Wu F C, Butler G E, Kelnar C J, Stirling H F, Huhtaniemi I
Medical Research Council, Reproductive Biology, Unit, University Department of Child Life and Health, Edinburgh, Scotland.
J Clin Endocrinol Metab. 1991 Jun;72(6):1229-37. doi: 10.1210/jcem-72-6-1229.
To study the ontogeny of spontaneous pulsatile LH and FSH secretion before the onset of puberty, plasma LH and FSH were measured by an ultrasensitive time-resolved immunoflurometric assay in 16 boys and 6 girls, aged 6.5 +/- 0.2 yr (+/- SEM; range, 4.4-8.0) with short stature. Eight male patients with idiopathic hypogonadotropic hypogonadism (Kallmann's syndrome), aged 24.1 +/- 3.4 yr, were also investigated. Blood samples were withdrawn at 10- to 20-min intervals for 12 h from 2000-0800 h. Pituitary responsiveness was assessed by a standard iv LHRH challenge test. LH and/or FSH pulses were detectable in all but two prepubertal subjects. In boys, low amplitude LH (0.16 +/- 0.06 U/L) and FSH (0.19 +/- 0.03 U/L) pulses were detectable at mean frequencies of 2.19 +/- 0.37 and 2.13 +/- 0.46 pulses/12 h, respectively. In girls, low amplitude LH (0.29 +/- 0.18 U/L) pulses, but higher (P less than 0.05 compared to boys) amplitude FSH (1.62 +/- 1.05 U/L) pulses were observed at frequencies of 1.71 +/- 0.56 and 1.67 +/- 0.53 pulses/12 h, respectively. Mean FSH in prepubertal girls (1.95 +/- 0.88 U/L) was significantly (P less than 0.05) higher than that in boys (0.46 +/- 0.07 U/L), but mean LH was not different at 0.17 +/- 0.07 and 0.10 +/- 0.03 U/L, respectively. Patients with Kallmann's syndrome had mean LH and FSH levels indistinguishable from those of prepubertal boys. Nocturnal augmentation of pulsatile LH or FSH secretion was observed in 74% of children (71% in girls and 75% in boys), but in none of the eight patients with Kallmann's syndrome. A close temporal association was observed between sleep onset and the appearance of nocturnal pulsatile gonadotropin secretion. The FSH response to exogenous LHRH in prepubertal girls was significantly greater than that in patients with Kallmann's syndrome and prepubertal boys, but LH responses were not different. Our results show that pulsatile LH and FSH secretion occurs in the majority of boys and girls in midchildhood, with a robust association with nocturnal sleep onset. Between the ages of 4-8 yr, these low amplitude and low frequency pulses are unable to activate gonadal function. The regulation of FSH secretion in prepubertal girls appears to be different from that in prepubertal boys.(ABSTRACT TRUNCATED AT 400 WORDS)
为研究青春期开始前自发性促黄体生成素(LH)和促卵泡生成素(FSH)脉冲式分泌的个体发生情况,采用超灵敏时间分辨免疫荧光分析法,对16名年龄为6.5±0.2岁(±标准误;范围4.4 - 8.0岁)身材矮小的男孩和6名女孩以及8名年龄为24.1±3.4岁的特发性低促性腺激素性性腺功能减退(卡尔曼综合征)男性患者的血浆LH和FSH进行了测定。在20:00至08:00期间,每隔10 - 20分钟采集一次血样,共采集12小时。通过标准静脉注射促性腺激素释放激素(LHRH)激发试验评估垂体反应性。除两名青春期前受试者外,其他所有受试者均可检测到LH和/或FSH脉冲。在男孩中,可检测到低幅度的LH脉冲(0.16±0.06 U/L)和FSH脉冲(0.19±0.03 U/L),平均频率分别为2.19±0.37次/12小时和2.13±0.46次/12小时。在女孩中,可观察到低幅度的LH脉冲(0.29±0.18 U/L),但FSH脉冲幅度更高(与男孩相比P<0.05)(1.62±1.05 U/L),频率分别为1.71±0.56次/12小时和1.67±0.53次/12小时。青春期前女孩的平均FSH(1.95±0.88 U/L)显著高于男孩(0.46±0.07 U/L)(P<0.05),但平均LH无差异,分别为0.17±0.07 U/L和0.10±0.03 U/L。卡尔曼综合征患者的平均LH和FSH水平与青春期前男孩无差异。74%的儿童(女孩为71%,男孩为75%)观察到LH或FSH脉冲式分泌的夜间增强,但8名卡尔曼综合征患者均未观察到。睡眠开始与夜间脉冲式促性腺激素分泌的出现之间存在密切的时间关联。青春期前女孩对外源性LHRH的FSH反应显著大于卡尔曼综合征患者和青春期前男孩,但LH反应无差异。我们的结果表明,大多数儿童中期的男孩和女孩会出现LH和FSH的脉冲式分泌,且与夜间睡眠开始密切相关。在4 - 8岁之间,这些低幅度和低频脉冲无法激活性腺功能。青春期前女孩FSH分泌的调节似乎与青春期前男孩不同。(摘要截选至400字)