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氢化可的松、雌二醇和孕酮对体外灌流的豚鼠子宫经A23187刺激后前列腺素释放量的影响。

Effects of hydrocortisone, oestradiol and progesterone on A23187-stimulated prostaglandin output from the guinea-pig uterus superfused in vitro.

作者信息

Poyser N L

出版信息

Prostaglandins. 1987 Jan;33(1):101-12. doi: 10.1016/0090-6980(87)90308-x.

DOI:10.1016/0090-6980(87)90308-x
PMID:3108958
Abstract

Hydrocortisone (10 micrograms/ml) had no effect on the basal outputs and A23187-stimulated outputs of PGF2 alpha, PGE2 and 6-keto-PGF1 alpha from the Day 15 guinea-pig uterus superfused in vitro. These findings indicate that the high output of PGF2 alpha from the guinea-pig uterus during the last one-third of the oestrous cycle is not modulated by the adrenal glucocorticoid hormones. Progesterone (10 micrograms/ml) had no effect on the A23187-induced increases in PG output from the Day 15 guinea-pig uterus. However, oestradiol (10 micrograms/ml but not 1 microgram/ml) significantly reduced the increases in outputs of PGF2 alpha, PGE2 and 6-keto-PGF1 alpha induced by A23187 from the Day 15 guinea-pig uterus, without affecting basal PG outputs. The increase in uterine tone induced by A23187 in the Day 15 guinea-pig uterus was reduced by 20-50% by oestradiol (10 micrograms/ml). The addition of oestradiol (10 micrograms/ml) and progesterone together (10 micrograms/ml) produced the same effects on the Day 15 guinea-pig uterus as oestradiol alone. Oestradiol (10 micrograms/ml) also reduced the A23187-induced increases in PG output from the Day 7 guinea-pig uterus, but did not reduce the increase in uterine tone. Oestradiol (10 micrograms/ml) reduced the increases in outputs of PGF2 alpha, PGE2 and 6-keto-PGF1 alpha induced by exogenous arachidonic acid from the Day 7 and Day 15 guinea-pig uterus. Previous studies have shown that oestradiol is not a cyclo-oxygenase inhibitor. The present findings suggest that oestradiol, at a relatively high concentration, may interfere with the access of arachidonic acid to the cyclo-oxygenase enzyme. This action of oestradiol may explain its anti-luteolytic action when administered to guinea-pigs in large doses after Day 9 of the cycle.

摘要

氢化可的松(10微克/毫升)对体外灌流的第15天豚鼠子宫中PGF2α、PGE2和6-酮-PGF1α的基础分泌量以及A23187刺激的分泌量均无影响。这些发现表明,豚鼠子宫在发情周期最后三分之一时间内PGF2α分泌量高并非由肾上腺糖皮质激素调节。孕酮(10微克/毫升)对第15天豚鼠子宫中A23187诱导的PG分泌增加无影响。然而,雌二醇(10微克/毫升而非1微克/毫升)显著降低了第15天豚鼠子宫中A23187诱导的PGF2α、PGE2和6-酮-PGF1α分泌增加,而不影响基础PG分泌量。第15天豚鼠子宫中A23187诱导的子宫张力增加被雌二醇(10微克/毫升)降低了20%-50%。同时添加雌二醇(10微克/毫升)和孕酮(10微克/毫升)对第15天豚鼠子宫产生的作用与单独使用雌二醇相同。雌二醇(10微克/毫升)也降低了第7天豚鼠子宫中A23187诱导的PG分泌增加,但未降低子宫张力增加。雌二醇(10微克/毫升)降低了第7天和第15天豚鼠子宫中外源性花生四烯酸诱导的PGF2α、PGE2和6-酮-PGF1α分泌增加。先前的研究表明雌二醇不是环氧化酶抑制剂。目前的发现表明,相对高浓度的雌二醇可能会干扰花生四烯酸与环氧化酶的接触。雌二醇的这一作用可能解释了在周期第9天后大剂量给豚鼠注射时其抗黄体溶解作用。

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