Matsumoto A M, Karpas A E, Southworth M B, Dorsa D M, Bremner W J
Endocrinology. 1986 Jul;119(1):362-9. doi: 10.1210/endo-119-1-362.
During sexual development in the male rat, serum testosterone (T) levels increase markedly at 45-60 days of age. At the time of the pubertal rise in T levels, activation of the hypothalamic-pituitary axis is difficult to demonstrate, since there is little change in serum LH levels and a decrease in serum FSH levels. We determined whether experimental maintenance of stable pubertal T levels in these animals as they passed through the normal age of puberty would allow demonstration of a major increase in serum gonadotropin levels. At 14-15 days of age, male rats were castrated and outfitted with either T-containing or empty Silastic capsules. Another group of rats was left intact and outfitted with empty capsules. At various times between 29 and 58 days of age, blood was drawn for measurement of serum LH, FSH, and T levels. In the T-implanted castrated rats, serum T levels were comparable to those in midpubertal intact rats, without significant differences among age groups. In this setting of stable T levels, serum LH and FSH were suppressed to levels at or below those in pubertal intact rats until 51 days of age, when they increased significantly into the untreated castrate range. In contrast, untreated castrate animals demonstrated markedly reduced serum T and elevated LH and FSH levels that did not change significantly throughout the entire study. In intact rats, serum T levels were stable until 58 days of age, when they increased over 2-fold; serum LH levels did not change significantly with age, and serum FSH levels decreased significantly by 54 days of age. A separate group of rats was castrated and outfitted with T-containing Silastic capsules at 21 days of age. In these animals, there were significant increases in hypothalamic LHRH, norepinephrine (NE), and dopamine levels and NE turnover rate at 56 compared to 36 days of age. We conclude that stable pubertal levels of T are able to suppress gonadotropin levels in castrated rats until the normal age of puberty, at which time LH and FSH levels increase markedly. This decrease in sensitivity of the hypothalamic-pituitary axis to T negative feedback at puberty is accompanied by increases in hypothalamic LHRH, NE, and dopamine levels and NE turnover rate. These results provide direct evidence for activation of the central nervous system-pituitary mechanism regulating gonadotropin secretion at puberty in the male rat.(ABSTRACT TRUNCATED AT 400 WORDS)
在雄性大鼠的性发育过程中,血清睾酮(T)水平在45至60日龄时显著升高。在T水平出现青春期上升时,下丘脑 - 垂体轴的激活难以证明,因为血清促黄体生成素(LH)水平变化不大,而血清促卵泡生成素(FSH)水平下降。我们确定,在这些动物正常进入青春期时,通过实验维持稳定的青春期T水平是否能证明血清促性腺激素水平会大幅升高。14至15日龄时,对雄性大鼠进行阉割,并植入含T或不含T的硅橡胶胶囊。另一组大鼠不做处理并植入不含T的胶囊。在29至58日龄的不同时间点采集血液,检测血清LH、FSH和T水平。在植入T的阉割大鼠中,血清T水平与青春期中期未阉割大鼠相当,各年龄组之间无显著差异。在T水平稳定的情况下,血清LH和FSH被抑制至青春期未阉割大鼠的水平或更低,直到51日龄时显著升高至未处理的阉割大鼠范围。相比之下,未处理的阉割动物血清T水平显著降低,LH和FSH水平升高,且在整个研究过程中无显著变化。在未阉割大鼠中,血清T水平直到58日龄时都保持稳定,之后升高超过2倍;血清LH水平随年龄无显著变化,血清FSH水平在54日龄时显著下降。另一组大鼠在21日龄时进行阉割并植入含T的硅橡胶胶囊。与36日龄相比,这些动物在56日龄时下丘脑促性腺激素释放激素(LHRH)、去甲肾上腺素(NE)和多巴胺水平以及NE周转率均显著增加。我们得出结论,稳定的青春期T水平能够抑制阉割大鼠的促性腺激素水平,直到正常青春期年龄,此时LH和FSH水平显著升高。青春期下丘脑 - 垂体轴对T负反馈敏感性的降低伴随着下丘脑LHRH、NE和多巴胺水平以及NE周转率的增加。这些结果为雄性大鼠青春期调节促性腺激素分泌的中枢神经系统 - 垂体机制的激活提供了直接证据。(摘要截断于400字)