Pope Derek A, Boomhower Steven R, Hutsell Blake A, Teixeira Kathryn M, Newland M Christopher
Auburn University, Auburn, AL, USA.
Virginia Commonwealth University, Richmond, VA, USA.
Neurobiol Learn Mem. 2016 Apr;130:93-104. doi: 10.1016/j.nlm.2016.01.017. Epub 2016 Feb 8.
Adolescence is marked by the continued development of the neural pathways that support choice and decision-making, particularly those involving dopamine signaling. Cocaine exposure during adolescence may interfere with this development and manifest as increased perseveration and delay discounting in adulthood, behavioral processes that are related to drug addiction. Adolescent mice were exposed to 30mg/kg/day of cocaine (n=11) or saline vehicle (n=10) for 14days and behavior was assessed in adulthood. In Experiment 1, performance on a spatial-discrimination-reversal procedure was evaluated. In the first two sessions following the first reversal, cocaine-exposed mice produced more preservative errors relative to controls. In Experiment 2, cocaine-exposed mice displayed steeper delay discounting than saline-exposed mice, effects that were reversed by acute cocaine administration. Experiment 3 examined responding maintained by a range of fixed-ratio schedules of reinforcement. An analysis based on a theoretical framework called Mathematical Principles of Reinforcement (MPR) was applied to response-rate functions of individual mice. According to MPR, differences in response-rate functions in adulthood were due to a steepening of the delay-of-reinforcement gradient, disrupted motoric capacity (lower maximum response rates), and enhanced reinforcer efficacy for the adolescent cocaine- compared with saline-exposed mice. Overall, these experiments suggest that chronic exposure to cocaine during adolescence may impair different features of 'executive functions' in adulthood, and these may be related to distortions in the impact of reinforcing events.
青春期的标志是支持选择和决策的神经通路持续发育,尤其是那些涉及多巴胺信号传导的通路。青春期接触可卡因可能会干扰这种发育,并在成年后表现为持续性增加和延迟折扣增加,这些行为过程与药物成瘾有关。将青春期小鼠每天暴露于30mg/kg的可卡因(n = 11)或生理盐水(n = 10)中,持续14天,并在成年后评估其行为。在实验1中,评估了空间辨别反转程序的表现。在第一次反转后的前两个实验环节中,接触可卡因的小鼠相对于对照组产生了更多的持续性错误。在实验2中,接触可卡因的小鼠比接触生理盐水的小鼠表现出更陡峭的延迟折扣,急性给予可卡因可逆转这些效应。实验3研究了由一系列固定比率强化程序维持的反应。基于一个名为“强化数学原理”(MPR)的理论框架对个体小鼠的反应率函数进行了分析。根据MPR,成年后反应率函数的差异是由于强化延迟梯度变陡、运动能力受损(最大反应率较低)以及与接触生理盐水的小鼠相比,青春期接触可卡因的小鼠强化物效力增强。总体而言,这些实验表明,青春期长期接触可卡因可能会损害成年期“执行功能”的不同特征,这些可能与强化事件影响的扭曲有关。