Croxatto H B, Salvatierra A M, Romero C, Spitz I M
Instituto Chileno de Medicina Reproductiva, Universidad de Chile, Santiago.
J Clin Endocrinol Metab. 1987 Dec;65(6):1272-7. doi: 10.1210/jcem-65-6-1272.
RU486, a 19-nor steroid, binds with high affinity to the receptors for progesterone and glucocorticoids, blocking the actions of these hormones on their target tissues. We conducted studies to determine whether RU486 administered at the end of the luteal phase would disturb the menstrual rhythm, ovulation, or hormonal parameters in the treatment and post-treatment cycles. The first study was done in six surgically sterilized women during two consecutive cycles. RU486 [17 beta-hydroxy-11 beta-(4-dimethylaminophenyl)17 alpha-(1-propynyl)estra-4,9-dien-3-one; 100 mg/day] was given for 4 consecutive days, commencing on days 23-27 of the first cycle. Menstrual bleeding occurred by the second day of RU486 administration in all women and was indistinguishable from their usual bleeding pattern. The onset of this bleeding was advanced by RU486 administration, since it entailed shortening of the luteal phase with prolongation of the following follicular phase. Serum LH, FSH, estradiol, and progesterone levels were normal in five of the six women in both the treatment and posttreatment cycles. The second study was conducted in 10 women who were not exposed to the risk of pregnancy. RU486 (100 mg/day) was given for 4 consecutive days, commencing 4 days before their expected menses for 3 successive cycles, preceded and followed by 2 placebo-treated cycles. Bleeding patterns were indistinguishable during the RU486 and placebo cycles. Late luteal phase administration of RU486 consistently produced menstrual bleeding within 1-3 days of drug administration. Daily early morning urinary LH excretion in 6 women and estrone glucuronide and pregnanediol glucuronide excretion in 5 women during both placebo and RU486 cycles were consistent with luteinization, suggesting ovulation and appropriate corpus luteum function. We conclude that RU486 has no major effect on menstrual cycle events if given at the time of the natural progesterone withdrawal that occurs before menses in nonpregnant women.
RU486是一种19-去甲甾体,它与孕酮和糖皮质激素的受体具有高亲和力,可阻断这些激素对其靶组织的作用。我们进行了多项研究,以确定在黄体期末期给予RU486是否会扰乱治疗周期及治疗后周期的月经节律、排卵或激素参数。第一项研究在6名接受过手术绝育的女性中进行,为期两个连续周期。RU486[17β-羟基-11β-(4-二甲基氨基苯基)-17α-(1-丙炔基)雌甾-4,9-二烯-3-酮;100毫克/天]连续给药4天,从第一个周期的第23至27天开始。所有女性在服用RU486的第二天就出现了月经出血,且与她们通常的出血模式没有区别。这种出血的发生因服用RU486而提前,因为这导致黄体期缩短,随后的卵泡期延长。在治疗周期和治疗后周期中,6名女性中有5名的血清促黄体生成素(LH)、促卵泡生成素(FSH)、雌二醇和孕酮水平均正常。第二项研究在10名没有妊娠风险的女性中进行。RU486(100毫克/天)连续给药4天,在她们预期月经前4天开始,连续进行3个周期,前后各有2个安慰剂治疗周期。在RU486周期和安慰剂周期中,出血模式没有区别。在黄体期末期给予RU486始终会在给药后1至3天内引起月经出血。在安慰剂周期和RU486周期中,6名女性的每日清晨尿LH排泄量以及5名女性的雌酮葡萄糖醛酸苷和孕二醇葡萄糖醛酸苷排泄量均与黄体化一致,表明有排卵和适当的黄体功能。我们得出结论,在未怀孕女性月经前自然孕酮撤退时给予RU486,对月经周期事件没有重大影响。