Mann D R, Gould K G, Smith M M, Duffey T, Collins D C
Department of Physiology, Morehouse School of Medicine, Atlanta, Georgia 30310.
J Clin Endocrinol Metab. 1987 Dec;65(6):1215-24. doi: 10.1210/jcem-65-6-1215.
We examined the effect of continuous sc infusion of a GnRH agonist (Ag) and testosterone (T) supplementation on spermatogenesis and the potential fertilizing capacity of sperm in 15 rhesus monkeys. The monkeys were divided into 3 groups of 5 animals each. Groups 1 and 2 received 25 micrograms/day Ag for 44 weeks. Group 2 also received T replacement therapy [sufficient to maintain serum T values within the normal range; 4-5 ng/mL (13.9-17.3 nmol/L)]. Group 3 received a low dose of the Ag (5 micrograms/day for 24 weeks and then 10 micrograms/day for 20 weeks) to prolong the oligospermic phase before the onset of azoospermia. In groups 1 and 3, there was an initial transient (1 week) rise in serum LH and T levels which then fell below pretreatment value where they remained throughout the treatment period. The serum LH and T levels were lower in the group treated with 25 micrograms/day Ag. Similar changes in serum LH levels occurred in group 2, but T supplementation maintained serum T in the physiological range. The decline in serum LH levels was associated with reduced sensitivity to GnRH, since the responses of serum LH and T to GnRH were either abolished or greatly reduced in the 2 groups treated with 25 micrograms/day Ag and were less than 50% of the pre-Ag responses in monkeys treated with 5-10 micrograms/day Ag. Four of five monkeys treated with 25 micrograms/day Ag alone became azoospermic within 21 weeks. All five animals receiving Ag and T supplementation became azoospermic (mean time to onset, 12.6 weeks). Four of five monkeys treated with 5-10 micrograms/day Ag also had azoospermic ejaculates during the late treatment and early recovery period. Sperm counts recovered to the pretreatment levels in most monkeys by 10 weeks of the recovery period. The quality of semen samples taken from oligospermic monkeys was greatly reduced. The percentage of motile and percentage of live sperm per ejaculate, the net negative surface charge on sperm, and the scores of sperm in the hamster oocyte penetration test were subnormal. T supplementation did not improve these measures of semen quality. Testicular biopsies taken at the end of the Ag administration period from monkeys given 25 micrograms/day Ag showed diffuse atrophy of the seminiferous tubules, which contained primarily Sertoli cells and a few spermatogonia and spermatocytes, but no spermatids. The tubular atrophy and the suppression of spermatogenesis did not appear to be influenced by T replacement.(ABSTRACT TRUNCATED AT 400 WORDS)
我们研究了连续皮下注射促性腺激素释放激素激动剂(Ag)和补充睾酮(T)对15只恒河猴精子发生及精子潜在受精能力的影响。将猴子分为3组,每组5只。第1组和第2组连续44周每天接受25微克Ag。第2组还接受T替代疗法[足以使血清T值维持在正常范围内;4 - 5纳克/毫升(13.9 - 17.3纳摩尔/升)]。第3组接受低剂量的Ag(前24周每天5微克,后20周每天10微克),以延长无精子症发生前的少精子期。在第1组和第3组中,血清促黄体生成素(LH)和T水平最初有短暂(1周)升高,随后降至治疗前水平以下,并在整个治疗期间维持在该水平。每天接受25微克Ag治疗的组中血清LH和T水平较低。第2组血清LH水平也有类似变化,但补充T使血清T维持在生理范围内。血清LH水平的下降与对GnRH的敏感性降低有关,因为在每天接受25微克Ag治疗的2组中,血清LH和T对GnRH的反应要么消失要么大大降低,而在每天接受5 - 10微克Ag治疗的猴子中,这些反应小于Ag治疗前反应的50%。单独接受每天25微克Ag治疗的5只猴子中有4只在21周内出现无精子症。所有接受Ag和T补充治疗的5只动物均出现无精子症(平均发病时间为12.6周)。每天接受5 - 10微克Ag治疗的5只猴子中有4只在治疗后期和恢复早期射精中也出现无精子症。在恢复期10周时,大多数猴子的精子计数恢复到治疗前水平。从少精子症猴子采集的精液样本质量大大降低。每次射精中活动精子的百分比、活精子的百分比、精子表面净负电荷以及仓鼠卵母细胞穿透试验中精子的得分均低于正常水平。补充T并未改善这些精液质量指标。在给予每天25微克Ag的猴子中,在Ag给药期结束时进行的睾丸活检显示生精小管弥漫性萎缩,其中主要包含支持细胞以及少数精原细胞和精母细胞,但无精子细胞。生精小管萎缩和精子发生的抑制似乎不受T替代的影响。(摘要截短至400字)