Effect of antiestrogen CI-628 on the morphology and 17β-hydroxysteroid dehydrogenase activity of mouse blastocysts in culture

The effect of CI-628 on the morphology and 17β-hydroxysteroid dehydrogenase (17β-HSD) activity of mouse blastocysts were compared in culture. When Day 4 mouse blastocysts were cultured in Eagle's medium containing 214 ng 3H-estradiol (E 2) and CI-628 at 0, 1.5, 3, 6, 12 and 18 μg/ml, shedding o...

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Veröffentlicht in:Contraception (Stoneham) 1984-09, Vol.30 (3), p.271-278
Hauptverfasser: Wu, J.T., Doong, R.L.
Format: Artikel
Sprache:eng
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Zusammenfassung:The effect of CI-628 on the morphology and 17β-hydroxysteroid dehydrogenase (17β-HSD) activity of mouse blastocysts were compared in culture. When Day 4 mouse blastocysts were cultured in Eagle's medium containing 214 ng 3H-estradiol (E 2) and CI-628 at 0, 1.5, 3, 6, 12 and 18 μg/ml, shedding of the zona pellucida was prevented by CI-628. The effect of CI-628 on the morphology was dose-dependent: little effects were seen at 1.5 and 3 μg/ml during the first 2 days, but the blastocysts became small, dense and eventually collapsed inside the zona. At 6 μg/ml and higher, the effect was quite pronounced. The earliest change was seen at 10 hours in 12 and 18 μg/ml CI-628 medium when 1 3 of the embryos became dense and smaller. All were collapsed by 22 h. CI-628 reduced the 17β-HSD activity slightly during the first 5 h. Nevertheless, the enzyme activity continued to increase, though at a slower rate than the control (0 μg/ml) group, up to 22 h in the 12 and 18 μg/ml group, and up to 46 h in the 1.5, 3 and 6 μg/ml group. In the latter 3 groups, the 17β-HSD activity remained fairly high throughout the culture. It appears that, in comparison with the morphology, the 17β-HSD activity is relatively resistant to CI-628 effects. In the blastocyst homogenate, CI-628 had no effect on E 2→E 1 conversion. It is concluded that CI-628 causes degeneration of blastocysts through mechanisms other than interfering with 17β-HSD activities.
ISSN:0010-7824
1879-0518
DOI:10.1016/0010-7824(84)90090-8