Weinbauer G F, Respondek M, Themann H, Nieschlag E
Max Planck Clinical Research Unit for Reproductive Medicine, University of Münster, Federal Republic of Germany.
J Androl. 1987 Sep-Oct;8(5):319-29. doi: 10.1002/j.1939-4640.1987.tb00970.x.
The present investigation evaluates the long-term effects of GnRH agonist treatment on testicular histology, sperm production and the subsequent recovery of these parameters. Four adult rhesus monkeys (M. mulatta) were treated with the GnRH agonist nafarelin (D-Nal(2)6-GnRH), released from i.m.--injected poly-D,L-lactic-co-glycolide microspheres for 20 months. Monthly injection of the GnRH agonist preparation uniformly suppressed serum levels of bioactive LH and testosterone. The size of the testis was reduced to about 30% of pretreatment. Sperm counts were suppressed to azoospermia for a total period of 53 and 77 weeks, respectively, in two monkeys and the other two animals were extremely oligozoospermic. Evaluation of testicular biopsy material after 6, 12 and 20 months of treatment revealed decreased seminiferous tubule diameter, spermatogenic disruption at the level of spermatogonia or spermatocytes, accumulation of lipid droplets and secondary lysosomes in the Sertoli cell cytoplasm, and increased thickness of the tubular wall compared with pretreatment histology. Electron microscopic examination revealed that the increased wall thickness was due to an enlargement of the inner collagen layer. No evidence of fibrosis or calcification could be obtained. Leydig cells were atrophic. Serum hormones, testis size and sperm counts returned to pretreatment values within 5 to 8, 13 to 16, and 18 weeks, respectively, after termination of treatment. Testicular histology, assessed 8 months after cessation of treatment, was indistinguishable from pretreatment. It is concluded that GnRH agonist-containing microspheres are a feasible modality for sustained administration of GnRH agonists and GnRH agonist-induced suppression of pituitary and testicular function is reversible following withdrawal of treatment. Thus, GnRH agonists may have a potential for regulation of male fertility and, presumably, also for treatment of precocious puberty.
本研究评估了促性腺激素释放激素(GnRH)激动剂治疗对睾丸组织学、精子生成以及这些参数随后恢复情况的长期影响。四只成年恒河猴(猕猴)接受了从肌肉注射的聚-D,L-乳酸-共-乙醇酸微球中释放的GnRH激动剂那法瑞林(D-Nal(2)6-GnRH)治疗,为期20个月。每月注射GnRH激动剂制剂可均匀抑制生物活性促黄体生成素(LH)和睾酮的血清水平。睾丸大小降至治疗前的约30%。在两只猴子中,精子计数分别被抑制至无精子症达53周和77周,另外两只动物则为极度少精子症。治疗6个月、12个月和20个月后对睾丸活检材料的评估显示,与治疗前组织学相比,生精小管直径减小,精原细胞或精母细胞水平的生精破坏,支持细胞胞质中脂滴和次级溶酶体积累,以及管壁厚度增加。电子显微镜检查显示管壁厚度增加是由于内部胶原层增大。未发现纤维化或钙化迹象。睾丸间质细胞萎缩。治疗终止后,血清激素、睾丸大小和精子计数分别在5至8周、13至16周和18周内恢复到治疗前值。治疗停止8个月后评估的睾丸组织学与治疗前无差异。结论是,含GnRH激动剂的微球是持续给予GnRH激动剂的一种可行方式,并且治疗停止后GnRH激动剂诱导的垂体和睾丸功能抑制是可逆的。因此,GnRH激动剂可能具有调节男性生育能力的潜力,大概也可用于治疗性早熟。