Franchi A M, Gimeno A L, Gimeno M A
Centro de Estudios Farmacológicos y de Principios Naturales (CEFAPRIN), Universidad de Buenos Aires, Argentina.
Prostaglandins Leukot Essent Fatty Acids. 1989 Apr;36(1):25-9. doi: 10.1016/0952-3278(89)90158-0.
The effects of 17-beta estradiol and of some catechol and non-catechol-estrogens on the synthesis and output of prostaglandins (PGs) E and F by uteri from ovariectomized rats, were explored. Uteri from castrated animals released twice as much PGE than PGF. When uterine tissue was obtained from spayed rats injected prior to sacrifice with a low dose of 17-beta estradiol (0.5 + 1.0 microgram, on two consecutive days), the output of PGE diminished significantly. With a higher dose of the hormone (0.5 + 50.0 micrograms) the depressive influence on the synthesis and release of PGE was even more marked, whereas the output of PGF rose significantly. Low or high doses of estrone or of estriol failed to affect the release of either one of the PGs determined. On the other hand, 2-0H-estradiol at a low dose had no action but at a higher one inhibited the release of PGE without influencing PGF. Neither low nor high doses of 2-0H estriol or of 2-0H estrone affected the synthesis and release of uterine PGs. It was also observed that all the compounds tested evoked a significant uterotrophic action. It appears plausible that some catechol metabolites of 17-beta estradiol, but not other catechol-estrogens, could be involved in the mechanism of action of 17-beta estradiol modulating the production of PGs by the rat uterus.
研究了17-β-雌二醇以及某些儿茶酚和非儿茶酚雌激素对去卵巢大鼠子宫前列腺素(PGs)E和F合成及释放的影响。去势动物的子宫释放的PGE是PGF的两倍。当从在处死前连续两天注射低剂量17-β-雌二醇(0.5 + 1.0微克)的去势大鼠获取子宫组织时,PGE的释放显著减少。使用更高剂量的激素(0.5 + 50.0微克)时,对PGE合成和释放的抑制作用更为明显,而PGF的释放则显著增加。低剂量或高剂量的雌酮或雌三醇均未影响所测定的任何一种PG的释放。另一方面,低剂量的2-OH-雌二醇无作用,但高剂量时抑制PGE的释放而不影响PGF。低剂量或高剂量的2-OH-雌三醇或2-OH-雌酮均不影响子宫PG的合成和释放。还观察到所有测试化合物均引起显著的子宫营养作用。似乎17-β-雌二醇的某些儿茶酚代谢产物而非其他儿茶酚雌激素可能参与了17-β-雌二醇调节大鼠子宫PG产生的作用机制。