Owesson-White Catarina A, Ariansen Jennifer, Stuber Garret D, Cleaveland Nathan A, Cheer Joseph F, Wightman R Mark, Carelli Regina M
Department of Psychology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Eur J Neurosci. 2009 Sep;30(6):1117-27. doi: 10.1111/j.1460-9568.2009.06916.x. Epub 2009 Sep 4.
Mesolimbic dopamine neurons projecting from the ventral tegmental area to the nucleus accumbens (NAc) are part of a complex circuit mediating cocaine-directed behaviors. However, the precise role of rapid (subsecond) dopamine release within the primary subregions of the NAc (the core and shell) and its relationship to NAc cell firing during this behavior remain unknown. Here, using fast-scan cyclic voltammetry in rats we report rapid dopamine signaling in both the core and shell; however, significant differences were observed in the timing of dopamine release events within seconds of the cocaine-reinforced response during self-administration sessions. Importantly, simultaneous voltammetric and electrophysiological recordings from the same electrode reveal that, at certain sites within both subregions, neurons exhibiting patterned activation were observed at locations where rapid dopamine release was present; the greater the strength of the neural signal the larger the dopamine release event. In addition, it was at those locations that electrically-evoked stimulated release was greatest. No changes in dopamine were observed where nonphasic neurons were recorded. Thus, although differences are evident in dopamine release dynamics relative to cocaine-reinforced responding within the core and shell, dopamine release is heterogeneous within each structure and varies as a function of precise neuronal targets during cocaine-seeking behavior.
从中脑腹侧被盖区投射到伏隔核(NAc)的中脑边缘多巴胺神经元是介导可卡因相关行为的复杂神经回路的一部分。然而,NAc主要亚区(核心区和壳区)内快速(亚秒级)多巴胺释放的确切作用及其在此行为过程中与NAc细胞放电的关系仍不清楚。在此,我们利用对大鼠进行的快速扫描循环伏安法,报告了核心区和壳区内的快速多巴胺信号;然而,在自我给药过程中,可卡因强化反应数秒内多巴胺释放事件的时间上观察到了显著差异。重要的是,从同一电极同时进行的伏安法和电生理记录显示,在两个亚区的某些位点,在存在快速多巴胺释放的位置观察到了表现出模式化激活的神经元;神经信号强度越大,多巴胺释放事件越大。此外,正是在这些位置,电诱发的刺激释放最大。在记录到非相位神经元的地方未观察到多巴胺变化。因此,尽管相对于核心区和壳区内可卡因强化反应,多巴胺释放动态存在明显差异,但在每种结构内多巴胺释放是异质性的,并且在觅药行为期间随精确的神经元靶点而变化。