Makimura N, Kato K, Seki K, Mitsui C
Endocrinol Jpn. 1984 Jun;31(3):349-53. doi: 10.1507/endocrj1954.31.349.
Changes in the concentrations of progesterone, 17 beta-estradiol and 13, 14-dihydro-15-oxo-prostaglandin F2 alpha (PGFM) were evaluated in the peripheral plasma of rabbits during late pregnancy by treating trilostane, an inhibitor of 3 beta-hydroxysteroid dehydrogenase, in an attempt to obtain further insight into the involvement of progesterone and prostaglandin (PG) in the initiation of parturition. The concentrations of progesterone were 18.8 +/- 2.2 ng/ml (mean +/- SE, n = 6) before administration of the inhibitor, significantly (p less than 0.05) fell to 7.6 +/- 1.0 ng/ml (n = 6) at 30 min, and remained low until 10 h after the drug administration. The concentrations of progesterone were still low (5.4 +/- 0.5 ng/ml, n = 6) at 20-24 h after administration of the inhibitor, and were also low (4.9 +/- 2.2 ng/ml, n = 6) at delivery. Premature deliveries occurred at 28.8 +/- 2.0 h after injection of trilostane (on days 29 of gestation). Increased concentrations of PGFM were observed at delivery. However, administration of trilostane induced no discernible changes in the concentration of estradiol. These findings suggest that delivery is induced by progesterone withdrawal and that synthesis prostaglandin F2 alpha is remarkably increased at delivery in the rabbit.
为了进一步深入了解孕酮和前列腺素(PG)在分娩启动过程中的作用,通过给孕晚期兔子外周血浆注射3β - 羟基类固醇脱氢酶抑制剂曲洛司坦,评估孕酮、17β - 雌二醇和13,14 - 二氢 - 15 - 氧代 - 前列腺素F2α(PGFM)浓度的变化。注射抑制剂前孕酮浓度为18.8±2.2 ng/ml(平均值±标准误,n = 6),30分钟时显著(p<0.05)降至7.6±1.0 ng/ml(n = 6),并在给药后10小时内一直保持较低水平。给药后20 - 24小时孕酮浓度仍较低(5.4±0.5 ng/ml,n = 6),分娩时也较低(4.9±2.2 ng/ml,n = 6)。注射曲洛司坦后28.8±2.0小时(妊娠第29天)出现早产。分娩时观察到PGFM浓度升高。然而,注射曲洛司坦并未引起雌二醇浓度的明显变化。这些发现表明,在兔子中,分娩是由孕酮撤退诱导的,并且分娩时前列腺素F2α的合成显著增加。