Molecular mechanisms of the antihormonal and antiimplantation effects of norethisterone and its a-ring reduced metabolites

✍ Scribed by Ivone Castro; Marco Antonio Cerbón; Ana Maria Pasapera; Ruben GutiéRrez-sagal; Gustavo A. Garcia; Carlos Orozco; Ignacio Camacho-Arroyo; Rene Anzaldua; Gregorio PéRez-Palacios

• Publisher: John Wiley and Sons
• Year: 1995
• Tongue: English
• Weight: 692 KB
• Volume: 40
• Category: Article
• ISSN: 1040-452X
• DOI: 10.1002/mrd.1080400204

✦ Synopsis

Abstract

Norethisterone (NET) has been used as a contragestational postcoital agent. It is biotrans‐formed to 5α dihydro‐NET (5α‐NET) and 3β,5α tetrahydro‐NET (3β,5α‐NET) in target tissues. The participation of these metabolites in NET effects is unknown. We have examined the antiimplantation and antiprogestational effects of NET and its metabolites, in adult mated female rabbits, by assessing the number of implantation sites and the expression products of the uteroglobin (UTG) gene in the uterus, and by comparing them with those of RU‐486 and estradiol. Steroids were daily administered s.c. at several doses for 7 consecutive days, starting 24 hr after coitus. To assure that fertilization occurred in all animals, the presence of early pregnancy factor was determined. The results demonstrated that high doses (5 mg/kg) of NET reduced both implantation and the expression of the UTG gene. On the other hand, lower doses (1.5 mg/kg) of 5α‐NET produced an antiimplantation effect and suppressed UTG synthesis and its mRNA. These effects were similar to those of RU‐486. At lower doses (1 mg/kg), both estradiol and the estrogenic metabolite 3β,5α‐NET were also effective in inhibiting implantation and UTG gene expression. The overall results suggest that NET metabolites exert antiimplantation and antiprogestational effects through their interaction with progesterone and estrogen receptors, and provide an explanation for the molecular mechanisms involved in the postcoital contraceptive action of NET. © 1995 Wiley‐Liss, Inc.