Tuduri Pola, Mignon Audrey, Valjent Emmanuel, Ster Jeanne
Institut de Génomique Fonctionnelle (IGF), University of Montpellier, CNRS, INSERM, Montpellier, France.
Institut des Neurosciences de Montpellier (INM), University of Montpellier, Inserm, Montpellier, France.
Eur J Neurosci. 2025 Jul;62(1):e70176. doi: 10.1111/ejn.70176.
Spatiomolecular mapping of hippocampal dopamine D2 receptor neurons revealed that in addition to hilar mossy cells, hippocampal somatostatin interneurons and, to a lesser extent, parvalbumin interneurons expressed dopamine D2 receptor. However, the consequence of dopamine D2 receptor activation on hippocampal somatostatin interneurons and parvalbumin interneurons is unknown. By combining pharmacological approaches and patch-clamp recordings in organotypic hippocampal slices from control mice or mice lacking Drd2 selectively in somatostatin or parvalbumin interneurons, we found that dopamine D2 receptor activation increases excitability in somatostatin interneurons while it decreases it in parvalbumin interneurons in the CA1 area. These changes depend on voltage-gated K channels and rely on distinct intracellular pathways, involving the non-canonical β-arrestin-dependent pathway in somatostatin interneurons and the G protein-dependent pathway in parvalbumin interneurons. Finally, our study unveils that activation of dopamine D2 receptor in somatostatin interneurons modulates methacholine-induced rhythmic synaptic activity at 4-15 Hz.
海马多巴胺D2受体神经元的空间分子图谱显示,除了门区苔藓细胞外,海马生长抑素中间神经元以及在较小程度上的小白蛋白中间神经元也表达多巴胺D2受体。然而,多巴胺D2受体激活对海马生长抑素中间神经元和小白蛋白中间神经元的影响尚不清楚。通过结合药理学方法和对来自对照小鼠或生长抑素或小白蛋白中间神经元中选择性缺乏Drd2的小鼠的海马脑片进行膜片钳记录,我们发现多巴胺D2受体激活增加了生长抑素中间神经元的兴奋性,而降低了CA1区小白蛋白中间神经元的兴奋性。这些变化依赖于电压门控钾通道,并依赖于不同的细胞内途径,生长抑素中间神经元涉及非经典的β-抑制蛋白依赖性途径,小白蛋白中间神经元涉及G蛋白依赖性途径。最后,我们的研究揭示,生长抑素中间神经元中多巴胺D2受体的激活调节了乙酰甲胆碱诱导的4-15Hz节律性突触活动。