Rossmanith W G, Marks D L, Steiner R A, Clifton D K
Department of Obstetrics-Gynecology, University of Washington, Seattle 98195, USA.
J Neuroendocrinol. 1996 Mar;8(3):179-84. doi: 10.1046/j.1365-2826.1996.04462.x.
Galanin mRNA levels in GnRH neurons increase in association with a steroid-induced LH surge in female rats. Both the steroid-induced LH surge and the concomitant increase of galanin mRNA in GnRH neurons are blocked by non-specific inhibition of central nervous system activity imposed by pentobarbital and specific central alpha-adrenergic receptor blockade. Based on these observations, we hypothesized that galanin gene expression in GnRH neurons is induced whenever GnRH neurons become activated to generate an LH surge. If this were the case, then any neurotransmitter receptor blocking agent that inhibits the LH surge by central mechanisms would likewise block the associated increase in galanin mRNA in GnRH neurons. We tested this hypothesis by examining the effects of an N-methyl-D-aspartate (NMDA) receptor antagonist on the steroid-induced LH surge and on levels of galanin mRNA in GnRH neurons. Three groups of ovariectomized rats were used: Group 1 -treated with estradiol and progesterone (E/P) and sacrificed at the peak of the LH surge; Group 2-treated the same as Group 1 except that dizocilpine (MK801, an NMDA receptor antagonist) was used to block the LH surge; and Group 3-treated the same as Group 1 except they received vehicle instead of E/P. Double-and single-label in situ hybridization followed by computerized image analysis were used to measure levels of galanin mRNA and GnRH mRNA in GnRH neurons [as grains/cell (g/c)]. E/P treatment induced a 3-fold increase in LH levels and a 5-fold increase in the galanin mRNA signal content of GnRH neurons. Treatment with MK801 completely prevented the LH surge in all animals and also blocked the steroid-induced increase in galanin mRNA in GnRH neurons. As assessed by 2 independent GnRH single-labeled assays, neither GnRH message content nor the number of identifiable GnRH neurons differed among the experimental groups. We conclude that the increase in galanin mRNA levels in GnRH neurons is tightly coupled to the occurrence of a steroid-evoked LH surge, and we infer that induction of galanin gene expression in GnRH neurons is induced as a consequence of synaptic activation of GnRH neurons.
在雌性大鼠中,促性腺激素释放激素(GnRH)神经元中的甘丙肽mRNA水平会随着类固醇诱导的促黄体生成素(LH)峰而增加。戊巴比妥对中枢神经系统活动的非特异性抑制以及特异性中枢α-肾上腺素能受体阻断,均可阻断类固醇诱导的LH峰以及GnRH神经元中甘丙肽mRNA的相应增加。基于这些观察结果,我们推测,只要GnRH神经元被激活以产生LH峰,GnRH神经元中的甘丙肽基因表达就会被诱导。如果是这样的话,那么任何通过中枢机制抑制LH峰的神经递质受体阻断剂,同样也会阻断GnRH神经元中甘丙肽mRNA的相关增加。我们通过研究N-甲基-D-天冬氨酸(NMDA)受体拮抗剂对类固醇诱导的LH峰以及GnRH神经元中甘丙肽mRNA水平的影响,来验证这一假设。使用了三组去卵巢大鼠:第1组用雌二醇和孕酮(E/P)处理,并在LH峰的峰值时处死;第2组的处理与第1组相同,只是使用地佐环平(MK801,一种NMDA受体拮抗剂)来阻断LH峰;第3组的处理与第1组相同,只是它们接受的是溶剂而非E/P。采用双重和单标记原位杂交,随后进行计算机图像分析,以测量GnRH神经元中甘丙肽mRNA和GnRH mRNA的水平[以颗粒/细胞(g/c)表示]。E/P处理使LH水平增加了3倍,GnRH神经元中甘丙肽mRNA信号含量增加了5倍。用MK801处理完全阻止了所有动物的LH峰,并且也阻断了类固醇诱导的GnRH神经元中甘丙肽mRNA的增加。通过2项独立GnRH单标记检测评估,各实验组之间的GnRH信息含量和可识别的GnRH神经元数量均无差异。我们得出结论,GnRH神经元中甘丙肽mRNA水平的增加与类固醇诱发的LH峰的出现紧密相关,并且我们推断,GnRH神经元中甘丙肽基因表达的诱导是GnRH神经元突触激活的结果。