Department of Physiology, Centre for Studies in Reproduction, School of Medicine, University of Maryland, Baltimore, Maryland 21201, USA.
J Neuroendocrinol. 1989 Aug 1;1(4):279-83. doi: 10.1111/j.1365-2826.1989.tb00116.x.
Abstract We examined the temporal changes in plasma luteinizing hormone (LH) levels, median eminence luteinizing hormone-releasing hormone (LHRH) concentrations and LHRH mRNA levels in estrogen-treated, ovariectomized rats with empty or antiestrogen- containing microcannulae stereotaxically implanted into the medial preoptic area. Neither treatment disrupted the negative feedback effects of estrogen on LH secretion, but antiestrogen (Keoxifene) blocked the afternoon LH surges. In rats exhibiting LH surges, median eminence LHRH concentrations were similar at 0800, 1200 and 1600 h, but they were significantly elevated by 2000 h. In contrast, no alterations in LHRH concentrations occurred in the Keoxifene-treated group. LHRH mRNA levels in control rats were significantly elevated at 1200, 1600 and 2000 h compared with 0800 h, but LHRH mRNA levels in Keoxifene-treated rats did not change significantly over the time period examined. When we compared treatment effects over time we saw that serum LH levels were significantly higher in control than Keoxifene-treated rats only at 1600 and 2000 h. Median eminence LHRH concentrations did not differ between treatment groups until 2000 h when control animals had significantly higher levels than those of Keoxifene-treated animals. LHRH mRNA levels in Keoxifene-treated rats were significantly higher than those of controls at 0800 hand significantly lower at 1600 h. No differences in LHRH mRNA levels were detected between groups at either 1200 h or 2000 h. In summary, although it was not clear on which neuronal system estrogen acted, depriving medial preoptic neurons of this steroid in systemically estrogenized rats certainly disrupted the neural mechanisms involved in surge, but not basal LH release. In addition, neither LHRH mRNA levels nor median eminence LHRH concentrations showed variations within the period studied when the estrogen-sensitive mechanisms involved in LH release were disrupted. Therefore, the changes in LHRH mRNA levels and LHRH concentrations in the median eminence seen in surging animals probably resulted from the same neural events which triggered LH release.
摘要 我们研究了在经雌激素处理的去卵巢大鼠中,血浆黄体生成素 (LH) 水平、中脑 LH 释放激素 (LHRH) 浓度和 LHRH mRNA 水平的时间变化,这些大鼠的内侧视前区立体定向植入了空或含有抗雌激素的微插管。两种处理都没有破坏雌激素对 LH 分泌的负反馈作用,但抗雌激素(Keoxifene)阻断了下午的 LH 激增。在表现出 LH 激增的大鼠中,中脑 LHRH 浓度在 0800、1200 和 1600 小时相似,但在 2000 小时显著升高。相比之下,在 Keoxifene 处理组中,LHRH 浓度没有发生变化。与 0800 小时相比,对照组大鼠的 LHRH mRNA 水平在 1200、1600 和 2000 小时显著升高,但在检查的时间段内,Keoxifene 处理组大鼠的 LHRH mRNA 水平没有显著变化。当我们比较随时间的治疗效果时,我们发现仅在 1600 和 2000 小时,血清 LH 水平在对照组大鼠中明显高于 Keoxifene 处理组大鼠。直到 2000 小时,两组之间的中脑 LHRH 浓度才存在差异,此时对照组动物的水平明显高于 Keoxifene 处理组动物。与对照组相比,Keoxifene 处理组大鼠的 LHRH mRNA 水平在 0800 小时显著升高,在 1600 小时显著降低。在 1200 小时或 2000 小时,两组之间的 LHRH mRNA 水平均无差异。总之,尽管尚不清楚雌激素作用于哪个神经元系统,但在全身性雌激素化的大鼠中剥夺视前区神经元的这种类固醇肯定会破坏参与激增但不参与基础 LH 释放的神经机制。此外,当涉及 LH 释放的雌激素敏感机制被破坏时,中脑 LHRH mRNA 水平和 LHRH 浓度在研究期间都没有显示出变化。因此,在表现出激增的动物中,中脑 LHRH mRNA 水平和 LHRH 浓度的变化可能是触发 LH 释放的相同神经事件的结果。