Rouillon Christophe, Degoulet Mickael, Chevallier Karine, Abraini Jacques H, David Hélène N
UMR CI-NAPS 6232, Université de Caen, CNRS, CEA, Centre CYCERON, BP 5229 Boulevard Becquerel, 14074 Caen Cedex, France.
Brain Res. 2008 Mar 10;1198:44-54. doi: 10.1016/j.brainres.2008.01.025. Epub 2008 Jan 18.
Evidence for functional motor interactions between group I and group III metabotropic glutamatergic (mGlu) receptors and dopamine neurotransmission is now clearly established [David, H.N., Abraini, J.H., 2001a. The group I metabotropic glutamate receptor antagonist S-4-CPG modulates the locomotor response produced by the activation of D1-like, but not D2-like, dopamine receptors in the rat nucleus accumbens. Eur. J. Neurosci. 15, 2157-2164, David, H.N., Abraini, J.H., 2002. Group III metabotropic glutamate receptors and D1-like and D2-like dopamine receptors interact in the rat nucleus accumbens to influence locomotor activity. Eur. J. Neurosci. 15, 869-875]. Nevertheless, whether or not and how, activation of group I and blockade of group III mGlu receptors modulate the motor responses induced by the activation of dopaminergic receptors in the NAcc still remains unknown. Answering this question needs to be assessed since functional interactions between neurotransmitters in the NAcc are well known to depend upon the level of activation of glutamatergic and/or dopaminergic receptors and because the effects of glutamatergic receptor agonists and antagonists on dopaminergic receptor-mediated locomotor responses are not always reciprocal as shown in previous studies. Our results show that activation of group I mGlu receptors by DHPG in the NAcc potentiated the locomotor response induced by intra-NAcc activation of D1-like receptors and blocked those induced by D2-like presynaptic or postsynaptic receptors. Alternatively, blockade of group III mGlu receptors by MPPG in the NAcc potentiated the locomotor responses mediated by D1-like receptors and by D2-like postsynaptic receptors and inhibited that induced by D2-like presynaptic receptors. These results compiled with previous data demonstrate that group I mGlu receptors and group III mGlu receptors can modulate the locomotor responses produced by D1-like and/or D2-like receptor agonists in a complex phasic and tonic fashion.
目前,I 组和 III 组代谢型谷氨酸能(mGlu)受体与多巴胺神经传递之间功能性运动相互作用的证据已明确确立[大卫,H.N.,阿布莱尼,J.H.,2001a。I 组代谢型谷氨酸受体拮抗剂 S-4-CPG 调节大鼠伏隔核中 D1 样而非 D2 样多巴胺受体激活所产生的运动反应。《欧洲神经科学杂志》15,2157 - 2164,大卫,H.N.,阿布莱尼,J.H.,2002。III 组代谢型谷氨酸受体与 D1 样和 D2 样多巴胺受体在大鼠伏隔核中相互作用以影响运动活动。《欧洲神经科学杂志》15,869 - 875]。然而,I 组 mGlu 受体的激活以及 III 组 mGlu 受体的阻断是否以及如何调节伏隔核中多巴胺能受体激活所诱导的运动反应仍然未知。由于伏隔核中神经递质之间的功能性相互作用众所周知取决于谷氨酸能和/或多巴胺能受体的激活水平,并且正如先前研究所表明的,谷氨酸能受体激动剂和拮抗剂对多巴胺能受体介导的运动反应的影响并不总是相互的,因此需要评估这个问题。我们的结果表明,在伏隔核中通过 DHPG 激活 I 组 mGlu 受体会增强伏隔核内 D1 样受体激活所诱导的运动反应,并阻断由 D2 样突触前或突触后受体所诱导的反应。另外,在伏隔核中通过 MPPG 阻断 III 组 mGlu 受体会增强由 D1 样受体和 D2 样突触后受体介导的运动反应,并抑制由 D2 样突触前受体所诱导的反应。这些结果与先前的数据汇总表明,I 组 mGlu 受体和 III 组 mGlu 受体可以以复杂的相位性和紧张性方式调节 D1 样和/或 D2 样受体激动剂所产生的运动反应。