Literature DB >> 1331167

Inhibition of ovulation by low-dose mifepristone (RU 486).

W L Ledger1, V M Sweeting, H Hillier, D T Baird.   

Abstract

Mifepristone (RU 486) is a potent antigestagen and antiglucocorticoid which when given at a dose of 25-600 mg disrupts folliculogenesis, inhibits ovulation and induces menses in healthy women. This study reports the effects of much lower doses of mifepristone than used previously, given for the duration of a complete menstrual cycle. Healthy female volunteers (n = 11) with regular menstrual cycles were given mifepristone at a daily dose of 5 mg (n = 6) or 2 mg (n = 5) for 30 days, beginning immediately after an ovulatory placebo cycle. Mifepristone prevented menstruation for the duration of the treatment period, with recurrence of menses 15-29 days after replacement of mifepristone with placebo. Daily mifepristone given in either 5 mg or 2 mg doses inhibited ovulation, as indicated by the lack of a rise in urinary pregnanediol excretion. The excretion of oestrone glucuronide in urine rose during treatment, suggesting ovarian follicular development. Inhibition of ovulation appeared to result from a failure of the positive feedback effect of oestradiol on the hypothalamo-pituitary axis, as no surges of luteinizing hormone were seen despite pre-ovulatory levels of oestrone glucuronide being measured during exposure to mifepristone. The cycle immediately following treatment was shorter than the pre-treatment cycle, with lower peak levels of pregnanediol glucuronide, suggesting an inadequate luteal phase. Recovery from the effects of mifepristone treatment was more rapid after 2 mg than after 5 mg and one subject conceived in the immediate post-treatment phase, indicating adequate ovulation and luteinization.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Keywords:  Biology; Clinical Research; Comparative Studies; Contraception; Contraceptive Mode Of Action; Developed Countries; Endocrine System; Estradiol; Estrogens; Estrone; Europe; Family Planning; Gonadotropins; Gonadotropins, Pituitary; Hormone Antagonists; Hormones; Luteinizing Hormone; Menstrual Cycle; Menstruation; Northern Europe; Ovulation Suppression; Physiology; Prospective Studies; Reproduction; Research Methodology; Research Report; Ru-486; Scotland; Studies; United Kingdom

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Substances:

Year:  1992        PMID: 1331167     DOI: 10.1093/oxfordjournals.humrep.a137776

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  6 in total

1.  Clinical pharmacokinetics of mifepristone.

Authors:  O Heikinheimo
Journal:  Clin Pharmacokinet       Date:  1997-07       Impact factor: 6.447

2.  Emergency contraception: potential role of ulipristal acetate.

Authors:  Kristina Gemzell-Danielsson; Chun-Xia Meng
Journal:  Int J Womens Health       Date:  2010-08-09

Review 3.  Antiprogestin pharmacodynamics, pharmacokinetics, and metabolism: implications for their long-term use.

Authors:  G R Jang; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1997-12

4.  Mifepristone 5 mg versus 10 mg for emergency contraception: double-blind randomized clinical trial.

Authors:  Josep Lluis Carbonell; Ramon Garcia; Adriana Gonzalez; Andres Breto; Carlos Sanchez
Journal:  Int J Womens Health       Date:  2015-01-12

Review 5.  Clinical Utility of Mifepristone: Apprising the Expanding Horizons.

Authors:  Zalak V Karena; Harsh Shah; Hetvee Vaghela; Kalp Chauhan; Pranav K Desai; Asjad Raza Chitalwala
Journal:  Cureus       Date:  2022-08-23

6.  Aglepristone Administration in Mid-Proestrus Reduces the LH Peak but Does Not Prevent Ovulation in the Bitch.

Authors:  Piotr Socha; Katarzyna Bladowska; Sławomir Zduńczyk; Tomasz Janowski
Journal:  Animals (Basel)       Date:  2021-06-28       Impact factor: 2.752

  6 in total

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