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分娩期大鼠子宫中前列腺素合成增加及其对子宫肌层催产素受体浓度的影响。

Enhanced prostaglandin synthesis in the parturient rat uterus and its effects on myometrial oxytocin receptor concentrations.

作者信息

Chan W Y

机构信息

Department of Pharmacology, Cornell University Medical College, New York, New York 10021.

出版信息

Prostaglandins. 1987 Dec;34(6):889-902. doi: 10.1016/0090-6980(87)90069-4.

Abstract

We measure oxytocin (OT) responsiveness and prostaglandins (PGs) synthesis in uteri of 19, 20, 21 and 22-day pregnant and 2-day postpartum rats to determine whether the enhanced OT sensitivity and PG synthesis in the parturient uterus is the result of a higher cyclooxygenase activity. We also investigated the effects of suppression of PG synthesis on OT responsiveness and OT receptor in 22-day and 23-day pregnant rats. PG productions (PGE2, PGF2 alpha, 6-keto-PGF1 alpha and TXB2 in microsomal fractions were quantitated by radio- immunoassays (RIAs). OT receptor concentrations were measured in plasma membrane fractions by radioligand-receptor binding assays. Naproxen sodium was used to inhibit endogenous PG synthesis. We found a close temporal relationship between enhanced OT responsiveness and increased uterine PGE2 alpha synthesis, but no significant difference in cyclooxygenase activities among the microsomes prepared from uteri of different gestational ages. Suppression of PG synthesis attenuated OT responsiveness and markedly reduced OT binding sites, from 242 to 78 fmol/mg protein. There was no change in the binding affinity. These findings suggest that PG stimulates OT receptor formation which leads to enhanced OT responsiveness. The increase in PG production is not mediated by a higher cyclooxygenase activity.

摘要

我们检测了妊娠19、20、21和22天以及产后2天大鼠子宫中催产素(OT)反应性和前列腺素(PGs)合成,以确定分娩期子宫中OT敏感性增强和PG合成增加是否是由于环氧化酶活性升高所致。我们还研究了抑制PG合成对妊娠22天和23天大鼠OT反应性和OT受体的影响。通过放射免疫分析(RIAs)对微粒体部分中的PG产物(PGE2、PGF2α、6-酮-PGF1α和TXB2)进行定量。通过放射性配体-受体结合分析测量质膜部分中的OT受体浓度。萘普生钠用于抑制内源性PG合成。我们发现OT反应性增强与子宫PGE2α合成增加之间存在密切的时间关系,但不同妊娠龄子宫制备的微粒体中环氧化酶活性无显著差异。抑制PG合成可减弱OT反应性,并显著减少OT结合位点,从242 fmol/mg蛋白质降至78 fmol/mg蛋白质。结合亲和力没有变化。这些发现表明,PG刺激OT受体形成,从而导致OT反应性增强。PG产生的增加不是由较高的环氧化酶活性介导的。

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