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恒河猴黄体期早期给予米非司酮的矛盾作用。

Contranidatory activity of early luteal phase administration of mifepristone in the rhesus monkey.

作者信息

Ghosh D, De P, Sengupta J

机构信息

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

出版信息

Indian J Physiol Pharmacol. 1993 Jan;37(1):13-8.

PMID:8449539
Abstract

The contranidatory action of mifepristone (RU 486) given as a single application at different dosages to mated rhesus monkeys (Macaca mulatta) on second day after ovulation has been examined in the present study. In group 1, monkeys (n = 3) received only vehicle (benzyl benzoate: olive oil, 1:4, v/v) and were treated as controls. In group 2 monkeys (n = 4), RU 486 was given by gavage at 10 mg/kg in group 4 (n = 5). The patterns of cycles and profiles of serum estrogen and progesterone were monitored for assessing the occurrence of implantation and pregnancy. At a single dose of 10 mg/kg, RU 486 was found to be ineffective in preventing nidation, resulting pregnancy in three females out of four treated monkeys. Similarly, an s.c. administration of 1 mg/kg could provide pregnancy protection in two of the four treated monkeys. In these monkeys, however, the menstrual cycle characteristics were not affected as compared to pretreatment cycles. Interestingly, the administration of 2 mg/kg, s.c., RU 486 could provide a hundred percent pregnancy protection in mated monkeys, and there was no significant changes in the pattern of menstrual cycle characteristics. It appears that an early post-ovulatory administration of RU 486 may be successfully used in human as an effective once-a-month, early luteal phase contranidatory agent.

摘要

本研究考察了在排卵后第二天给交配后的恒河猴(猕猴)单次应用不同剂量米非司酮(RU 486)的对抗作用。在第1组中,猴子(n = 3)仅接受赋形剂(苯甲酸苄酯:橄榄油,1:4,v/v)并作为对照。在第2组猴子(n = 4)中,第4组(n = 5)以10 mg/kg的剂量通过灌胃给予RU 486。监测周期模式以及血清雌激素和孕酮水平,以评估着床和妊娠情况。发现单次剂量为10 mg/kg时,RU 486在预防着床方面无效,4只接受治疗的猴子中有3只怀孕。同样,皮下注射1 mg/kg可使4只接受治疗的猴子中的2只得到妊娠保护。然而,与治疗前的周期相比,这些猴子的月经周期特征未受影响。有趣的是,皮下注射2 mg/kg的RU 486可使交配后的猴子得到100%的妊娠保护,且月经周期特征模式无显著变化。看来排卵后早期应用RU 486可能作为一种有效的每月一次的黄体期早期对抗剂成功应用于人类。

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