...
首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Activation of metabotropic glutamate 5 (mGlu5) receptors induces spontaneous excitatory synaptic currents in layer V pyramidal cells of the rat prefrontal cortex.
【24h】

Activation of metabotropic glutamate 5 (mGlu5) receptors induces spontaneous excitatory synaptic currents in layer V pyramidal cells of the rat prefrontal cortex.

机译:代谢型谷氨酸5(mGlu5)受体的激活在大鼠前额叶皮层的V层锥体细胞中诱导自发性兴奋性突触电流。

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

Serotonin and norepinephrine, in addition to direct postsynaptic excitatory effects, also enhances glutamate release onto layer V pyramidal cells of the prefrontal cortexeocortex via G(q/11)-coupled 5-hydroxytryptamine(2A) (5-HT(2A)) and alpha(1)-adrenergic receptors, respectively. Therefore, the present study was designed to test whether a metabotropic glutamate (mGlu) receptor subtype also coupled to G(q/11)-proteins, the mGlu5 receptor, also induces EPSCs when recording from layer V cortical pyramidal cells of the rat medial prefrontal cortex (mPFC). The mGlu1/5 receptor agonist (S)-3,5-dihydroxyphenylglycine (DHPG) induces EPSCs at a similar frequency as a near-maximally effective 5-HT concentration. The mGlu5 receptor negative allosteric modulator 2-methyl-6-(phenylethynyl)pyridine (MPEP, 300 nM) potently blocked DHPG-induced EPSCs. Previous work has suggested that activation of 5-HT(2A) and OX2 receptors induces glutamate release, while mGlu2, mGlu4, and mGlu8 receptor activation suppress transmitter release from thalamocortical terminals. Taken together with past results, these findings suggest that mGlu2, mGlu4, mGlu5 and mGlu8 may all act to modulate glutamate release from afferents impinging on layer V pyramidal cells of the mPFC. These findings further suggest that monoamines, neuropeptides and glutamate itself all enhance the excitability of prefrontal cortical output cells indirectly via modulation of glutamate release.
机译:5-羟色胺和去甲肾上腺素除了直接的突触后兴奋作用外,还通过G(q / 11)偶联的5-羟基色胺(2A)(5-HT(2A))增强谷氨酸释放到前额叶皮层/新皮层的V层锥体细胞中。和α(1)-肾上腺素受体。因此,本研究旨在测试是否从大鼠内侧前额叶的第V层皮质锥体细胞记录时,代谢型谷氨酸(mGlu)受体亚型也与G(q / 11)蛋白mGlu5受体偶联也诱导EPSC。皮质(mPFC)。 mGlu1 / 5受体激动剂(S)-3,5-二羟基苯基甘氨酸(DHPG)诱导EPSC的频率与接近最大有效5-HT浓度的频率相似。 mGlu5受体阴性的变构调节剂2-甲基-6-(苯基乙炔基)吡啶(MPEP,300 nM)有效地阻断了DHPG诱导的EPSC。以前的工作表明,激活5-HT(2A)和OX2受体会诱导谷氨酸释放,而mGlu2,mGlu4和mGlu8受体激活会抑制变送器从丘脑皮层末端释放。结合过去的结果,这些发现表明,mGlu2,mGlu4,mGlu5和mGlu8可能都起着调节从撞击mPFC的V层锥体细胞的传入物质释放谷氨酸的作用。这些发现进一步表明,单胺,神经肽和谷氨酸本身都可以通过调节谷氨酸的释放而间接增强前额叶皮层输出细胞的兴奋性。

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