Mann D R, Gould K G, Collins D C, Wallen K
Department of Physiology, Morehouse School of Medicine, Atlanta, Georgia 30310.
J Clin Endocrinol Metab. 1989 Mar;68(3):600-7. doi: 10.1210/jcem-68-3-600.
The objective of this study was to examine the effect of blockade of neonatal activation of the pituitary-testicular axis, using a GnRH agonist, on sexual development in male rhesus monkeys. Monkeys were treated with either a GnRH agonist (10 micrograms/day; n = 8) or vehicle (n = 9) for 112 days using osmotic minipumps beginning at 10-13 days of age. In control monkeys serum LH and testosterone concentrations during the first 3 postnatal months were similar to those in adults; they then declined to very low levels. GnRH agonist administration caused an immediate and precipitous decline in serum LH and testosterone concentrations to very low levels, and both remained low throughout the rest of the agonist administration period. Neither group had any significant elevation in serum LH or testosterone concentrations during the next 2 yr. In the control monkeys serum LH and testosterone began to rise during the third year, with a rapid increase occurring during the fall coincident with the breeding season. This peripubertal rise of LH and testosterone secretion was associated with rapid enlargement of the testes and the appearance of sperm in ejaculates. The monkeys who had received GnRH agonist had subnormal serum LH and testosterone increases, and testicular enlargement was also attenuated compared to that in the control animals during the third year of life. Semen samples were recovered from only 50% of the GnRH agonist-treated monkeys during this period, and the sperm count per ejaculate was suppressed. The serum LH responses of the GnRH agonist-treated monkeys to an iv bolus dose of GnRH (5 micrograms/kg BW) during the third year were normal. These results suggest that the induction of reversible hypogonadotropin-hypogonadism in neonatal male monkeys alters subsequent testicular development and peripubertal endocrine changes. Thus, neonatal activation of the pituitary-testicular axis may be a critical developmental event in the process of sexual development in male primates.
本研究的目的是使用促性腺激素释放激素(GnRH)激动剂,研究阻断新生雄性恒河猴垂体-睾丸轴激活对其性发育的影响。从10-13日龄开始,使用渗透微型泵对猴子进行112天的治疗,一组给予GnRH激动剂(10微克/天;n = 8),另一组给予赋形剂(n = 9)。在对照猴子中,出生后前3个月血清促黄体生成素(LH)和睾酮浓度与成年猴子相似;随后它们降至非常低的水平。给予GnRH激动剂导致血清LH和睾酮浓度立即急剧下降至非常低的水平,并且在激动剂给药期的其余时间内两者均保持在低水平。在接下来的2年中,两组猴子的血清LH或睾酮浓度均未出现任何显著升高。在对照猴子中,血清LH和睾酮在第三年开始升高,在秋季与繁殖季节一致时迅速增加。这种青春期前LH和睾酮分泌的增加与睾丸迅速增大以及射精中出现精子有关。接受GnRH激动剂治疗的猴子在第三年血清LH和睾酮增加低于正常水平,并且与对照动物相比,睾丸增大也减弱。在此期间,仅从50%接受GnRH激动剂治疗的猴子中采集到精液样本,并且每次射精的精子计数受到抑制。在第三年,接受GnRH激动剂治疗的猴子对静脉注射大剂量GnRH(5微克/千克体重)的血清LH反应正常。这些结果表明,新生雄性猴子中可逆性低促性腺激素性性腺功能减退的诱导会改变随后的睾丸发育和青春期前内分泌变化。因此,垂体-睾丸轴的新生激活可能是雄性灵长类动物性发育过程中的一个关键发育事件。