Department of Anesthesiology, University of Colorado Denver, Anschutz Medical Center, Aurora, CO 80045, USA.
Department of Neuroscience, Medical University of South Carolina, Charleston, SC 29425, USA.
Cell Rep. 2020 Feb 11;30(6):2018-2027.e3. doi: 10.1016/j.celrep.2020.01.023.
Projections from the nucleus accumbens to the ventral pallidum (VP) regulate relapse in animal models of addiction. The VP contains GABAergic (VP) and glutamatergic (VP) neurons, and a subpopulation of GABAergic neurons co-express enkephalin (VP). Rabies tracing reveals that VP and VP neurons receive preferential innervation from upstream D1- relative to D2-expressing accumbens neurons. Chemogenetic stimulation of VP neurons inhibits, whereas stimulation of VP and VP neurons potentiates cocaine seeking in mice withdrawn from intravenous cocaine self-administration. Calcium imaging reveals cell type-specific activity patterns when animals learn to suppress drug seeking during extinction training versus engaging in cue-induced cocaine seeking. During cued seeking, VP neurons increase their overall activity, and VP neurons are selectively activated around nose pokes for cocaine. In contrast, VP neurons increase their spike rate following extinction training. These data show that VP subpopulations differentially encode and regulate cocaine seeking, with VP and VP neurons facilitating and VP neurons inhibiting cocaine seeking.
伏隔核(NAc)向腹侧苍白球(VP)的投射调节成瘾动物模型中的复吸。VP 含有 GABA 能(VP)和谷氨酸能(VP)神经元,以及一小部分 GABA 能神经元共表达脑啡肽(VP)。狂犬病追踪显示,VP 和 VP 神经元优先接受来自上游表达 D1-而非 D2 的 NAc 神经元的支配。化学遗传刺激 VP 神经元抑制,而刺激 VP 和 VP 神经元增强了从静脉可卡因自我给药中戒断的小鼠对可卡因的寻求。钙成像揭示了当动物在消退训练期间抑制药物寻求与进行线索诱导的可卡因寻求时,细胞类型特异性的活动模式。在线索寻求期间,VP 神经元增加了它们的整体活动,并且 VP 神经元在可卡因的鼻探测周围被选择性地激活。相比之下,VP 神经元在消退训练后增加了它们的尖峰率。这些数据表明,VP 亚群以不同的方式对可卡因寻求进行编码和调节,VP 和 VP 神经元促进可卡因寻求,而 VP 神经元抑制可卡因寻求。