Behavioral Neuroscience Research Branch, National Institute on Drug Abuse, National Institutes of Health, United States Department of Health and Human Services, Baltimore, Maryland, United States of America.
PLoS One. 2010 Jan 15;5(1):e8741. doi: 10.1371/journal.pone.0008741.
Administration of psychomotor stimulants like amphetamine facilitates behavior in the presence of incentive distal stimuli, which have acquired the motivational properties of primary rewards through associative learning. This facilitation appears to be mediated by the mesolimbic dopamine system, which may also be involved in facilitating behavior in the presence of distal stimuli that have not been previously paired with primary rewards. However, it is unclear whether psychomotor stimulants facilitate behavioral interaction with unconditioned distal stimuli.
We found that noncontingent administration of amphetamine into subregions of the rat ventral striatum, particularly in the vicinity of the medial olfactory tubercle, facilitates lever pressing followed by visual signals that had not been paired with primary rewards. Noncontingent administration of amphetamine failed to facilitate lever pressing when it was followed by either tones or delayed presentation or absence of visual signals, suggesting that visual signals are key for enhanced behavioral interaction. Systemic administration of amphetamine markedly increased locomotor activity, but did not necessarily increase lever pressing rewarded by visual signals, suggesting that lever pressing is not a byproduct of heightened locomotor activity. Lever pressing facilitated by amphetamine was reduced by co-administration of the dopamine receptor antagonists SCH 23390 (D1 selective) or sulpiride (D2 selective).
Our results suggest that amphetamine administration into the ventral striatum, particularly in the vicinity of the medial olfactory tubercle, activates dopaminergic mechanisms that strongly enhance behavioral interaction with unconditioned visual stimuli.
施用苯丙胺等精神兴奋剂可促进在激励性远端刺激物存在下的行为,这些刺激物通过联想学习获得了主要奖励的动机特性。这种促进作用似乎是由中脑边缘多巴胺系统介导的,该系统也可能参与促进存在未与主要奖励配对的远端刺激物存在下的行为。然而,目前尚不清楚精神兴奋剂是否促进与未条件化的远端刺激物的行为相互作用。
我们发现,非条件性地将安非他命注入大鼠腹侧纹状体的亚区,特别是在靠近内侧嗅结节的地方,会促进在视觉信号之后的杠杆按压,而这些信号之前没有与主要奖励配对。非条件性给予安非他命不能促进在跟随音调和延迟呈现或没有视觉信号时的杠杆按压,这表明视觉信号是增强行为相互作用的关键。安非他命的全身给药显著增加了运动活动,但不一定增加了由视觉信号奖励的杠杆按压,这表明杠杆按压不是运动活动增强的副产物。安非他命促进的杠杆按压减少了多巴胺受体拮抗剂 SCH 23390(D1 选择性)或硫必利(D2 选择性)的共同给药。
我们的结果表明,安非他命在腹侧纹状体中的给药,特别是在靠近内侧嗅结节的地方,激活了多巴胺能机制,这些机制强烈增强了与未条件化的视觉刺激的行为相互作用。