Park O K, Gugneja S, Mayo K E
Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, Illinois 60208.
Endocrinology. 1990 Jul;127(1):365-72. doi: 10.1210/endo-127-1-365.
Although hypothalamic GnRH release is known to be modulated by neural and hormonal factors, the relationship between altered GnRH secretion and GnRH synthesis remains unclear. In an attempt to address this question, we examined GnRH gene expression in the rat hypothalamus using in situ hybridization histochemistry. An 25S-labeled antisense RNA probe was used to identify neurons expressing GnRH mRNA in an area that included the diagonal band of Broca, the organum vasculosum of the lamina terminalis, and the preoptic area. The number of GnRH mRNA-expressing cells was determined at various times during the rat estrous cycle. During proestrus, the number of GnRH mRNA-expressing cells decreased somewhat at 1400-1600 h, increased significantly at 1800 h (the time of the LH surge), then gradually returned to basal levels at 2200 h. Expression did not change substantially at other times during the estrous cycle. To understand this close temporal relationship between the LH surge and increased GnRH mRNA levels, we examined GnRH gene expression in proestrous animals in which the LH surge was blocked with pentobarbital. Pentobarbital treatment blocked the increase in the number of GnRH mRNA-expressing cells normally observed at 1800 h in saline-treated controls, suggesting that the increase in GnRH gene expression is closely coupled to secretion of GnRH from the hypothalamus. Finally, we addressed the question of whether ovarian steroids have direct effects on GnRH gene expression by examining GnRH mRNA levels in ovariectomized steroid-treated rats at a time before (1100 h) and a time after (1800 h) hypothalamic GnRH hypersecretion. At 1100 h, no significant changes were observed, but at 1800 h, estrogen-treated rats showed a significant increase in both the number of GnRH mRNA-expressing cells and serum LH levels. This suggests that estrogen influences GnRH gene expression indirectly, perhaps by altering hypothalamic GnRH release. Our results in each of these models suggest that GnRH mRNA levels increase in response to GnRH hypersecretion at the time of the LH surge.
虽然已知下丘脑促性腺激素释放激素(GnRH)的释放受神经和激素因素调节,但GnRH分泌改变与GnRH合成之间的关系仍不清楚。为了解决这个问题,我们使用原位杂交组织化学技术研究了大鼠下丘脑GnRH基因的表达。用一个25S标记的反义RNA探针来鉴定在包括布罗卡斜带、终板血管器和视前区在内的区域中表达GnRH mRNA的神经元。在大鼠发情周期的不同时间点测定表达GnRH mRNA的细胞数量。在发情前期,表达GnRH mRNA的细胞数量在1400 - 1600时略有减少,在1800时(促黄体生成素峰出现的时间)显著增加,然后在2200时逐渐恢复到基础水平。在发情周期的其他时间,表达没有实质性变化。为了理解促黄体生成素峰与GnRH mRNA水平升高之间这种紧密的时间关系,我们研究了用戊巴比妥阻断促黄体生成素峰的发情前期动物的GnRH基因表达。戊巴比妥处理阻断了在生理盐水处理的对照动物中通常在1800时观察到的表达GnRH mRNA的细胞数量增加,这表明GnRH基因表达的增加与下丘脑GnRH的分泌密切相关。最后,我们通过检测去卵巢并用类固醇处理的大鼠在促性腺激素释放激素(GnRH)分泌过多之前(1100时)和之后(1800时)的GnRH mRNA水平,来探讨卵巢类固醇是否对GnRH基因表达有直接影响。在1100时,未观察到显著变化,但在1800时,雌激素处理的大鼠表达GnRH mRNA的细胞数量和血清促黄体生成素水平均显著增加。这表明雌激素可能通过改变下丘脑GnRH的释放间接影响GnRH基因表达。我们在这些模型中的每一个结果都表明,在促黄体生成素峰出现时,GnRH mRNA水平会因GnRH分泌过多而升高。