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SKF 12185和SKF 252 A的抗肾上腺皮质活性。

Anti-adrenocortical activity of SKF 12185 and SKF 252 A.

作者信息

Touitou Y, Bogdan A, Legrand J C, Desgrez P

出版信息

Biomedicine. 1976 Jul;25(5):188-90.

PMID:1000030
Abstract

The synthesis of aldosterone and 18-hydroxycorticosterone from triated corticosterone by sheep adrenal homogenate have been studied in presence of increasing concentrations of SKF 12185, a product already known as an inhibitor of cortisol synthesis. An approximately 98% inhibition of the synthesis of both steroids occurred with only 2 x 10(-4) M of the drug. In contrast, incubation of a structurally closely related compound (SKF 252 A) under the same experimental conditions resulted in an only 52% inhibition with higher concentrations (2 x 10(-3) M). These findings could explain the marked aldosterone fall that occurs in SKF 12185 treated subjects and supports the therapeutic use of this product in treatment of hyperaldosteronism.

摘要

在存在浓度不断增加的SKF 12185(一种已知的皮质醇合成抑制剂)的情况下,对绵羊肾上腺匀浆由氚化皮质酮合成醛固酮和18 - 羟皮质酮的过程进行了研究。仅2×10⁻⁴ M的该药物就使两种类固醇的合成受到了约98%的抑制。相比之下,在相同实验条件下,对一种结构密切相关的化合物(SKF 252 A)进行孵育,更高浓度(2×10⁻³ M)时仅导致52%的抑制。这些发现可以解释在接受SKF 12185治疗的受试者中出现的显著醛固酮下降,并支持该产品在原发性醛固酮增多症治疗中的治疗用途。

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