Döcke F, Dörner G
Zentralbl Gynakol. 1978;100(1):3-12.
To study the mode of action of oestrogen in female sexual maturation, prepubertal female rats were treated in different ways with oestradiol benzoate (OB). Using an improved implantation method, former findings on a hypophysial site of oestrogen action in the positive feedback (Hohlweg effect) were confirmed. A single s.c. injection or intrahypophysial implantation of OB at 25 or 26 days of age induced precocious vaginal opening (VO) and one ovulation, but the subsequent ovarian cycle was significantly prolonged, so that the first spontaneous ovulation occurred only at the normal time of the onset of puberty. Further studies demonstrated that the sensitivity to the ovulation-inducing effect of oestrogen increases as the rats approach the age of puberty, and that the first pubertal ovulation can be suppressed by intrahypophysial, but not by intrahypothalamic implantation of progestereone. The conclusion is drawn that the precocious induction of one ovulation via the Hohlweg effect is not tantamount to an advancement of puberty. The results furthermore suggest that the positive oestrogen feedback forms the basis for the first pubertal ovulation as it does with regard to later cyclic ovulations. True acceleration of sexual maturation was achieved by daily injections of 0,05 microgram OB/100 g b.w. from 5 days of age to VO. In contrast to findings obtained by other authors in Sprague-Dawley rats, a shortened OB treatment from 26 days of age to VO was not effective in advancing the onset of puberty unless the rats had additionally been injected with OB from 5 to 10 days of age. A final experiment demonstrated that the first ovarian cycle was not prolonged after neonatal ovariectomy and implantation of ovaries at 24, 28 or 32 days of age. Thus, maturation of the neurohormonal mechanisms that are responsible for the cyclic ovarian function continues during the prepubertal development in the absence of ovarian steroids.
为研究雌激素在雌性性成熟中的作用方式,对青春期前雌性大鼠用苯甲酸雌二醇(OB)进行不同方式的处理。采用改良的植入方法,证实了先前关于雌激素在正反馈中作用于垂体部位(霍尔韦格效应)的研究结果。在25或26日龄时单次皮下注射或垂体内植入OB可诱导早熟阴道开口(VO)和一次排卵,但随后的卵巢周期明显延长,以至于第一次自发排卵仅在青春期开始的正常时间出现。进一步研究表明,随着大鼠接近青春期,对雌激素诱导排卵作用的敏感性增加,并且第一次青春期排卵可被垂体内植入孕酮抑制,但不能被下丘脑内植入孕酮抑制。得出的结论是,通过霍尔韦格效应早熟诱导一次排卵并不等同于青春期提前。结果还表明,雌激素正反馈是第一次青春期排卵的基础,就像其对后期周期性排卵一样。通过从5日龄至VO每日注射0.05微克OB/100克体重实现了性成熟的真正加速。与其他作者在斯普拉格-道利大鼠中获得的结果相反,从26日龄至VO缩短OB治疗在提前青春期开始方面无效,除非大鼠在5至10日龄时额外注射了OB。最后一项实验表明,新生卵巢切除并在24、28或32日龄植入卵巢后,第一个卵巢周期并未延长。因此,在没有卵巢类固醇的情况下,负责卵巢周期性功能的神经激素机制在青春期前发育过程中持续成熟。