Palem-Vliers M, Fontaine F, Genard P
Endocrinol Exp. 1976 Mar;10(1):59-63.
The affinity of new urinary 18-hydroxy-steroid (Cp x) for mineralocorticoid receptors was estimated. When rat kidney slices were incubated with 2 x 10(-9) M 3H-aldosterone, Cp x (2 x 10(-5) M) was able to compete with aldosterone for the mineralocorticoid cytosol receptors. Cp x had low but significant affinity for mineralocorticoid receptor sites. This affinity was less than that obtained with 18-OH-progesterone. Moreover, in the adrenalectomized rats, the injection of Cp x induced a decrease of urinary Na+/K+ ratio which seems comparable to that obtained with 18-OH-progesterone.
对新型尿18 - 羟基类固醇(Cp x)与盐皮质激素受体的亲和力进行了评估。当用2×10⁻⁹ M的³H - 醛固酮孵育大鼠肾切片时,Cp x(2×10⁻⁵ M)能够与醛固酮竞争盐皮质激素胞浆受体。Cp x对盐皮质激素受体位点具有低但显著的亲和力。这种亲和力低于18 - 羟基孕酮的亲和力。此外,在肾上腺切除的大鼠中,注射Cp x导致尿中Na⁺/K⁺比值下降,这似乎与注射18 - 羟基孕酮所获得的结果相当。