首页> 外文期刊>The European Journal of Neuroscience >Distinct subtypes of group I metabotropic glutamate receptors on rat spinal neurons mediate complex facilitatory and inhibitory effects.
【24h】

Distinct subtypes of group I metabotropic glutamate receptors on rat spinal neurons mediate complex facilitatory and inhibitory effects.

机译:大鼠脊髓神经元上I组代谢型谷氨酸受体的不同亚型介导复杂的促进和抑制作用。

获取原文
获取原文并翻译 | 示例
           

摘要

While group I glutamate metabotropic (mGlu) receptors show discrete neuronal distribution in the neonatal rat spinal cord, the functional role of their distinct receptor subtypes remains uncertain. Intracellular recording from lumbar motoneurons together with extracellular recording of ventral root (VR) responses was used to investigate the differential contribution by mGlu receptor subtypes to cell excitability and network activity. The group I agonist DHPG evoked motoneuron depolarization (via the AIDA or CPCCOEt-sensitive mGlu receptor subtype 1) mainly at network level and generated sustained, network-dependent oscillations (via the MPEP-sensitive mGlu receptor subtype 5). DHPG also decreased the peak amplitude of synaptic responses induced by dorsal root stimuli, an effect unrelated to depolarization and dependent on glycinergic transmission. Synaptic responses were insensitive to AIDA or MPEP. The present results can be explained by assuming excitation of discrete classes of interneurons by groupI mGlu receptor activity. Thus, the cellular distribution of those mGlu receptors at strategic circuit connections may determine the functional outcome of the network in terms of excitation or inhibition. Even if there was insufficient activation by endogenous glutamate of mGlu receptors during synaptic activity evoked by DR stimuli, it is apparent that such receptors are important pharmacological targets for powerful and rapid up- or down-regulation of spinal signal processing at network level, providing a rationale for the proposed use of mGlu receptor agonists in a variety of spinal pathological conditions.
机译:虽然I组谷氨酸代谢型(mGlu)受体在新生大鼠脊髓中显示出离散的神经元分布,但它们不同的受体亚型的功能作用仍然不确定。腰部运动神经元的胞内记录以及腹侧根(VR)反应的胞外记录用于研究mGlu受体亚型对细胞兴奋性和网络活性的不同贡献。第一组激动剂DHPG引起运动神经元去极化(通过AIDA或CPCCOEt敏感的mGlu受体亚型1),并在网络水平上引起持续的依赖网络的振荡(通过MPEP敏感的mGlu受体亚型5)。 DHPG还降低了由背根刺激引起的突触反应的峰值幅度,这种效应与去极化无关,并且依赖于甘氨酸能传递。突触反应对AIDA或MPEP不敏感。可以通过假设第i组mGlu受体活性激发离散类别的中间神经元来解释本结果。因此,这些mGlu受体在策略性电路连接处的细胞分布可以确定网络在兴奋或抑制方面的功能结果。即使在DR刺激引起的突触活动过程中,内源性谷氨酸对mGlu受体的激活作用不足,也很明显,这种受体是重要的药理靶标,可在网络水平上有效且快速地上调或下调脊髓信号的处理,从而提供在多种脊柱病理疾病中建议使用mGlu受体激动剂的基本原理。

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