van der Spuy Z M, Jones D L, Wright C S, Piura B, Paintin D B, James V H, Jacobs H S
Clin Endocrinol (Oxf). 1983 Oct;19(4):521-31. doi: 10.1111/j.1365-2265.1983.tb00027.x.
The effects of equivalent doses of two inhibitors of the 3-beta-hydroxy steroid dehydrogenase enzyme system--WIN 24540 (trilostane) and WIN 32729--on the secretion of progesterone in early human pregnancy are described. Patients and controls less than 12 weeks pregnant were given a single dose of either drug and the resultant hormonal changes monitored for 7 1/2 h. A consistent fall in plasma progesterone concentrations occurred at all doses and, at the highest dose, they fell to less than 50% of pre-treatment levels. However, whilst with trilostane the associated increase in plasma concentrations of pregnenolone was always accompanied by a rise in plasma DHA concentrations, with WIN 32729 there appeared to be no adrenal effect at the lower dosage levels. These data demonstrate inhibition of progesterone secretion in human pregnancy using non-hormonally active steroids. The pattern of steroid precursors indicates that while both drugs inhibit 3-beta-hydroxy steroid dehydrogenase activity, WIN 32729 is more selective and only interferes with adrenal steroid biosynthesis at high doses.
本文描述了两种等效剂量的3-β-羟基类固醇脱氢酶系统抑制剂——WIN 24540(曲洛司坦)和WIN 32729——对人类妊娠早期孕酮分泌的影响。对妊娠12周以内的患者及对照者给予单剂量的上述任一药物,并监测随后7.5小时内的激素变化。所有剂量均使血浆孕酮浓度持续下降,在最高剂量时,其降至治疗前水平的50%以下。然而,使用曲洛司坦时,孕烯醇酮血浆浓度的相应升高总是伴随着血浆脱氢表雄酮浓度的升高,而使用WIN 32729时,在较低剂量水平似乎没有肾上腺效应。这些数据表明,使用非激素活性类固醇可抑制人类妊娠期间的孕酮分泌。类固醇前体的模式表明,虽然两种药物均抑制3-β-羟基类固醇脱氢酶活性,但WIN 32729更具选择性,仅在高剂量时干扰肾上腺类固醇生物合成。