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Purinergic P2X Receptors Presynaptically Increase Glutamatergic Synaptic Transmission in Dorsolateral Periaqueductal Gray

机译:Purinergic P2X受体突触增加臀外侧Pyorqueductal灰色的谷氨酸能突触传递。

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摘要

Purinergic P2X receptors have been reported to present in regions of the midbrain periaqueductal gray (PAG). The purpose of this study was to determine the role of presynaptic P2X receptors in modulating excitatory and inhibitory synaptic inputs to the dorsolateral PAG (dl-PAG), which has abundant neuronal connections. First, whole cell voltage-clamp recording was performed to obtain excitatory and inhibitory postsynaptic currents (EPSCs and IPSCs) of the dl-PAG neurons. Our data show that α, β-methylene ATP (a P2X receptors agonist), in the concentration of 50 µM, significantly increased the frequency of miniature EPSCs without altering the amplitude of miniature EPSCs in eight tested neurons. The effects were attenuated by PPADS, an antagonist to P2X receptors. Furthermore, α, β-methylene ATP increased the amplitude of evoked EPSCs, and decreased the paired-pulse ratio of eEPSCs in ten neurons. In contrast, activation of P2X had no distinct effect on IPSCs. In addition, immunofluoresent methods demonstrate that P2X labeling was co-localized with a presynaptic marker, synaptophysin, in the dl-PAG. The results of the current study provide the first evidence indicating that P2X receptors facilitate glutamatergic synaptic transmission in the dl-PAG via presynaptic mechanisms.
机译:嘌呤能P2X受体据报道存在于中脑导水管灰色(PAG)区域。这项研究的目的是确定突触前P2X受体在调节具有丰富神经元联系的背外侧PAG(dl-PAG)的兴奋性和抑制性突触输入中的作用。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)。我们的数据表明,浓度为50 µM的α,β-亚甲基ATP(一种P2X受体激动剂)可显着增加微型EPSC的频率,而不会改变八个测试神经元中微型EPSC的幅度。 P2X受体的拮抗剂PPADS减弱了这种作用。此外,α,β-亚甲基ATP增加了10个神经元中诱发的EPSC的幅度,并降低了eEPSC的成对脉冲比。相反,P2X的激活对IPSC没有明显影响。此外,免疫荧光方法证明P2X标记与dl-PAG中的突触前标记突触素共定位。当前研究的结果提供了第一个证据,表明P2X受体通过突触前机制促进dl-PAG中的谷氨酸能突触传递。

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  • 作者

    Jihong Xing; Jian Lu; Jianhua Li;

  • 作者单位
  • 年(卷),期 -1(1208),-1
  • 年度 -1
  • 页码 46–55
  • 总页数 16
  • 原文格式 PDF
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