Phillips I D, Fielke S L, Young I R, McMillen I C
Department of Physiology, University of Adelaide, South Australia, Australia.
J Neuroendocrinol. 1996 Dec;8(12):929-33. doi: 10.1111/j.1365-2826.1996.tb00823.x.
The neuroendocrine control of prolactin synthesis and secretion before birth is not well understood. We have measured the changes in the level of prolactin mRNA in the anterior pituitary of the fetal sheep throughout the last 15 days of pregnancy (term = 147 +/- 3 days gestation). We have also investigated the effects of surgical disconnection of the fetal hypothalamus and pituitary (HPD) with or without long term cortisol infusion on pituitary prolactin mRNA levels and plasma prolactin concentrations in the late gestation sheep fetus. Prolactin mRNA levels were measured in anterior pituitaries collected from a series of fetal sheep (130-134 days, n = 6; 135-140 days, n = 6; 141-145 days, n = 6) in late gestation. HPD was carried out in ten fetal sheep at 105-115 days gestation and five intact fetal sheep were used as controls. In the HPD group, either saline (HPD + saline group, n = 5) or cortisol was infused (3.5 mg/24 h) for 5 days from 134-136 days gestation (HPD + cortisol group, n = 5). There was an increase in the ratio of prolactin mRNA: 18S rRNA in the fetal pituitary between 130-134 days (0.46 +/- 0.08, n = 6) and 135-140 days (1.27 +/- 0.17 n = 6) which was maintained after 141 days gestation, (1.27 +/- 0.11, n = 6). The mean prolactin mRNA: 18 S rRNA ratio was significantly higher (P < 0.05) in intact fetal sheep (1.41 +/- 0.16, n = 4) than in the HPD fetal sheep after either saline (0.54 +/- 0.14, n = 4) or cortisol (0.74 +/- 0.24, n = 5) administration. The mean plasma concentration of prolactin was also higher in the intact group (28.3 +/- 3.9 ng/ml) when compared with the HPD + saline group (8.0 +/- 3.3 ng/ml) or the HPD + cortisol group (5.6 +/- 1.9 ng/ml). We have demonstrated that there is a strong hypothalamic drive to prolactin synthesis and secretion in the fetus and that cortisol does not act directly at the fetal pituitary to stimulate prolactin synthesis and secretion in late gestation.
出生前催乳素合成与分泌的神经内分泌控制机制尚未完全明确。我们测定了妊娠最后15天内胎羊垂体前叶催乳素mRNA水平的变化(孕期足月为147±3天)。我们还研究了手术切断胎羊下丘脑与垂体(HPD),以及在此基础上长期输注皮质醇对妊娠晚期胎羊垂体催乳素mRNA水平和血浆催乳素浓度的影响。从一系列妊娠晚期的胎羊(130 - 134天,n = 6;135 - 140天,n = 6;141 - 145天,n = 6)收集垂体前叶,测定催乳素mRNA水平。在妊娠105 - 115天对10只胎羊进行HPD手术,并以5只完整胎羊作为对照。在HPD组中,从妊娠134 - 136天起,5天内分别输注生理盐水(HPD + 生理盐水组,n = 5)或皮质醇(3.5mg/24h)(HPD + 皮质醇组,n = 5)。胎羊垂体中催乳素mRNA与18S rRNA的比值在130 - 134天(0.46±0.08,n = 6)到135 - 140天(1.27±0.17,n = 6)之间有所增加,妊娠141天后维持该水平(1.27±0.11,n = 6)。完整胎羊(1.41±0.16,n = 4)的催乳素mRNA与18S rRNA平均比值显著高于HPD胎羊(无论是输注生理盐水后,0.54±0.14,n = 4;还是输注皮质醇后,0.74±0.24,n = 5)(P < 0.05)。完整组的血浆催乳素平均浓度(28.3±3.9ng/ml)也高于HPD + 生理盐水组(8.0±3.3ng/ml)或HPD + 皮质醇组(5.6±1.9ng/ml)。我们证明,胎儿体内存在强大的下丘脑驱动来促进催乳素的合成与分泌,并且在妊娠晚期,皮质醇并不直接作用于胎儿垂体来刺激催乳素的合成与分泌。