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大鼠子宫中内源性和外源性花生四烯酸的前列腺素合成。雌二醇和孕酮的作用。

Prostaglandin synthesis from endogenous and exogenous arachidonic acid in the rat uterus. Effect of estradiol and progesterone.

作者信息

Jouanen A, Saintot M, Thaler-Dao H, Crastes de Paulet A

出版信息

Prostaglandins Leukot Med. 1985 Jun;18(3):321-36. doi: 10.1016/0262-1746(85)90065-4.

Abstract

Regulation of uterine prostaglandin (PG) synthesis by steroid sex hormones was studied in female rats. Animals were ovariectomized (OVX) and received silastic implants of estradiol (E2) or progesterone (Pg); the implants were maintained for 7 days. The animals were sacrificed and their uteri homogenized at 4 degrees C. Basal levels of PGs and PGs synthesized during 20 min incubations at 37 degrees C, either without exogenous arachidonic acid (AA), or in the presence of 2.10(-5)M added AA were measured by RIA. Comparison between the various treatments shows that the regulation of uterine PG synthesis in the rat is a multistep process and depends on the type of PG. PGI2 (6 keto PGF1 alpha) is synthesised in very large amounts but is not very significantly influenced by hormonal treatment. PGF2 alpha and PGE2 are synthesized in much smaller quantities but are very dependent on hormonal treatment. E2 stimulates PGF2 alpha and inhibits PGE2, shifting the ratio from 0.5 in untreated OVX rats to 3.3 in OVX E2-treated rats. TXA2 (TXB2) is stimulated by E2. Pg significantly stimulates endogenous PGF2 alpha levels but does not change the profile of PGs synthesized from the endogenous substrate. It inhibits PGE2 synthesis from exogenously added AA. These results show that E2 favors PGF2 alpha synthesis at the expense of PGE2 and that the synthesis of PGI2, which is the main AA metabolite in the rat uterus is not hormone dependent, (at least not under the conditions of our experiments).

摘要

在雌性大鼠中研究了甾体性激素对子宫前列腺素(PG)合成的调节作用。将动物进行卵巢切除(OVX),并植入雌二醇(E2)或孕酮(Pg)的硅橡胶植入物;植入物维持7天。处死动物,将其子宫在4℃下匀浆。通过放射免疫分析法(RIA)测量PG的基础水平以及在37℃下孵育20分钟期间合成的PG,孵育时要么不添加外源性花生四烯酸(AA),要么添加2.10(-5)M的AA。各种处理之间的比较表明,大鼠子宫PG合成的调节是一个多步骤过程,并且取决于PG的类型。前列环素I2(6-酮-前列腺素F1α)大量合成,但受激素处理的影响不是很显著。前列腺素F2α和前列腺素E2合成量少得多,但非常依赖于激素处理。E2刺激前列腺素F2α并抑制前列腺素E2,使该比例从未经处理的OVX大鼠中的0.5转变为经OVX E2处理的大鼠中的3.3。血栓素A2(TXB2)受E2刺激。Pg显著刺激内源性前列腺素F2α水平,但不改变从内源性底物合成的PG的谱。它抑制从外源性添加的AA合成前列腺素E2。这些结果表明,E2有利于以牺牲前列腺素E2为代价的前列腺素F2α合成,并且前列环素I2(大鼠子宫中主要的AA代谢产物)的合成不依赖激素,(至少在我们的实验条件下不依赖)。

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