Doherty James M, Schier Christina J, Vena Ashley A, Dilly Geoffrey A, Gonzales Rueben A
Division of Pharmacology, College of Pharmacy, The University of Texas at Austin, Austin, Texas.
Alcohol Clin Exp Res. 2016 Aug;40(8):1662-70. doi: 10.1111/acer.13141. Epub 2016 Jul 20.
Medial prefrontal cortex (mPFC) dysfunction is present in heavy alcohol consumers. Dopamine signaling in mPFC is associated with executive functioning and affects drinking behavior; however, direct measurement of extracellular mPFC dopamine during appetitive and consummatory ethanol (EtOH) self-administration behavior has not been reported.
We used in vivo microdialysis in freely behaving, adult, male, Long Evans rats to determine extracellular dopamine concentration in the mPFC during operant self-administration of an EtOH-plus-sucrose or sucrose solution. The model separated appetitive/seeking from consummatory phases of the operant session. Dopamine was also monitored in an untrained handling control group, and dialysate EtOH was measured in the EtOH-drinking group.
Home cage baseline dopamine was lower in rats that experienced a week of drinking sweetened EtOH compared with sucrose-drinking and handling controls. Transfer into the operant chamber and the initiation of consumption stimulated a relatively higher change in dopamine over baseline in the sweetened EtOH group compared with sucrose and handling controls. However, all groups show a dopamine response during transfer into the operant chamber, and the sucrose group had a relatively higher change in dopamine over baseline during initiation of consumption compared with handling controls. The time courses of dopamine and EtOH in the mPFC differ in the EtOH-consuming rats.
Differences in extracellular mPFC dopamine between EtOH drinkers compared with control groups suggest that mPFC dopamine is involved in the mechanism of operant self-administration of sweetened EtOH and sucrose. Furthermore, the increase in dopamine during consumption is consistent with a role of mPFC dopamine in reward prediction.
重度饮酒者存在内侧前额叶皮质(mPFC)功能障碍。mPFC中的多巴胺信号与执行功能相关,并影响饮酒行为;然而,在有食欲和完成乙醇(EtOH)自我给药行为期间,尚未有对细胞外mPFC多巴胺的直接测量报道。
我们对自由活动的成年雄性Long Evans大鼠进行了体内微透析,以确定在操作性自我给药EtOH加蔗糖或蔗糖溶液期间mPFC中的细胞外多巴胺浓度。该模型将操作性实验的食欲/寻求阶段与完成阶段分开。还在未训练的处理对照组中监测多巴胺,并在EtOH饮用组中测量透析液中的EtOH。
与饮用蔗糖和处理对照组相比,经历了一周饮用甜味EtOH的大鼠的笼内基线多巴胺水平较低。与蔗糖和处理对照组相比,转移到操作性实验箱并开始消耗时,甜味EtOH组的多巴胺相对于基线有相对较高的变化。然而,所有组在转移到操作性实验箱期间均显示出多巴胺反应,并且与处理对照组相比,蔗糖组在开始消耗期间多巴胺相对于基线有相对较高的变化。在饮用EtOH的大鼠中,mPFC中多巴胺和EtOH的时间进程不同。
与对照组相比,EtOH饮用者之间细胞外mPFC多巴胺的差异表明,mPFC多巴胺参与了甜味EtOH和蔗糖的操作性自我给药机制。此外,消耗期间多巴胺的增加与mPFC多巴胺在奖励预测中的作用一致。