THE PROGESTERONE ANTAGONIST RU-486 - A POTENTIAL NEW CONTRACEPTIVE AGENT

被引:78
作者
NIEMAN, LK
CHOATE, TM
CHROUSOS, GP
HEALY, DL
MORIN, M
RENQUIST, D
MERRIAM, GR
SPITZ, IM
BARDIN, CW
BAULIEU, EE
LORIAUX, DL
机构
[1] NICHHD, PREGNANCY RES BRANCH, BETHESDA, MD 20892 USA
[2] NIH, DIV RES SERV, VET RESOURCES BRANCH, BETHESDA, MD 20205 USA
[3] POPULAT COUNCIL, CTR BIOMED RES, NEW YORK, NY USA
[4] UNIV PARIS II, HORMONES LAB, PARIS, FRANCE
关键词
D O I
10.1056/NEJM198701223160404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since progesterone supports endometrial nidation of the fertilized ovum, a progesterone antagonist would theoretically block this process and thus have contraceptive potential. We have explored the ability of Ru 486, a newly developed competitive progesterone antagonist to function as a contraceptive agent. A single oral dose of 10 mg per kilogram of body weight given in the midluteal phase consistently induced menses within 72 hours in women with normal cycles and no risk of pregnancy. Bleeding was not prevented by administration of human chorionic gonadotropin in the midluteal phase. This suggested that giving a single dose of RU 486 late in the menstrual cycle might be an effective contraceptive strategy. This concept was tested in monkeys. When given to rhesus females on day 25 of the cycle, a single intramuscular dose of RU 486 (5 mg per kilogram) prevented pregnancy. The vehicle-treated control animals had a 28 percent pregnancy rate (P < 0.05 by chi-square analysis). No side effects were noted in women or monkeys. These data suggest that a progesterone antagonist such as RU 486 has the potential to be an effective, safe, and convenient contraceptive agent. Further work will be necessary to assess the safety of long-term monthly administration and to define the optimal dose and time of administration in women.
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收藏
页码:187 / 191
页数:5
相关论文
共 24 条
[1]   RADIOIMMUNOASSAY OF PLASMA PROGESTERONE [J].
ABRAHAM, GE ;
SWERDLOFF, R ;
TULCHINSKY, D ;
ODELL, WD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1971, 32 (05) :619-+
[2]   THE NEW STEROID ANALOG RU486 INHIBITS GLUCOCORTICOID ACTION IN MAN [J].
BERTAGNA, X ;
BERTAGNA, C ;
LUTON, JP ;
HUSSON, JM ;
GIRARD, F .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1984, 59 (01) :25-28
[3]  
BRODY SA, 1984, 1984 P SOC GYN INV S, P231
[4]   TERMINATION OF EARLY-PREGNANCY BY THE PROGESTERONE ANTAGONIST RU-486 (MIFEPRISTONE) [J].
COUZINET, B ;
LESTRAT, N ;
ULMANN, A ;
BAULIEU, EE ;
SCHAISON, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (25) :1565-1570
[5]   TUBAL INFERTILITY AND THE INTRAUTERINE-DEVICE [J].
CRAMER, DW ;
SCHIFF, I ;
SCHOENBAUM, SC ;
GIBSON, M ;
BELISLE, S ;
ALBRECHT, B ;
STILLMAN, RJ ;
BERGER, MJ ;
WILSON, E ;
STADEL, BV ;
SEIBEL, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (15) :941-947
[6]   PRIMARY TUBAL INFERTILITY IN RELATION TO THE USE OF AN INTRAUTERINE-DEVICE [J].
DALING, JR ;
WEISS, NS ;
METCH, BJ ;
CHOW, WH ;
SODERSTROM, RM ;
MOORE, DE ;
SPADONI, LR ;
STADEL, BV .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (15) :937-941
[7]   NEUROENDOCRINE REGULATION OF THE CORPUS-LUTEUM IN THE HUMAN - EVIDENCE FOR PULSATILE PROGESTERONE SECRETION [J].
FILICORI, M ;
BUTLER, JP ;
CROWLEY, WF .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (06) :1638-1647
[8]   RU-486 - A STEROID WITH ANTIGLUCOCORTICOSTEROID ACTIVITY THAT ONLY DISINHIBITS THE HUMAN PITUITARY-ADRENAL SYSTEM AT A SPECIFIC TIME OF DAY [J].
GAILLARD, RC ;
RIONDEL, A ;
MULLER, AF ;
HERRMANN, W ;
BAULIEU, EE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (12) :3879-3882
[9]   ENDOMETRIAL AND PITUITARY RESPONSES TO THE STEROIDAL ANTIPROGESTIN RU-486 IN POSTMENOPAUSAL WOMEN [J].
GRAVANIS, A ;
SCHAISON, G ;
GEORGE, M ;
DEBRUX, J ;
SATYASWAROOP, PG ;
BAULIEU, EE ;
ROBEL, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1985, 60 (01) :156-163
[10]  
HEALY DL, 1983, FERTIL STERIL, V40, P253