Scirpa P, Mango D, Bompiani A
J Endocrinol Invest. 1979 Jan-Mar;2(1):83-5. doi: 10.1007/BF03349281.
The in vitro effects of dehydroepiandrosterone (DHA) and allylestrenol on human placental delta 5- 3 beta-hydroxysteroid dehydrogenase, delta 4,5 isomerase activity (delta 5-3 beta-HSDH) was investigated by incubation of subcellular fractions with [4-14C] pregnenolone. It has been found that DHA inhibits the delta 5-3 beta-HSDH activity up to -81% at 5 X 10-5 M concentration while allylestrenol seems to be able to lightly stimulate the delt a 5-3 beta-HSDH activity with a maximum effect (+15-26%) at 5 X 10-7 M concentration. The data concerning allylestrenol, seem of particular interest as this compound is used as a progestative drug during pregnancy, if one consider the inhibitory effect exerted by several natural and synthetic steroids on the delta 5-3 beta-HSDH activity.
通过将亚细胞组分与[4-¹⁴C]孕烯醇酮一起孵育,研究了脱氢表雄酮(DHA)和烯丙雌醇对人胎盘δ⁵-3β-羟基类固醇脱氢酶、δ⁴,⁵异构酶活性(δ⁵-3β-HSDH)的体外作用。已发现,在5×10⁻⁵M浓度下,DHA对δ⁵-3β-HSDH活性的抑制率高达-81%,而烯丙雌醇似乎能够在5×10⁻⁷M浓度下轻度刺激δ⁵-3β-HSDH活性,最大效应为(+15-26%)。考虑到几种天然和合成类固醇对δ⁵-3β-HSDH活性的抑制作用,关于烯丙雌醇的数据似乎特别有趣,因为该化合物在孕期用作孕激素药物。