Kelch R P, Kaplan S L, Ghumbach M M
J Clin Invest. 1973 May;52(5):1122-8. doi: 10.1172/JCI107278.
Clomiphene citrate, an "anti-estrogen" with mild estrogenic properties, inhibits rather than stimulates gonadotropin excretion in prepubertal and early pubertal children. These and other data suggest that the sensitivity of the hypothalamic-pituitary "gonadostat" decreases at the onset of puberty. To test this hypothesis further, the daily excretion of urinary follicle-stimulating hormone (FSH) and luteinizing hormone (LH) was determined in 19 children (5 "short normals" and 14 with isolated human growth hormone (HGH) deficiency) who were given ethinyl estradiol (EE) 1.4-14.7 mug/m(2) per day (2-10 mug/day) for 4 to 7 days. In addition, plasma and urinary gonadotropins and plasma estrogens were serially determined in two prepubertal females(with isolated HGH deficiency) given two injections (24 h apart) of estradiol benzoate, 10 mug/kg. FSH and LH concentrations in plasma and kaolin-acetone urinary concentrates and plasma 17beta-estradiol (E(2)) and estrone (E(1)) were measured by radioimmunoassays. 2-3 mug/m(2) per day of EE significantly suppressed urinary FSH (and LH when detected in the control period) in two out of six prepubertal children, while all doses >5 mug/m(2) per day suppressed urinary gonadotropins to undetectable levels in eight prepubertal subjects. In early to midpubertal subjects. 2-10 mug/m(2) per day of EE produced a slight suppression of urinary FSH, but failed to suppress to undetectable levels. Two subjects in late puberty (stage 4) did not suppress their urinary FSH while on 7 and 8.3 mug/m(2) per day. In both subjects treated with estradiol benzoate, plasma FSH promptly decreased after the first injection. Urinary FSH was suppressed to <0.1 IU/day on day 2 and urinary and plasma gonadotropins remained suppressed for the duration of the study (3 days). Plasma E(2) and E(1) rose from prepubertal values to peak concentrations of 150 to 250 pg/ml (E(2)), and 50 and 100 pg/ml (E(1)) at approximately 36 h. We conclude that the hypothalamic-pituitary-gonadal axis is operative in the prepubertal child and that the sensitivity of the hypothalamic-pituitary center(s) which control the secretion of FSH and LH decreases at the onset of puberty in man.
枸橼酸氯米芬是一种具有轻度雌激素特性的“抗雌激素”药物,它抑制而非刺激青春期前和青春期早期儿童的促性腺激素分泌。这些及其他数据表明,下丘脑 - 垂体“性腺调节机制”在青春期开始时敏感性降低。为进一步验证这一假设,对19名儿童(5名“正常偏矮”儿童和14名单纯生长激素(HGH)缺乏儿童)进行了研究,这些儿童每天接受1.4 - 14.7μg/m²(2 - 10μg/天)的乙炔雌二醇(EE),持续4至7天,同时测定其每日尿促卵泡生成素(FSH)和促黄体生成素(LH)的排泄量。此外,对两名青春期前女性(单纯HGH缺乏)进行了研究,她们每隔24小时注射10μg/kg的苯甲酸雌二醇,连续注射两次,同时连续测定血浆和尿促性腺激素以及血浆雌激素水平。采用放射免疫分析法测定血浆和高岭土 - 丙酮尿浓缩物中的FSH和LH浓度以及血浆17β - 雌二醇(E₂)和雌酮(E₁)水平。在6名青春期前儿童中,有2名儿童每天给予2 - 3μg/m²的EE可显著抑制尿FSH(以及在对照期检测到的LH),而在8名青春期前受试者中,所有每日剂量>5μg/m²的EE均可将尿促性腺激素抑制至检测不到的水平。在青春期早期至中期的受试者中,每天给予2 - 10μg/m²的EE可使尿FSH略有抑制,但未能抑制至检测不到的水平。两名青春期后期(4期)受试者在每天给予7和8.3μg/m²的EE时,尿FSH未被抑制。在两名接受苯甲酸雌二醇治疗的受试者中,首次注射后血浆FSH迅速下降。第2天时尿FSH被抑制至<0.1IU/天,在研究期间(3天)尿和血浆促性腺激素一直处于被抑制状态。血浆E₂和E₁从青春期前水平升至峰值浓度,E₂约为150至250pg/ml,E₁约为50至100pg/ml,时间约为36小时。我们得出结论,下丘脑 - 垂体 - 性腺轴在青春期前儿童中就已发挥作用,并且在人类青春期开始时,控制FSH和LH分泌的下丘脑 - 垂体中心的敏感性降低。