Leonard Michael Z, Miczek Klaus A, Covington Herbert E
Department of Psychology, Tufts University, Medford, MA, USA.
Department of Pharmacology, Vanderbilt University, Nashville, TN, USA.
Psychopharmacology (Berl). 2025 Mar;242(3):593-615. doi: 10.1007/s00213-024-06711-9. Epub 2024 Nov 8.
Anticipation is a critical antecedent to drug use, in which the prospect of imminent drug availability can potently motivate instrumental actions directed to procure it. Models that capture the behavioral dynamics that precede drug access may allow for the dissociation of key neural mechanisms underlying appetitive or consummatory processes in drug self-administration.
We aimed to isolate measurements attributed to the procurement and consumption of a reward by defining distinct actions for each using a chain-schedule of reinforcement.
Male Long-Evans rats were trained to self-administer cocaine or saccharin under a chained schedule of reinforcement (FI-FR) in order to dissociate appetitive ('seeking') from consummatory ('taking') behaviors. Completion of a fixed-interval (5 min) was followed by 5 min of continuously reinforced responding (FR1) on another lever.
The FI-FR chain procedure appears to provide sensitive and dissociable dimensions of cocaine self-administration within a single experimental session. Importantly, we demonstrate that responding during the FI (i.e., seeking) link tracks with the incentive value of anticipated reward access - whereby response rates corresponded to expected reward magnitude, degree of reward-specific satiety, and general motivational state.
The FI component is a sensitive and reliable index of motivational changes induced by either the extrinsic incentive value of reinforcement (i.e., anticipated dose) or intrinsic motive states (i.e., satiety or deprivation). This procedure provides a valuable tool for interrogating the neural dynamics of drug-seeking and -taking behavior, in isolation.
预期是药物使用的一个关键前提,在这种情况下,即将获得药物的前景能够有力地激发为获取药物而采取的工具性行动。能够捕捉药物获取之前行为动态的模型,可能有助于区分药物自我给药中食欲或满足过程背后的关键神经机制。
我们旨在通过使用强化链程序为奖励的获取和消耗定义不同的行为,来分离与奖励的获取和消耗相关的测量指标。
雄性Long-Evans大鼠在强化链程序(固定间隔-固定比率)下接受训练,以自我给药可卡因或糖精,从而将食欲性(“寻找”)行为与满足性(“摄取”)行为区分开来。在完成5分钟的固定间隔后,在另一个杠杆上进行5分钟的连续强化反应(固定比率1)。
固定间隔-固定比率链程序似乎在单个实验环节中提供了可卡因自我给药的敏感且可区分的维度。重要的是,我们证明在固定间隔(即寻找)环节的反应与预期奖励获取的激励价值相关——反应率与预期奖励大小、奖励特异性饱腹感程度和一般动机状态相对应。
固定间隔部分是由强化的外在激励价值(即预期剂量)或内在动机状态(即饱腹感或剥夺)引起的动机变化的敏感且可靠指标。该程序为单独研究药物寻找和摄取行为的神经动力学提供了一个有价值的工具。