Department of Pharmacology, Shanghai Institute of Materia Medica, Shanghai, 201203, China.
Cambrian Discovery Inc, Dover, MA, 02030, USA.
Sci Rep. 2018 Feb 19;8(1):3274. doi: 10.1038/s41598-018-21592-7.
The initiation of psychostimulant sensitization depends on the mesocorticolimbic dopamine (DA) system. Although many cellular adaptations has been reported to be associated with this addictive behavior, the overall influence of these adaptations on the network regulation of DA neurons has not been established. Here, we profile a network-driven slow oscillation (SO) in the firing activity of ventral tegmental area (VTA) putative DA and non-DA neurons and their correlation with locomotor sensitization induced by repeated administration of cocaine. One day after the last cocaine injection, the power of SO (Pso) significantly increased both in DA and non-DA neurons. Interestingly, the Pso in DA neurons was positively correlated, while Pso in non-DA neurons was negatively correlated with the level of locomotor sensitization. On the other hand, the firing rates of DA and non-DA neurons were both elevated, but none exhibited any correlation with the level of sensitization. Fourteen days after the last injection, the Pso of DA neurons dissipated but still positively correlated with the level of sensitization. In contrast, the Pso in non-DA neurons lost correlation with locomotor sensitization. These results suggest that cocaine-induced locomotor sensitization is associated with long-term network adaptation in DA system and that DA and non-DA neurons may corporately facilitate/hamper the initiation of locomotor sensitization.
药物敏化的启动依赖于中脑边缘多巴胺(DA)系统。虽然已经报道了许多与这种成瘾行为相关的细胞适应,但这些适应对 DA 神经元网络调节的总体影响尚未确定。在这里,我们对腹侧被盖区(VTA)中 DA 和非 DA 神经元的网络驱动慢波(SO)的活动进行了描绘,并分析了它们与重复给予可卡因诱导的运动敏化之间的相关性。在最后一次可卡因注射后的一天,DA 和非 DA 神经元的 SO 功率(Pso)均显著增加。有趣的是,DA 神经元中的 Pso 呈正相关,而非 DA 神经元中的 Pso 则与运动敏化水平呈负相关。另一方面,DA 和非 DA 神经元的放电率均升高,但均与敏化水平无关。最后一次注射 14 天后,DA 神经元的 Pso 消失,但仍与敏化水平呈正相关。相比之下,非 DA 神经元的 Pso 与运动敏化失去相关性。这些结果表明,可卡因诱导的运动敏化与 DA 系统的长期网络适应有关,DA 和非 DA 神经元可能共同促进/阻碍运动敏化的启动。