conformation and specificity of its other binding sites. Computer analysis of this series of compounds was carried out and a mathematical model of the dependence of their activities on the structure of their substituents was obtained with a high correlation coefficient and a satisfactory predictive power. This confirmed the structural similarity of the studied compounds with respect to their interaction with the ATPase binding sites. The method of descriptor analysis that was applied in this study is a new variant of approximation; it is based on the use of symbol variables as descriptors.