...
首页> 外文期刊>Neuropharmacology >5-HT1A receptors direct the orientation of plasticity in layer 5 pyramidal neurons of the mouse prefrontal cortex
【24h】

5-HT1A receptors direct the orientation of plasticity in layer 5 pyramidal neurons of the mouse prefrontal cortex

机译:5-HT1A受体指导小鼠前额叶皮质第5层锥体神经元的可塑性方向

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Several psychiatric disorders involving the prefrontal cortex (PFC) are associated with a dysfunction of 5-HT1A receptors (5-HT 1AR). These receptors, located on interneurons and pyramidal neurons, may influence neuronal excitability through a regulation of the balance between excitation (E) and inhibition (I). Patch-clamp recordings in mouse cortical slices were performed to determine the modulatory role of 5-HT1AR on the excitability and the synaptic plasticity of layer 5 pyramidal neurons (L5PyNs) of the PFC. This was done by a comparison of postsynaptic currents evoked by electrical stimulation in layer 2/3 of 5-HT1AR-KO and wild-type (WT) mice. We observed that the E-I balance was significantly changed from 20% E-80% I in WT mice to 23% E-77% I in 5-HT1AR-KO mice, demonstrating that 5-HT1ARs contribute to the control of the balance between excitation and inhibition. Furthermore, we show that interfering with 5-HT1AR reduced the magnitude of the long term potentiation of excitation (eLTP) (induced by high frequency stimulation). In addition, we show that 5-HT1ARs determine the orientation of the synaptic plasticity towards LTP or LTD or no plasticity through the modulation of NMDAR-mediated currents. Our data point out to a unique role of 5-HT 1A postsynaptic receptors in PFC to adapt the functional plasticity of L5PyNs towards LTP, LTD or no plasticity. This brings a new way to intervene on neuronal networks of the PFC in anxiety disorders and schizophrenia.
机译:几种涉及前额叶皮层(PFC)的精神疾病与5-HT1A受体(5-HT 1AR)的功能障碍有关。这些位于中间神经元和锥体神经元上的受体可能通过调节兴奋(E)和抑制(I)之间的平衡来影响神经元兴奋性。在小鼠皮质切片中进行膜片钳记录,以确定5-HT1AR对PFC的第5层锥体神经元(L5PyNs)的兴奋性和突触可塑性的调节作用。通过比较5-HT1AR-KO和野生型(WT)小鼠2/3层的电刺激诱发的突触后电流来完成此操作。我们观察到EI平衡从WT小鼠中的20%E-80%I变为5-HT1AR-KO小鼠中的23%E-77%I,表明5-HT1ARs有助于控制激发之间的平衡和抑制。此外,我们表明干扰5-HT1AR降低了长期激发的增强电位(eLTP)(由高频刺激引起)。此外,我们表明,5-HT1ARs通过调节NMDAR介导的电流来确定突触可塑性朝向LTP或LTD的方向或没有可塑性。我们的数据指出了5-HT 1A突触后受体在PFC中的独特作用,以使L5PyNs的功能可塑性适应LTP,LTD或无可塑性。这为干预焦虑症和精神分裂症的PFC神经网络带来了新的途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号