Panesar N S, Herries D G, Stitch S R
J Endocrinol. 1979 Feb;80(2):229-38. doi: 10.1677/joe.0.0800229.
Male Wistar rats were treated for three weeks with cyproterone (1.7 or 5.1 mg/day) or cyproterone acetate (2 or 6 mg/day). The adrenal weights of animals treated with either dose of cyproterone acetate were significantly less (P less than 0.001) than those of untreated animals. In contrast, the adrenal weights of animals treated with cyproterone did not differ from those of the controls. The concentrations of corticosterone in the plasma were significantly less (P less than 0.001) in both groups treated with cyproterone acetate compared with those of the controls; only the higher dose of cyproterone reduced the plasma concentration of corticosterone (P less than 0.001). Cyproterone acetate inhibited the rat adrenal 3beta-hydroxysteroid dehydrogenase-5-ene,4-ene-isomerase complex in vitro, with both pregnenolone and dehydroepiandrosterone as substrates. Analysis of the reaction rates suggested an uncompetitive mode of inhibition. These results suggest that in rats the antiandrogens cyproterone and cyproterone acetate may provoke adrenal insufficiency by inhibition of steroid biosynthesis. Furthermore, indirect evidence from the mass and morphology of the adrenal suggests that cyproterone acetate may also suppress production or secretion of ACTH by the pituitary gland.
雄性Wistar大鼠用环丙孕酮(1.7或5.1毫克/天)或醋酸环丙孕酮(2或6毫克/天)治疗三周。用任何一种剂量的醋酸环丙孕酮治疗的动物的肾上腺重量均显著低于未治疗动物(P小于0.001)。相比之下,用环丙孕酮治疗的动物的肾上腺重量与对照组无差异。与对照组相比,用醋酸环丙孕酮治疗的两组动物血浆中皮质酮的浓度均显著降低(P小于0.001);只有较高剂量的环丙孕酮降低了血浆皮质酮浓度(P小于0.001)。醋酸环丙孕酮在体外抑制大鼠肾上腺3β-羟基类固醇脱氢酶-5-烯,4-烯-异构酶复合物,以孕烯醇酮和脱氢表雄酮作为底物。反应速率分析表明为非竞争性抑制模式。这些结果表明,在大鼠中,抗雄激素环丙孕酮和醋酸环丙孕酮可能通过抑制类固醇生物合成而引发肾上腺功能不全。此外,来自肾上腺质量和形态的间接证据表明,醋酸环丙孕酮也可能抑制垂体前叶促肾上腺皮质激素的产生或分泌。