Li S, Pelletier G
MRC Group in Molecular Endocrinology, CHUL Research Center, Sainte-Foy, Canada.
Neuroendocrinology. 1993 Jul;58(1):136-9. doi: 10.1159/000126522.
The role of GABA in the control of gonadotropin-releasing hormone (GnRH) secretion is still controversial. In order to investigate the role of the GABAergic system in the regulation of GnRH gene expression in the rat brain, we studied the effects of chronic administration (2 days) of the GABAA receptor agonist muscimol and the central-type barbiturate receptor agonist pentobarbital on GnRH mRNA levels measured by in situ hybridization. Treatment with pentobarbital produced a 24% decrease in the hybridization signal. Similarly, muscimol treatment decreased the signal by 28%. The concomitant administration of the two GABAA receptor agonists resulted in a decrease (37%) of mRNA levels which was significantly more marked than that induced by pentobarbital or muscimol alone. The present results, together with previous data, indicate that the administration of pentobarbital or muscimol can inhibit not only the release of GnRH but also the gene expression of the neuropeptide as evaluated by mRNA level measurements.
γ-氨基丁酸(GABA)在促性腺激素释放激素(GnRH)分泌调控中的作用仍存在争议。为了研究GABA能系统在大鼠大脑中GnRH基因表达调控中的作用,我们通过原位杂交检测了GABAA受体激动剂蝇蕈醇和中枢型巴比妥受体激动剂戊巴比妥慢性给药(2天)对GnRH mRNA水平的影响。戊巴比妥处理使杂交信号降低了24%。同样,蝇蕈醇处理使信号降低了28%。两种GABAA受体激动剂联合给药导致mRNA水平降低(37%),这比单独使用戊巴比妥或蝇蕈醇引起的降低更为显著。目前的结果与先前的数据表明,戊巴比妥或蝇蕈醇给药不仅可以抑制GnRH的释放,还可以抑制通过mRNA水平测量评估的神经肽的基因表达。