Colombani-Vidal M, Barnea A
Neuroendocrinology. 1985 Dec;41(6):454-61. doi: 10.1159/000124219.
We have previously shown that chelated copper stimulates the release of luteinizing hormone releasing hormone (LHRH) from explants of the median eminence area (MEA) incubated under in vitro conditions and that this stimulation involves a ligand-specific interaction. In this study, we addressed the question: do testicular steroids regulate the secretory response of LHRH neurons to copper? MEA, obtained from immature, mature, immature castrated and sham-operated rats, were incubated in the presence of various concentrations of copper for 15 min and then in the absence of copper for an additional period of 30 min. We noted that after a lag period of 5 min of incubation, the rate of LHRH release increased in a linear fashion for a period of 15 min. In addition, the rate of LHRH release as well as the rate at which LHRH release was accelerated were saturable functions of the concentration of copper. When incubation was carried out in the presence of a nonsaturating concentration of copper (50 microM), the fractional amount (percent of the total MEA content) of LHRH released from the MEA of castrated rats was significantly (p less than 0.001) lower than that from sham-operated rats; stimulated release being 0.9% and 1.4%, respectively. Similarly, copper-stimulated release from the MEA of immature rats was lower than that from the MEA of mature rats. However, when incubation was carried out in the presence of saturating concentrations of copper (100 or 200 microM), the percentage of stimulated release from the MEA of castrated rats was similar to that of sham-operated rats and significantly lower than that of mature and sham-operated rats, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
我们之前已经表明,螯合铜能刺激体外培养的正中隆起区(MEA)外植体释放促黄体生成激素释放激素(LHRH),且这种刺激涉及配体特异性相互作用。在本研究中,我们探讨了以下问题:睾丸类固醇是否调节LHRH神经元对铜的分泌反应?从未成熟、成熟、未成熟去势和假手术大鼠获取MEA,在不同浓度的铜存在下孵育15分钟,然后在无铜条件下再孵育30分钟。我们注意到,孵育5分钟的延迟期后,LHRH释放速率在15分钟内呈线性增加。此外,LHRH释放速率以及LHRH释放加速的速率是铜浓度的饱和函数。当在非饱和浓度的铜(50微摩尔)存在下进行孵育时,去势大鼠MEA释放的LHRH的分数含量(占MEA总含量的百分比)显著低于假手术大鼠(p<0.001);刺激释放分别为0.9%和1.4%。同样,未成熟大鼠MEA的铜刺激释放低于成熟大鼠MEA。然而,当在饱和浓度的铜(100或200微摩尔)存在下进行孵育时,去势大鼠MEA的刺激释放百分比与假手术大鼠相似,且分别显著低于成熟大鼠和假手术大鼠。(摘要截短于250字)