...
首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Group II metabotropic glutamate receptor-mediated regulation of dopamine release from slices of rat nucleus accumbens.
【24h】

Group II metabotropic glutamate receptor-mediated regulation of dopamine release from slices of rat nucleus accumbens.

机译:第II组代谢型谷氨酸受体介导的调节伏隔大鼠核切片中多巴胺的释放。

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

The role of metabotropic glutamate receptors (mGluRs) in the regulation of dopamine release in the rat nucleus accumbens was investigated. Fifteen millimolar of KCl stimulated the release of [(3)H]dopamine from the slices of the rat nucleus accumbens. Both an mGluR agonist 1S,3R-1-amino-cyclopentane-1,3-dicarboxylate (ACPD) and a preferential group II mGluR agonist, (2S,1'S,2'S)-2-(carboxycyclopropyl)glycine (L-CCG-1), significantly inhibited the KCl-evoked [(3)H]dopamine release in the nucleus accumbens. This inhibitory effect of L-CCG-1 on the KCl-evoked dopamine release was significantly attenuated by preferential group II mGluR antagonists such as (2S,3S,4S)-2-methyl-2-(carboxypropyl)glycine (MCCG) and (RS)-alpha-methyl-4-tetrazolylphenylglycine (MTPG); in contrast, the preferential group III mGluR agonist L-2-amino-4-phosphonobutylate (L-AP4), failed to show any effect on the KCl-evoked [(3)H]dopamine release in the nucleus accumbens. Moreover, the inhibitory effect of L-CCG-1 on the KCl-evoked [(3)H]dopamine release from the slices of the rat nucleus accumbens was preserved in the presence of tetrodotoxin. These results show that group II mGluRs may play a more significant role in regulating dopamine release than group III mGluRs, and that the group II mGluRs may negatively regulate dopamine release, presumably through those expressed at the dopaminergic nerve terminals or through those expressed at glutamatergic nerve terminals in the nucleus accumbens.
机译:研究了代谢型谷氨酸受体(mGluRs)在调节伏隔核中多巴胺释放中的作用。十五毫摩尔的氯化钾刺激[(3)H]多巴胺从大鼠伏隔核切片的释放。 mGluR激动剂1S,3R-1-氨基-环戊烷-1,3-二羧酸盐(ACPD)和II类优先mGluR激动剂(2S,1'S,2'S)-2-(羧基环丙基)甘氨酸(L-CCG-1 ),可显着抑制KCl诱发的[(3)H]多巴胺在伏隔核中的释放。 L-CCG-1对KCl诱发的多巴胺释放的这种抑制作用被优先的II型mGluR拮抗剂如(2S,3S,4S)-2-甲基-2-(羧丙基)甘氨酸(MCCG)和( RS)-α-甲基-4-四唑基苯基甘氨酸(MTPG);相比之下,优先组III mGluR激动剂L-2-氨基-4-膦酰丁酸酯(L-AP4)未能显示对伏核中KCl诱发的[(3)H]多巴胺释放的任何影响。此外,在河豚毒素存在的情况下,L-CCG-1对KCl诱发的伏安大鼠核切片中KCl诱发的[(3)H]多巴胺释放的抑制作用得以保留。这些结果表明,第二组mGluRs在调节多巴胺释放方面可能比第三组mGluRs发挥更大的作用,并且第二组mGluRs可能通过多巴胺能神经末梢表达的或谷氨酸能神经表达的负调控多巴胺的释放。伏隔核的末端。

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