Döcke F, Dörner G
Zentralbl Gynakol. 1979;101(17):1082-8.
Experiments were performed in rats to study the role played by ovarian estrogens, the hypothalamus, the medicortical amygdala, and the ventral hipopcampus in the neurohormonal control of female sexual maturation. The results obtained demonstrated that the ovulation-inducing effect of a single administration of estradiol benzoate (EB) to immature female rats is not tantamount to the induction of precocious puberty. Long-term treatment with very low doses of EB, however, can accelerate sexual maturation, although it was established that the endogenous ovarian estrogen secretion during prepuberal life is not essential for the maturation of the cyclic ovarian function. Implantation of very low quantities of EB into the mediobasal hypothalamus of ovariectomized immature and postpuberal female rats revealed that the hypothalamic sensitivity to the LH-inhibiting effect of estrogen exhibits a gradual decrease that begins some days prior to the onset of puberty. It may be responsible for a temporary elevation of the LH level in the blood triggering final maturation of the ovarian follicles and an increase of estrogen secretion. - Studies on the influence of the limbic system on female sexual maturation lead to the following conclusions: 1. The mediocortical amygdala has an essential function in the maturation of the positive estrogen feedback. 2. An LH-inhibiting activity not related to the negative estrogen feedback is exerted by this nuclear region during critical periods of sexual maturation. It may form an additional protective mechanism against precocious stimulation of the ovaries. 3. By means of its stimulatory action on growth hormone and FSH secretion, the ventral hippocampus may be involved, by cholinergic mechanisms, in the interrelationships between metabolism and the onset of female puberty. The results which suggest a significant role of the limbic system in the control of female sexual maturation will be discussed with regard to recent data obtained in girls and women.
在大鼠身上进行了实验,以研究卵巢雌激素、下丘脑、内侧皮质杏仁核和腹侧海马体在雌性性成熟的神经激素控制中所起的作用。获得的结果表明,对未成熟雌性大鼠单次给予苯甲酸雌二醇(EB)的促排卵作用并不等同于诱导性早熟。然而,用极低剂量的EB进行长期治疗可以加速性成熟,尽管已确定青春期前内源性卵巢雌激素分泌对于周期性卵巢功能的成熟并非必不可少。将极少量的EB植入去卵巢的未成熟和青春期后雌性大鼠的中基底下丘脑,结果显示下丘脑对雌激素抑制促黄体生成素(LH)作用的敏感性在青春期开始前几天就开始逐渐降低。这可能是导致血液中LH水平暂时升高的原因,从而触发卵巢卵泡的最终成熟和雌激素分泌增加。 - 关于边缘系统对雌性性成熟影响的研究得出以下结论:1. 内侧皮质杏仁核在雌激素正反馈的成熟中具有重要作用。2. 在性成熟的关键时期,该核区域会发挥一种与雌激素负反馈无关的LH抑制活性。它可能形成一种额外的保护机制,防止卵巢过早受到刺激。3. 通过对生长激素和促卵泡生成素(FSH)分泌的刺激作用,腹侧海马体可能通过胆碱能机制参与代谢与女性青春期开始之间的相互关系。将结合最近在女孩和女性中获得的数据,讨论表明边缘系统在雌性性成熟控制中起重要作用的结果。