Heber D, Swerdloff R S
Endocrinology. 1981 May;108(5):2019-21. doi: 10.1210/endo-108-5-2019.
We recently demonstrated that superactive gonadotropin-releasing hormone (GnRH) analogs and testosterone synergistically suppress gonadotropin secretion in castrate rats. We proposed that these two classes of agents used in combination would lead to enhanced suppression of spermatogenesis by synergistically inhibiting gonadotropin secretion. This hypothesis was tested in the present study in which synergistic inhibition of spermatogenesis was produced by combined analog and testosterone treatment. The mechanism of the synergistic action observed differed from that hypothesized in that the analog had both primary inhibitory actions directly on the testis and effects at a pituitary level. The addition of testosterone to the regimen further inhibited spermatogenesis by decreasing the secretion of gonadotropins thereby attenuating the compensatory rise in LH and FSH secretion expected with direct analog inhibition of the testis. These studies demonstrate the potential of combined GnRH analog and testosterone administration as a male contraceptive agent and indicate the complexity of their synergistic interactions.
我们最近证明,超活性促性腺激素释放激素(GnRH)类似物和睾酮可协同抑制去势大鼠的促性腺激素分泌。我们提出,这两类药物联合使用将通过协同抑制促性腺激素分泌,从而增强对精子发生的抑制作用。本研究对这一假设进行了验证,通过联合使用类似物和睾酮处理产生对精子发生的协同抑制作用。观察到的协同作用机制与假设不同,因为类似物不仅对睾丸有直接的主要抑制作用,还对垂体水平有影响。在该方案中添加睾酮可通过减少促性腺激素的分泌进一步抑制精子发生,从而减弱预期因类似物直接抑制睾丸而导致的LH和FSH分泌的代偿性升高。这些研究证明了联合使用GnRH类似物和睾酮作为男性避孕药物的潜力,并表明了它们协同相互作用的复杂性。