Department of Oral Physiology and Institute of Oral Bioscience, School of Dentistry and BK21 program, Chonbuk National University, Jeonju, South Korea.
J Neuroendocrinol. 2010 Mar;22(3):188-95. doi: 10.1111/j.1365-2826.2009.01950.x. Epub 2009 Dec 23.
There is substantial evidence for a role of the neuropeptide gonadotrophin-releasing hormone (GnRH) in the regulation of GnRH neurone secretion but how this is achieved is not understood. We examined here the effects of GnRH on the electrical excitability and intracellular calcium concentration (Ca2+) of GnRH neurones in intact adult male and female mice. Perforated-patch electrophysiological recordings from GnRH-green fluorescent protein-tagged GnRH neurones revealed that 3 nm-3 mum GnRH evoked gradual approximately 3 mV depolarisations in membrane potential from up to 50% of GnRH neurones in male and female mice. The depolarising effect of GnRH was observed on approximately 50% of GnRH neurones throughout the oestrous cycle. However, at pro-oestrus alone, GnRH was also found to transiently hyperpolarise approximately 30% of GnRH neurones. Both hyperpolarising and depolarising responses were maintained in the presence of tetrodotoxin. Calcium imaging studies undertaken in transgenic GnRH-pericam mice showed that GnRH suppressed Ca2+ in approximately 50% of GnRH neurones in dioestrous and oestrous mice. At pro-oestrus, 25% of GnRH neurones exhibited a suppressive Ca2+ response to GnRH, whereas 17% were stimulated. These results demonstrate that nm to mum concentrations of GnRH exert depolarising actions on approximately 50% of GnRH neurones in males and females throughout the oestrous cycle. This is associated with a reduction in Ca2+. At pro-oestrus, however, a further population of GnRH neurones exhibit a hyperpolarising response to GnRH. Taken together, these studies indicate that GnRH acts predominantly as a neuromodulator at the level of the GnRH cell bodies to exert a predominant excitatory influence upon GnRH neurones in intact adult male and female mice.
有大量证据表明,神经肽促性腺激素释放激素(GnRH)在 GnRH 神经元分泌的调节中起作用,但具体机制尚不清楚。我们在此研究了 GnRH 对完整成年雄性和雌性小鼠 GnRH 神经元电兴奋性和细胞内钙离子浓度(Ca2+)的影响。通过对 GnRH-绿色荧光蛋白标记的 GnRH 神经元进行穿孔贴片电生理学记录,发现 3nm-3μm GnRH 可使雄性和雌性小鼠中多达 50%的 GnRH 神经元的膜电位逐渐约 3mV 去极化。在整个发情周期中,约有 50%的 GnRH 神经元观察到 GnRH 的去极化作用。然而,只有在发情前期,GnRH 还被发现会短暂地使大约 30%的 GnRH 神经元超极化。在加入河豚毒素的情况下,去极化和超极化反应都得以维持。在 GnRH 周围 Cam 转基因小鼠中进行的钙成像研究表明,在发情间期和发情期的小鼠中,GnRH 抑制了大约 50%的 GnRH 神经元的Ca2+。在发情前期,25%的 GnRH 神经元对 GnRH 表现出抑制性Ca2+反应,而 17%的神经元则受到刺激。这些结果表明,nm 到 μm 浓度的 GnRH 在整个发情周期中对雄性和雌性的大约 50%的 GnRH 神经元产生去极化作用。这伴随着Ca2+的减少。然而,在发情前期,另一群 GnRH 神经元对 GnRH 表现出超极化反应。综上所述,这些研究表明,在完整成年雄性和雌性小鼠中,GnRH 主要作为 GnRH 细胞体的神经调质发挥作用,对 GnRH 神经元产生主要的兴奋影响。