Rothfeld J, Hejtmancik J F, Conn P M, Pfaff D W
Rockefeller University, New York, NY 10021.
Brain Res Mol Brain Res. 1989 Nov;6(2-3):121-5. doi: 10.1016/0169-328x(89)90045-4.
Elucidation of mechanisms governing the synthesis and release of the decapeptide luteinizing hormone-releasing hormone (LHRH) in the female are central for understanding how the brain influences the ovulatory surge of luteinizing hormone and facilitates female rat mating behavior. Previous immunocytochemical results suggested that estrogen treatment might increase LHRH forebrain content, but measures of peptide content often are confounded by alterations in synthesis versus peptide processing versus release. Therefore, we have used in situ hybridization with an oligomer for the LHRH coding region to detect LHRH gene expressing cells and to study LHRH message levels in estrogen treated compared to control ovariectomized rats. Neurons expressing the gene for LHRH are in the medial preoptic area and amongst the fibers of the diagonal bands of Broca. When the numbers of neurons with detectable LHRH message levels were multiplied by the average numbers of grains per cell, to achieve a metric proportional to LHRH message content, we saw a significant stimulatory effect of seven days of estrogen treatment.
阐明雌性体内十肽促黄体激素释放激素(LHRH)的合成和释放机制,对于理解大脑如何影响促黄体激素的排卵高峰以及促进雌性大鼠的交配行为至关重要。先前的免疫细胞化学结果表明,雌激素处理可能会增加LHRH在前脑的含量,但肽含量的测量常常因合成、肽加工和释放的改变而混淆。因此,我们使用针对LHRH编码区的寡聚物进行原位杂交,以检测表达LHRH基因的细胞,并研究与对照去卵巢大鼠相比,雌激素处理后的LHRH信使水平。表达LHRH基因的神经元位于内侧视前区和布洛卡斜带的纤维之间。当将具有可检测到的LHRH信使水平的神经元数量乘以每个细胞的平均颗粒数,以获得与LHRH信使含量成比例的指标时,我们发现雌激素处理七天具有显著的刺激作用。