Chu Zhiguo, Moenter Suzanne M
Department of Internal Medicine, University of Virginia, Charlottesville, Virginia 22908, USA.
J Neurosci. 2005 Jun 15;25(24):5740-9. doi: 10.1523/JNEUROSCI.0913-05.2005.
Gonadotropin-releasing hormone (GnRH) neurons are the primary central regulators of fertility, receiving input from GABAergic afferents via GABA(A) receptors. We tested whether metabotropic glutamate receptors (mGluRs) regulate GABA transmission to GnRH neurons and GnRH neuronal firing pattern. Whole-cell recordings were performed under conditions isolating ionotropic GABA postsynaptic currents (PSCs) in brain slices. The broad-spectrum mGluR agonist 1-aminocyclopentane-1,3-dicarboxylic acid (ACPD) decreased the frequency of GABA(A)-mediated spontaneous PSCs in a reversible manner. Amplitude and kinetics were not altered, suggesting that afferent GABA neurons are the primary targets. TTX eliminated the effects of ACPD in most tested neurons. Group II [2-(2,3-dicarboxycyclopropyl) glycine] and III (L-AP-4) mGluR agonists mediated this response; a group I agonist (3,5-dihydroxyphenylglycine) was not effective. The broad-spectrum antagonist alpha-methyl-4-carboxyphenylglycine (MCPG) and/or (RS)-alpha-cyclopropyl-4-phosphonophenylglycine (CPPG) (group III antagonist) enhanced spontaneous PSC frequency, particularly when initial frequency was low, suggesting that endogenous activation of mGluRs regulates GABA transmission to GnRH neurons. Extracellular recordings were used to evaluate GnRH neuron firing rate within the network. ACPD reduced firing rate, and MCPG plus CPPG had an opposite effect, indicating that mGluRs help control excitability of the GnRH network. GnRH neurons express vesicular glutamate transporters, suggesting they may corelease this transmitter. Simulation of firing activity in a GnRH neuron decreased PSC frequency in that cell, an effect blocked by antagonism of mGluRs but not GnRH receptors. These results demonstrate an inhibition of GABAergic inputs to GnRH neurons by mGluRs via a presynaptic mechanism. Through this mechanism, local glutamate milieu, possibly contributed by GnRH neurons themselves, plays an important role in modulating GnRH release and the central regulation of fertility.
促性腺激素释放激素(GnRH)神经元是生育能力的主要中枢调节者,通过GABA(A)受体接收来自GABA能传入神经的输入。我们测试了代谢型谷氨酸受体(mGluRs)是否调节GABA向GnRH神经元的传递以及GnRH神经元的放电模式。在分离脑片中离子型GABA突触后电流(PSCs)的条件下进行全细胞记录。广谱mGluR激动剂1-氨基环戊烷-1,3-二羧酸(ACPD)以可逆方式降低了GABA(A)介导的自发性PSCs的频率。幅度和动力学未改变,表明传入GABA神经元是主要靶点。河豚毒素在大多数测试神经元中消除了ACPD的作用。II组[2-(2,3-二羧基环丙基)甘氨酸]和III组(L-AP-4)mGluR激动剂介导了这种反应;I组激动剂(3,5-二羟基苯甘氨酸)无效。广谱拮抗剂α-甲基-4-羧基苯甘氨酸(MCPG)和/或(RS)-α-环丙基-4-膦酰基苯甘氨酸(CPPG)(III组拮抗剂)增加了自发性PSC频率,特别是当初始频率较低时,表明mGluRs的内源性激活调节GABA向GnRH神经元的传递。细胞外记录用于评估网络内GnRH神经元的放电率。ACPD降低了放电率,而MCPG加CPPG则有相反的作用,表明mGluRs有助于控制GnRH网络的兴奋性。GnRH神经元表达囊泡谷氨酸转运体,表明它们可能共同释放这种递质。模拟GnRH神经元的放电活动降低了该细胞中的PSC频率,这种效应被mGluRs拮抗剂而非GnRH受体拮抗剂阻断。这些结果表明mGluRs通过突触前机制抑制GABA能输入到GnRH神经元。通过这种机制,可能由GnRH神经元自身贡献的局部谷氨酸环境在调节GnRH释放和生育能力的中枢调节中起重要作用。