Mamad Omar, Delaville Claire, Benjelloun Wail, Benazzouz Abdelhamid
Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, F-33000, Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000, Bordeaux, France; Université Mohamed V-Agdal, Faculté des Sciences, Equipe Rythmes Biologiques, Neurosciences et Environnement, 10000, Rabat, Morocco.
Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, F-33000, Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000, Bordeaux, France.
PLoS One. 2015 Mar 5;10(3):e0119152. doi: 10.1371/journal.pone.0119152. eCollection 2015.
The globus pallidus (GP) receives dopaminergic afferents from the pars compacta of substantia nigra and several studies suggested that dopamine exerts its action in the GP through presynaptic D2 receptors (D2Rs). However, the impact of dopamine in GP on the pallido-subthalamic and pallido-nigral neurotransmission is not known. Here, we investigated the role of dopamine, through activation of D2Rs, in the modulation of GP neuronal activity and its impact on the electrical activity of subthalamic nucleus (STN) and substantia nigra reticulata (SNr) neurons. Extracellular recordings combined with local intracerebral microinjection of drugs were done in male Sprague-Dawley rats under urethane anesthesia. We showed that dopamine, when injected locally, increased the firing rate of the majority of neurons in the GP. This increase of the firing rate was mimicked by quinpirole, a D2R agonist, and prevented by sulpiride, a D2R antagonist. In parallel, the injection of dopamine, as well as quinpirole, in the GP reduced the firing rate of majority of STN and SNr neurons. However, neither dopamine nor quinpirole changed the tonic discharge pattern of GP, STN and SNr neurons. Our results are the first to demonstrate that dopamine through activation of D2Rs located in the GP plays an important role in the modulation of GP-STN and GP-SNr neurotransmission and consequently controls STN and SNr neuronal firing. Moreover, we provide evidence that dopamine modulate the firing rate but not the pattern of GP neurons, which in turn control the firing rate, but not the pattern of STN and SNr neurons.
苍白球(GP)接受来自黑质致密部的多巴胺能传入纤维,多项研究表明多巴胺通过突触前D2受体(D2Rs)在苍白球发挥作用。然而,多巴胺在苍白球中对苍白球 - 丘脑底核和苍白球 - 黑质神经传递的影响尚不清楚。在此,我们通过激活D2Rs研究了多巴胺在调节苍白球神经元活动及其对丘脑底核(STN)和黑质网状部(SNr)神经元电活动影响中的作用。在乌拉坦麻醉下,对雄性Sprague - Dawley大鼠进行细胞外记录并结合药物局部脑内微注射。我们发现,局部注射多巴胺可增加苍白球中大多数神经元的放电频率。D2R激动剂喹吡罗可模拟这种放电频率的增加,而D2R拮抗剂舒必利可阻止这种增加。同时,在苍白球中注射多巴胺以及喹吡罗可降低大多数STN和SNr神经元的放电频率。然而,多巴胺和喹吡罗均未改变苍白球、STN和SNr神经元的紧张性放电模式。我们的结果首次证明,多巴胺通过激活位于苍白球的D2Rs在调节苍白球 - STN和苍白球 - SNr神经传递中起重要作用,从而控制STN和SNr神经元的放电。此外,我们提供证据表明多巴胺调节苍白球神经元的放电频率而非放电模式,而苍白球神经元又控制STN和SNr神经元的放电频率而非放电模式。