Ishwad P C, Katkam R R, Hinduja I N, Chwalisz K, Elger W, Puri C P
Institute for Research in Reproduction (ICMR), Parel, Bombay, India.
Contraception. 1993 Jul;48(1):57-70. doi: 10.1016/0010-7824(93)90066-g.
The effects of an antiprogestin ZK 98.299 (onapristone) on serum levels of estradiol and progesterone, and on the endometrial morphology were studied in adult bonnet monkeys. Twelve animals having menstrual cycles of normal duration (24 to 30 days) were randomly distributed into 4 equal groups. The animals in Group 1 were treated (s.c.) with the vehicle (benzyl benzoate: castor oil, 1:10), and in Groups 2, 3 and 4 with 5 mg, 10 mg, or 20 mg ZK 98.299 once-a-week, respectively. Treatment was initiated on day 1 of the menstrual cycle and each animal in Groups 1, 2 and 3 was treated for two consecutive cycles. Since the treatment cycle length of animals in Group 4 was considerably prolonged, they were treated for one menstrual cycle only. Endometrial biopsy was taken around day 20 of the second treatment cycle of first three groups and around day 50 of the 4th group of animals. Treatment with vehicle or 5 mg ZK 98.299 had no significant effect on the menstrual cycle length. Treatment with 10 mg dose had no effect in two animals and prolonged the cycle length in one, whereas, further increase in the dose to 20 mg prolonged the cycle length in all the animals. The duration of menses was generally reduced. Treatment with vehicle or different doses of ZK 98.299 had no effect on ovulation. In animals treated with 5 or 10 mg dose, the pattern of mid cycle rise in serum estradiol levels and progesterone levels during the luteal phase of both treatment cycles were comparable to those of vehicle-treated animals and were suggestive of normal ovulatory cycles. On the other hand, in animals treated with the higher dose (20 mg/week), progesterone levels during the luteal phase were significantly reduced and were indicative of luteal insufficiency. The hormonal data during the treatment period of this group of animals was suggestive of two distinct ovarian cycles indicating that the menstrual bleeding during the treatment period was probably very scanty. Treatment with ZK 98.299 impaired the endometrial development in a dose-dependent manner. In vehicle-treated animals, the endometrium had large and tortous glands with secretions. Treatment with ZK 98.299 caused atrophic changes in the glands as well as in the stroma. The height of the epithelial cells was markedly decreased and they became small and inactive. This study, therefore, suggests that treatment with low doses of antiprogestin ZK 98.299 at weekly intervals does not block folliculogenesis or ovulation, but has an inhibitory effect on the endometrium.(ABSTRACT TRUNCATED AT 250 WORDS)
在成年冠毛猕猴中研究了抗孕激素ZK 98.299(奥那司酮)对雌二醇和孕酮血清水平以及子宫内膜形态的影响。将12只月经周期正常(24至30天)的动物随机分为4组,每组数量相等。第1组动物皮下注射赋形剂(苯甲酸苄酯:蓖麻油,1:10),第2、3和4组动物分别每周一次皮下注射5毫克、10毫克或20毫克ZK 98.299。在月经周期第1天开始治疗,第1、2和3组的每只动物连续治疗两个周期。由于第4组动物的治疗周期明显延长,所以它们仅接受一个月经周期的治疗。在前三组动物第二个治疗周期的第20天左右以及第4组动物的第50天左右进行子宫内膜活检。用赋形剂或注射5毫克ZK 98.299治疗对月经周期长度无显著影响。用10毫克剂量治疗时,两只动物无影响,一只动物的周期长度延长;而将剂量进一步增加到20毫克时,所有动物的周期长度均延长。月经持续时间总体缩短。用赋形剂或不同剂量的ZK 98.299治疗对排卵无影响。用5毫克或10毫克剂量治疗的动物,在两个治疗周期的黄体期,血清雌二醇水平和孕酮水平的中期升高模式与用赋形剂治疗的动物相当,提示排卵周期正常。另一方面,用高剂量(20毫克/周)治疗的动物,黄体期的孕酮水平显著降低,表明黄体功能不全。该组动物治疗期间的激素数据提示有两个不同的卵巢周期,表明治疗期间的月经出血可能很少。ZK 98.299治疗以剂量依赖的方式损害子宫内膜发育。在用赋形剂治疗的动物中,子宫内膜有大而弯曲的腺体且有分泌物。ZK 98.299治疗导致腺体以及基质出现萎缩性变化。上皮细胞高度明显降低,变得小且不活跃。因此,本研究表明,每周间隔使用低剂量抗孕激素ZK 98.299不会阻断卵泡生成或排卵,但对子宫内膜有抑制作用。(摘要截选至250词)