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Prostaglandin E2 (PGE2) Inhibits Glutamatergic Synaptic Transmission in Dorsolateral Periaqueductal Gray (dl-PAG)

机译:前列腺素E2(PGE2)抑制背外侧胸膜前导灰色(dl-PAG)的谷氨酸能突触传递。

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摘要

The purpose of this study was to determine the role of prostaglandin E2 (PGE2) in modulating neuronal activity of the dorsolateral periaqueductal gray (dl-PAG) through excitatory and inhibitory synaptic inputs. First, whole cell voltage-clamp recording was performed to obtain excitatory and inhibitory postsynaptic currents (EPSCs and IPSCs) of the dl-PAG neurons. Our results show that PGE2 significantly decreased the frequency of miniature EPSCs and amplitude of evoked EPSCs. The effects were mimicked by sulprostone, an agonist to PGE2 EP3 receptors. In contrast, PGE2 had no distinct effect on IPSCs. In addition, spontaneous action potential of the dl-PAG neurons was recorded using whole cell current-clamp methods. PGE2 significantly attenuated the discharge rate of the dl-PAG neurons. The decreased firing activity was abolished in the presence of glutamate NMDA and non-NMDA receptors antagonists. The results from the current study provide the first evidence indicating that PGE2 inhibits the neuronal activity of the dl-PAG via selective attenuation of glutamatergic synaptic inputs, likely due to activation of presynaptic EP3 receptors.
机译:这项研究的目的是确定前列腺素E2(PGE2)在通过兴奋性和抑制性突触输入来调节背外侧导水管周围灰色(dl-PAG)的神经元活性中的作用。首先,进行全细胞电压钳记录,以获得dl-PAG神经元的兴奋性和抑制性突触后电流(EPSC和IPSC)。我们的结果表明,PGE2显着降低了微型EPSC的频率和诱发的EPSC的幅度。这种作用被舒美通酮(PGE2 EP3受体的激动剂)模仿。相反,PGE2对IPSC没有明显影响。此外,使用全细胞电流钳方法记录了dl-PAG神经元的自发动作电位。 PGE 2显着减弱了dl-PAG神经元的放电速率。在谷氨酸NMDA和非NMDA受体拮抗剂的存在下消除了降低的射击活性。当前研究的结果提供了第一个证据,表明PGE2通过选择性减弱谷氨酸能突触输入来抑制dl-PAG的神经元活性,这可能是由于突触前EP3受体的激活所致。

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