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排卵后早期单次给予米非司酮(RU 486)对恒河猴的抗着床作用

Anti-nidatory effect of a single, early post-ovulatory administration of mifepristone (RU 486) in the rhesus monkey.

作者信息

Ghosh D, Sengupta J

机构信息

Department of Physiology, All India Institute of Medical Sciences, New Delhi.

出版信息

Hum Reprod. 1993 Apr;8(4):552-8. doi: 10.1093/oxfordjournals.humrep.a138094.

Abstract

The hypothesis that post-coital administration of mifepristone (RU 486) as a single dose in the early luteal phase can be an effective anti-nidatory strategy was tested using the rhesus monkey as the experimental model. Incidence of pregnancy, vaginal bleeding patterns, profiles of menstrual cyclicity and of serum levels of progesterone and oestrogen were examined following administration of RU 486 as a single dose of 10 mg/kg and 2 mg/kg body weight on the second day after ovulation. In control monkeys (group 1; n = 5) receiving the vehicle alone (benzyl benzoate:olive oil, 1:4, v/v) there was a 60% pregnancy rate. Following s.c. administration of RU 486 at both doses, no pregnancy was recorded in a total of 33 treatment cycles in 12 monkeys. Five monkeys received RU 486 at 10 mg/kg s.c. (group 2) in three consecutive cycles. All animals had complete inhibition of implantation; in addition, the treatment cycle length was prolonged (P < 0.001) due to an extension of the luteal phase. The subsequent follicular phase was unaffected. Mild, premature vaginal bleeding during the luteal phase was recorded in five treatment cycles, 3-5 days after drug application. Though the serum profiles of progesterone and oestrogen in these monkeys showed marked individual variations, there was a characteristic progesterone rebound about 18-20 days after drug administration. Monkeys in group 3 were given RU 486 at 2 mg/kg, s.c. either for three consecutive cycles (group 3a; n = 4) or for two consecutive cycles (group 3b; n = 3). Premature luteal phase vaginal bleeding occurred only in four treatment cycles, within 2-6 days post-treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

以恒河猴作为实验模型,对在黄体期早期单次服用米非司酮(RU 486)可作为一种有效的抗着床策略这一假说进行了测试。在排卵后第二天,分别以10 mg/kg和2 mg/kg体重的单次剂量给予RU 486,之后检查妊娠发生率、阴道出血模式、月经周期概况以及孕酮和雌激素的血清水平。在仅接受赋形剂(苯甲酸苄酯:橄榄油,1:4,v/v)的对照猴(第1组;n = 5)中,妊娠率为60%。在以两种剂量皮下注射RU 486后,12只猴子的总共33个治疗周期均未记录到妊娠。五只猴子在三个连续周期中接受了10 mg/kg皮下注射的RU 486(第2组)。所有动物的着床均被完全抑制;此外,由于黄体期延长,治疗周期长度延长(P < 0.001)。随后的卵泡期未受影响。在五个治疗周期中,给药后3 - 5天记录到黄体期轻度过早阴道出血。尽管这些猴子的孕酮和雌激素血清水平显示出明显的个体差异,但给药后约18 - 20天有特征性的孕酮反弹。第3组猴子以2 mg/kg皮下注射RU 486,连续三个周期(第3a组;n = 4)或连续两个周期(第3b组;n = 3)。仅在四个治疗周期中出现了黄体期过早阴道出血,发生在治疗后2 - 6天内。(摘要截断于250字)

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