Harris Glenn C, Levine Jon E
Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA.
Endocrinology. 2003 Jan;144(1):163-71. doi: 10.1210/en.2002-220767.
A microdialysis technique was used in male rats to directly assess the postulate that pubertal maturation is associated with accelerated GnRH pulsatility. Juvenile male rats, postnatal d 43 or 45 (n = 4) were stereotaxically fitted with guide cannulas directed toward the lateral median eminence, and repeated microdialysis experiments were conducted over 4-6 d. In each session, samples were collected continuously over 12 h (0900-2100 h) at 5-min intervals Results from individual peripubertal animals were pooled into two time bins for postnatal d 45-47 and 48-50, respectively, and GnRH characteristics were compared between the two epochs. The GnRH pulse frequency and mean GnRH concentration were significantly elevated at 48-50 d compared with 45-47 d. The GnRH pulsatility characteristics for 45-47 d vs. 48-50 d were as follows: pulse frequency, 0.74 +/- 0.16 vs. 1.79 +/- 0.19 pulses/h (P < 0.05); pulse amplitude, 254.1 +/- 22.3 vs. 347.2 +/- 15.8 deltapg/ml (difference in value from trough to peak); and mean release, 0.55 +/- 0.03 vs. 2.04 +/- 0.04 pg/5 min (P < 0.05). An additional two rats were dialyzed only once on postnatal d 50 to assess the effects of repeated sampling; the GnRH pulse characteristics in these animals were similar to those in rats sampled for a third or fourth time on postnatal d 48-50. To further assess the possible effects of repeated sampling on GnRH release profiles, a group of adult male rats (postnatal d 95-105; n = 3) was also dialyzed on four consecutive days. In these rats no significant alteration in GnRH pulse generator activity was observed over the four sessions. Moreover, the increase in GnRH pulse frequency observed in the peripubertal rats was found to be sustained in adult animals. To better understand the temporal relationship of GnRH pulse generator activity to reproductive maturation, groups of male rats were killed from postnatal d 45-56 along with an adult group at 95-105 d (n = 5/group) and examined for physiological signs of reproductive development. Gradual increases in serum levels of LH and testosterone and decreases in FSH and inhibin B were seen from postnatal d 45-56 to adulthood. Mature spermatozoa were found in the vas deferens by postnatal d 53. Our results demonstrate that in the late juvenile stage of male rat development, GnRH pulse generator activity is gradually accelerated over the course of consecutive days. This acceleration occurs over a period during which serum LH and testosterone are rising to adult levels, and it precedes the presence of mature spermatozoa in the vas deferens by 3 d. Our observations provide direct support for the hypothesis that an acceleration of GnRH pulsatility is the critical neural stimulus for the initiation of pubertal maturation in males. The peripheral and central cues that prompt the pubertal activation of the GnRH pulse generator remain to be characterized.
采用微透析技术对雄性大鼠进行研究,以直接验证青春期成熟与促性腺激素释放激素(GnRH)脉冲频率加快有关这一假设。出生后第43天或45天的幼年雄性大鼠(n = 4)通过立体定位法在其朝向外侧正中隆起处植入引导套管,并在4 - 6天内进行重复微透析实验。在每次实验中,于12小时内(09:00 - 21:00)每隔5分钟连续采集样本。将青春期前个体动物的实验结果分别汇总到出生后第45 - 47天和48 - 50天这两个时间段,并比较这两个时期的GnRH特征。与45 - 47天相比,48 - 50天时GnRH脉冲频率和平均GnRH浓度显著升高。45 - 47天与48 - 50天的GnRH脉冲特征如下:脉冲频率,0.74±0.16次/小时对1.79±0.19次/小时(P < 0.05);脉冲幅度,254.1±22.3对347.2±15.8Δpg/ml(谷值到峰值的差值);平均释放量,0.55±0.03对2.04±0.04 pg/5分钟(P < 0.05)。另外两只大鼠在出生后第50天仅进行了一次透析,以评估重复采样的影响;这些动物的GnRH脉冲特征与在出生后第48 - 50天进行第三次或第四次采样的大鼠相似。为进一步评估重复采样对GnRH释放曲线的可能影响,一组成年雄性大鼠(出生后第95 - 105天;n = 3)也连续四天进行透析。在这些大鼠中,四个实验阶段未观察到GnRH脉冲发生器活性有显著变化。此外,在青春期前大鼠中观察到的GnRH脉冲频率增加在成年动物中持续存在。为更好地理解GnRH脉冲发生器活性与生殖成熟的时间关系,在出生后第45 - 56天处死几组雄性大鼠,并在95 - 105天处死一组成年大鼠(每组n = 5),检查其生殖发育的生理迹象。从出生后第45 - 56天到成年期,血清促黄体生成素(LH)和睾酮水平逐渐升高,促卵泡生成素(FSH)和抑制素B水平逐渐降低。到出生后第53天,在输精管中发现了成熟精子。我们的结果表明,在雄性大鼠发育的幼年晚期,GnRH脉冲发生器活性在连续数天内逐渐加快。这种加快发生在血清LH和睾酮水平上升至成年水平的时期,且在输精管中出现成熟精子前3天发生。我们的观察结果为GnRH脉冲频率加快是男性青春期成熟启动的关键神经刺激这一假设提供了直接支持。促使GnRH脉冲发生器青春期激活的外周和中枢信号仍有待确定。