Bagatell C J, Matsumoto A M, Christensen R B, Rivier J E, Bremner W J
Medical Service, Seattle Veterans Affairs Medical Center, Washington.
J Clin Endocrinol Metab. 1993 Aug;77(2):427-32. doi: 10.1210/jcem.77.2.8345047.
Efforts to develop a hormonal contraceptive regimen for men have focused on administration of testosterone (T), alone or together with other agents. Previous regimens have successfully induced azoospermia in only 50-70% of subjects, however. GnRH antagonists, alone or in combination with T, have been shown to induce azoospermia in a very high percentage of nonhuman primates. We tested the hypothesis that the addition of a GnRH antagonist to a high-dose T regimen would lead to a higher percentage of men developing azoospermia than would T alone. We administered the GnRH antagonist, Nal-Glu (100 micrograms/kg.day sc), plus T enanthate, 200 mg im weekly or placebo sc injections daily plus T enanthate, 200 mg im weekly, to separate groups of healthy men for 16-20 weeks. Seven of 10 men who received Nal-Glu plus T and 6 of 9 men who received T alone became azoospermic; gonadotropin levels were suppressed and T levels were increased similarly in both groups. There was a trend toward higher pretreatment gonadotropin levels and lower sperm counts in men who became azoospermic. Weight gain, development of acne, and increases in hematocrit and hemoglobin were similar in the two groups. In the majority of the men, sperm counts returned to the baseline levels within 4-5 months after treatment ended. We conclude that with the dosages of Nal-Glu and T we used in this study, the addition of GnRH antagonist to a high-dose T regimen does not increase the ability of T to suppress spermatogenesis in healthy men. Use of a higher dose of Nal-Glu, a lower dose of T, delaying the start of T replacement until several weeks after Nal-Glu injections are initiated, or prolonged hormonal administration might lead to a combination regimen that will suppress spermatogenesis more fully than does T alone.
开发男性激素避孕方案的努力主要集中在单独使用睾酮(T)或与其他药物联合使用。然而,以往的方案仅在50%至70%的受试者中成功诱导了无精子症。促性腺激素释放激素(GnRH)拮抗剂单独或与T联合使用,已被证明能在非常高比例的非人灵长类动物中诱导无精子症。我们测试了这样一个假设,即与单独使用T相比,在高剂量T方案中添加GnRH拮抗剂会使更多男性出现无精子症。我们将GnRH拮抗剂Nal-Glu(100微克/千克·天,皮下注射)加庚酸睾酮(每周200毫克,肌肉注射)或安慰剂(每日皮下注射)加庚酸睾酮(每周200毫克,肌肉注射)分别给予不同组的健康男性,持续16至20周。接受Nal-Glu加T的10名男性中有7名以及单独接受T的9名男性中有6名出现了无精子症;两组的促性腺激素水平均受到抑制,T水平升高情况相似。出现无精子症的男性在治疗前促性腺激素水平较高且精子计数较低,存在这种趋势。两组在体重增加、痤疮发展以及血细胞比容和血红蛋白升高方面情况相似。在大多数男性中,治疗结束后4至5个月内精子计数恢复到基线水平。我们得出结论,就本研究中使用的Nal-Glu和T的剂量而言,在高剂量T方案中添加GnRH拮抗剂并不会增强T抑制健康男性精子发生的能力。使用更高剂量的Nal-Glu、更低剂量的T、在开始注射Nal-Glu几周后再开始T替代治疗,或延长激素给药时间,可能会形成一种比单独使用T更能充分抑制精子发生的联合方案。