Kelly R W, Smith S K
Medical Research Council Unit of Reproductive Biology, University of Edinburgh Centre for Reproductive Biology, Scotland.
Prostaglandins Leukot Med. 1987 Oct;29(2-3):181-6. doi: 10.1016/0262-1746(87)90007-2.
The mechanism by which progesterone inhibits PG production is not clear. In systems using isolated human endometrial fragments, progesterone has been shown to inhibit PG production markedly. We have used such a system to test the action of two antiprogesterone steroids RU486 (Roussell-Uclaf) and ZK98734 (Schering) on isolated human endometrial and decidual tissue, with and without added progesterone. Progesterone (200 nM) reduced PGF2 alpha production by the secretory phase endometrium from 10.9 ng/mg tissue/24 hr to 1.9 ng/mg/24hr on the third day of culture (p less than .01) and this effect was antagonised by the addition of either 200 nM RU486 or 200 nM ZK98734 (6.3 and 7.2 ng/mg/24 hr respectively). The antiprogestins on their own showed a slight inhibitory effect on day 3 and RU486 treatment resulted in a significant (p less than .05) decrease in PG production from control. PGE and the main 13,14-dihydro-15-keto metabolites of E and F were also significantly decreased by progesterone and restored by the antiprogestins. The PG production by decidua increased on days 2 and 3 in response to progesterone + antiprogestins but this was not significant. This data shows that the inhibition of PG production shown by progesterone, acting on secretory phase endometrium cultured as tissue fragments, is reversible by the receptor blocking antiprogestins.
孕酮抑制前列腺素(PG)产生的机制尚不清楚。在使用分离的人子宫内膜碎片的系统中,已证明孕酮可显著抑制PG的产生。我们使用这样一个系统来测试两种抗孕酮甾体RU486(罗素 - 优克福公司)和ZK98734(先灵公司)对分离的人子宫内膜和蜕膜组织的作用,分别在添加和不添加孕酮的情况下进行测试。孕酮(200 nM)使分泌期子宫内膜在培养第三天的PGF2α产生量从10.9 ng/mg组织/24小时降至1.9 ng/mg/24小时(p <.01),并且添加200 nM RU486或200 nM ZK98734(分别为6.3和7.2 ng/mg/24小时)可拮抗这种作用。单独使用抗孕酮药物在第三天显示出轻微的抑制作用,并且RU486处理导致PG产生量相对于对照显著降低(p <.05)。孕酮也使PGE以及E和F的主要13,14 - 二氢 - 15 - 酮代谢产物显著减少,而抗孕酮药物可使其恢复。蜕膜的PG产生量在第2天和第3天因孕酮 + 抗孕酮药物而增加,但不显著。这些数据表明,作用于作为组织碎片培养的分泌期子宫内膜的孕酮对PG产生的抑制作用可被受体阻断性抗孕酮药物逆转。