Williams R F, Gianfortoni J G, Hodgen G D
J Clin Endocrinol Metab. 1985 Jan;60(1):126-32. doi: 10.1210/jcem-60-1-126.
We evaluated the quantitative and temporal characteristics of the estrogen component of an estrogen-progesterone synergy, which can induce hyperprolactinemia in macaques. In Exp I, six groups of monkeys were treated for 2 weeks with various doses of estradiol benzoate (EB), which resulted in peripheral estradiol concentrations of 250-1500 pg/ml, followed by 2 weeks of combined estrogen and progesterone treatment. In each of the groups, regardless of the dosages of estradiol benzoate alone, PRL concentrations remained within normal limits (approximately 18 ng/ml). In contrast, during the subsequent period of combined EB and progesterone therapy, hyperprolactinemia developed. The resultant PRL concentrations were not dependent on the dose of EB administered. In Exp II, three groups of monkeys were treated with EB (25 micrograms/kg) alone for various intervals and subsequently with both EB and progesterone for 14 days. When initiation of progesterone therapy was preceded by a 9- or 6-day period of estrogen priming, PRL concentrations were significantly (P less than 0.05) elevated within 3-4 days; in contrast, when the EB and progesterone treatments were initiated simultaneously, 8 days elapsed before the PRL elevations were significant. In a third experiment, to determine whether decidualized endometrium accounted for the increased PRL levels following estrogen and progesterone treatment, a hysterectomized monkey was treated with EB followed by combined EB and progesterone treatment. The PRL response was not different from that of intact monkeys similarly treated. From these findings we conclude 1) that the estrogen-progesterone synergy promoting PRL secretion is not of endometrial origin; 2) that approximately 1 week of estrogen priming is required for progesterone to induce PRL secretion; 3) and that the mode of action of estrogen is not dose dependent, but, rather, is a threshold effect.
我们评估了雌激素 - 孕酮协同作用中雌激素成分的定量和时间特征,这种协同作用可在猕猴中诱发高催乳素血症。在实验一中,六组猴子接受了为期2周的不同剂量苯甲酸雌二醇(EB)治疗,外周雌二醇浓度达到250 - 1500 pg/ml,随后进行为期2周的雌激素和孕酮联合治疗。在每组中,无论单独使用苯甲酸雌二醇的剂量如何,催乳素(PRL)浓度均保持在正常范围内(约18 ng/ml)。相比之下,在随后的EB和孕酮联合治疗期间,出现了高催乳素血症。所产生的PRL浓度并不依赖于所给予的EB剂量。在实验二中,三组猴子单独接受不同时间间隔的EB(25微克/千克)治疗,随后同时接受EB和孕酮治疗14天。当在孕酮治疗开始前有9天或6天的雌激素预处理时,PRL浓度在3 - 4天内显著升高(P < 0.05);相比之下,当EB和孕酮治疗同时开始时,8天后PRL才显著升高。在第三个实验中,为了确定蜕膜化的子宫内膜是否是雌激素和孕酮治疗后PRL水平升高的原因,对一只子宫切除的猴子先进行EB治疗,然后进行EB和孕酮联合治疗。其PRL反应与同样治疗的完整猴子没有差异。从这些发现中我们得出以下结论:1)促进PRL分泌的雌激素 - 孕酮协同作用并非源于子宫内膜;2)孕酮诱导PRL分泌需要约1周的雌激素预处理;3)雌激素的作用方式不是剂量依赖性的,而是一种阈值效应。