Sharpe R M, Fraser H M
J Reprod Fertil. 1980 Nov;60(2):359-68. doi: 10.1530/jrf.0.0600359.
Daily treatment of immature (30-day-old) male rats for 40 days with 50 ng of an agonist of LH-RH impaired normal development of Leydig cell function. This treatment partly or completely inhibited maturational increases in (1) the serum levels of testosterone, (2) seminal vesicle weight, (3) the in-vitro steroidogenic responsiveness of the testis, and (4) the in-vitro testicular binding of 125I-labelled hCG. In contrast, twice-weekly treatment of immature or adult rats with 50 ng LH-RH agonist had only minor effects on Leydig cell function, although hCG-binding was always significantly reduced. Testicular growth in immature rats was unaffected by daily injection of LH-RH agonist whereas twice-weekly treatment caused a small reduction in weight. None of the treatments had any major consistent effect on the pituitary or serum levels of gonadotrophins and prolactin, although daily treatment with the LH-RH agonist clearly reduced the responsiveness of the pituitary to the agonist, in terms of the amounts of LH and FSH released.
用50纳克促黄体生成素释放激素(LH-RH)激动剂对30日龄未成熟雄性大鼠进行为期40天的每日治疗,会损害睾丸间质细胞功能的正常发育。这种治疗部分或完全抑制了以下方面成熟过程中的增加:(1)血清睾酮水平;(2)精囊重量;(3)睾丸体外类固醇生成反应性;(4)125I标记的人绒毛膜促性腺激素(hCG)的体外睾丸结合。相比之下,用50纳克LH-RH激动剂对未成熟或成年大鼠进行每周两次的治疗,对睾丸间质细胞功能只有轻微影响,尽管hCG结合总是显著降低。未成熟大鼠的睾丸生长不受每日注射LH-RH激动剂的影响,而每周两次的治疗会导致体重略有减轻。尽管用LH-RH激动剂进行每日治疗明显降低了垂体对激动剂的反应性,即LH和FSH的释放量,但这些治疗对垂体或血清促性腺激素和催乳素水平均无任何主要的一致性影响。