Bygdeman M, Swahn M L, Gemzell-Danielsson K, Svalander P
Department of Obstetrics and Gynecology, Karolinska Hospital, Stockholm, Sweden.
Ann Med. 1993 Feb;25(1):61-4. doi: 10.3109/07853899309147859.
RU 486 is a 19-norsteroid which has a specific high affinity binding to the progesterone and glucocorticoid receptor. It is generally accepted that RU 486 acts as a pure progesterone antagonist almost without agonistic activity. RU 486 acts mainly directly on the target organ, such as the endometrium, but also to some extent indirectly through an effect on the pituitary gonadotrophin secretion. The effect of RU 486 during the menstrual cycle is dependent on time of treatment. Treatment before ovulation will result in a prolongation of the proliferative phase of the menstrual cycle, while treatment during the mid- and late luteal phase will invariably induce bleeding, often followed by a second bleeding episode at the expected time of menstruation. The only treatment period which does not influence the menstrual cycle is treatment immediately following ovulation. Treatment during the proliferative phase has no effect on endometrial morphology but inhibits follicular development and delays oestrogen and LH surge. Treatment on the first days following ovulation has no effect on ovarian steroid concentration, but will significantly delay endometrial development, cause a change in the concentration of oestrogen and progesterone receptor concentration enzyme activity and production of substances thought to be progesterone dependent. The change in endometrial development is sufficient to prevent implantation. In mid- and late luteal phase, treatment with RU 486 will result in endometrial shedding in spite of normal progesterone levels. Post-ovulatory treatment with RU 486 will also significantly change uterine contractility. In early pregnancy, withdrawal of progesterone inhibition will result in uterine contractility and a significant increase in the sensitivity of the myometrium to prostaglandin.(ABSTRACT TRUNCATED AT 250 WORDS)
米非司酮是一种19-去甲甾体,它对孕酮和糖皮质激素受体具有特异性高亲和力结合。一般认为,米非司酮几乎没有激动活性,可作为一种纯孕酮拮抗剂。米非司酮主要直接作用于靶器官,如子宫内膜,但也在一定程度上通过影响垂体促性腺激素分泌间接发挥作用。米非司酮在月经周期中的作用取决于治疗时间。排卵前治疗会导致月经周期增殖期延长,而黄体中期和后期治疗则总是会引发出血,通常在预期月经时间还会出现第二次出血。唯一不影响月经周期的治疗时期是排卵后立即治疗。增殖期治疗对子宫内膜形态没有影响,但会抑制卵泡发育并延迟雌激素和促黄体生成素高峰。排卵后第一天治疗对卵巢甾体浓度没有影响,但会显著延迟子宫内膜发育,导致雌激素和孕酮受体浓度、酶活性以及被认为依赖孕酮的物质产生发生变化。子宫内膜发育的变化足以防止着床。在黄体中期和后期,尽管孕酮水平正常,但用米非司酮治疗会导致子宫内膜脱落。排卵后用米非司酮治疗也会显著改变子宫收缩力。在妊娠早期,撤除孕酮抑制会导致子宫收缩力增强,子宫肌层对前列腺素的敏感性显著增加。(摘要截选至250词)