Jellinck P H, Newcombe A M, Lyttle C R
Department of Biochemistry, Queen's University, Kingston, Ontario.
J Steroid Biochem Mol Biol. 1993 Apr;45(4):303-7. doi: 10.1016/0960-0760(93)90346-x.
The contragestational steroid RU 486 enhanced the increase in peroxidase activity produced by estradiol in estrogen-primed immature rat uteri and, like the antiandrogen flutamide, RU 486 reversed the inhibitory effect of testosterone on this estrogen-induced response. It antagonized the inhibition produced by progesterone but had no effect on peroxidase induction by itself or in unprimed immature animals. RU 486 also enhanced the effect of estradiol on the synthesis of complement component C3 in the rat uterus. The results confirm that RU 486 possesses antiandrogenic as well as antiprogestational properties. They also suggest that, in normal adult animals, the increase in peroxidase activity in the uterus in response to estrogen is not expressed fully but held in check by other endogenous steroids acting through their individual receptors.
抗孕甾体RU 486增强了雌激素预处理的未成熟大鼠子宫中由雌二醇引起的过氧化物酶活性的增加,并且与抗雄激素氟他胺一样,RU 486逆转了睾酮对这种雌激素诱导反应的抑制作用。它拮抗孕酮产生的抑制作用,但对自身或未预处理的未成熟动物中的过氧化物酶诱导没有影响。RU 486还增强了雌二醇对大鼠子宫中补体成分C3合成的作用。结果证实RU 486具有抗雄激素以及抗孕激素特性。它们还表明,在正常成年动物中,子宫中对雌激素反应的过氧化物酶活性增加并未完全表达,而是受到通过其各自受体起作用的其他内源性甾体的抑制。