Urbanski H F, Pickle R L, Ramirez V D
Division of Neuroscience, Oregon Regional Primate Research Center, Beaverton 97006.
Endocrinology. 1988 Jul;123(1):413-9. doi: 10.1210/endo-123-1-413.
In the present study two recently developed techniques have been combined to enable the simultaneous in vivo determination of pulsatile release of GnRH, LH, and FSH in the orchidectomized rat. The first of these techniques involves the implantation of two vascular catheters and collecting serial blood samples through one while simultaneously infusing a replacement blood mixture through the other; consequently, blood samples can be collected for an extended period of time, and detailed plasma LH and FSH release profiles can be established for individual animals. The second technique involves push-pull perfusion of the pituitary gland to determine changes in GnRH concentration as might be perceived by the gonadotropes. For each animal (n = 6), blood (150 microliters) and push-pull perfusate (200 microliters) samples were collected at 5- and 10-min intervals, respectively, for approximately 6 h, and the hormone release profiles were determined by RIA. All of the rats showed a clear pulsatile release pattern for GnRH, LH, and FSH. Moreover, the interpulse interval was remarkably similar for each of these hormones (36.9, 41.5, and 43.5 min, respectively, as determined by PULSAR). The percentage of GnRH pulses associated with a gonadotropin pulse was 72% for LH and 76% for FSH; only 14% of the pulses were silent for both gonadotropins. These results demonstrate that in the orchidectomized rat the pulsatile pattern of GnRH release is reflected in the pulsatile pattern of not only LH but also FSH. They may, therefore, be construed to support the concept that the pulsatile secretion of both gonadotropins is primarily orchestrated by a single hypothalamic releasing hormone. Alternatively, if two separate hypothalamic releasing hormones do indeed exist (LHRH and FSH-releasing hormone), it would appear that in the orchidectomized rat their episodic release is tightly coupled to the same hypothalamic pulse generator.
在本研究中,两种最近开发的技术被结合起来,以在去势大鼠体内同时测定促性腺激素释放激素(GnRH)、促黄体生成素(LH)和促卵泡生成素(FSH)的脉冲式释放。其中第一种技术包括植入两根血管导管,通过一根导管采集系列血样,同时通过另一根导管输注替代血液混合物;因此,可以长时间采集血样,并为每只动物建立详细的血浆LH和FSH释放曲线。第二种技术涉及对垂体进行推挽式灌注,以确定促性腺激素细胞所感知的GnRH浓度变化。对于每只动物(n = 6),分别以5分钟和10分钟的间隔采集血液样本(150微升)和推挽式灌注液样本(200微升),持续约6小时,并通过放射免疫分析(RIA)测定激素释放曲线。所有大鼠的GnRH、LH和FSH均呈现明显的脉冲式释放模式。此外,这些激素各自的脉冲间期非常相似(分别由PULSAR测定为36.9分钟、41.5分钟和43.5分钟)。与促性腺激素脉冲相关的GnRH脉冲百分比,LH为72%,FSH为76%;两种促性腺激素均无脉冲的情况仅占14%。这些结果表明,在去势大鼠中,GnRH释放的脉冲模式不仅反映在LH的脉冲模式中,也反映在FSH的脉冲模式中。因此,这些结果可以被解释为支持这样一种观点,即两种促性腺激素的脉冲式分泌主要由单一的下丘脑释放激素协调。或者,如果确实存在两种不同的下丘脑释放激素(促黄体生成素释放激素和促卵泡生成素释放激素),那么在去势大鼠中,它们的间歇性释放似乎与同一个下丘脑脉冲发生器紧密耦合。