Dimet Andrea L, Cisneros Irma E, Fox Robert G, Stutz Sonja J, Anastasio Noelle C, Cunningham Kathryn A, Dineley Kelly T
Center for Addiction Research, University of Texas Medical Branch; Institute for Translational Sciences, University of Texas Medical Branch; Mitchell Center for Neurodegenerative Diseases, University of Texas Medical Branch.
Center for Addiction Research, University of Texas Medical Branch; Department of Neurology, University of Texas Medical Branch; Department of Pathology, University of Texas Medical Branch.
J Vis Exp. 2018 Jun 18(136):55864. doi: 10.3791/55864.
Cocaine use disorder (CUD) follows a trajectory of repetitive self-administration during which previously neutral stimuli gain incentive value. Cue reactivity, the sensitivity to cues previously linked with the drug-taking experience, plays a prominent role in human craving during abstinence. Cue reactivity can be assessed as the attentional orientation toward drug-associated cues that is measurable as appetitive approach behavior in both preclinical and human studies. Herein describes an assessment of cue reactivity in rats trained to self-administer cocaine. Cocaine self-administration is paired with the presentation of discrete cues that act as conditioned reinforcers (i.e., house light, stimulus light, infusion pump sounds). Following a period of abstinence, lever presses in the cocaine self-administration context accompanied by the discrete cues previously paired with cocaine infusion are measured as cue reactivity. This model is useful to explore neurobiological mechanisms underlying cue reactivity processes as well as to assess pharmacotherapies to suppress cue reactivity and therefore, modify relapse vulnerability. Advantages of the model include its translational relevance, and its face and predictive validities. The primary limitation of the model is that the cue reactivity task can only be performed infrequently and must only be used in short duration (e.g., 1 hour), otherwise rats will begin to extinguish the pairing of the discrete cues with the cocaine stimulus. The model is extendable to any positively reinforcing stimulus paired with discrete cues; though particularly applicable to drugs of abuse, this model may hold future applications in fields such as obesity, where palatable food rewards can act as positively reinforcing stimuli.
可卡因使用障碍(CUD)遵循重复自我给药的轨迹,在此过程中,先前的中性刺激获得了激励价值。线索反应性,即对先前与吸毒经历相关线索的敏感性,在禁欲期间的人类渴望中起着重要作用。线索反应性可以被评估为对与药物相关线索的注意力定向,在临床前和人类研究中,这种定向可作为食欲趋近行为来测量。本文描述了对经训练自我给药可卡因的大鼠的线索反应性评估。可卡因自我给药与充当条件强化物的离散线索(即饲养箱灯、刺激光、输液泵声音)的呈现配对。在一段禁欲期后,在可卡因自我给药环境中伴随先前与可卡因输注配对的离散线索的杠杆按压被测量为线索反应性。该模型有助于探索线索反应性过程背后的神经生物学机制,以及评估抑制线索反应性从而改变复发易感性的药物治疗方法。该模型的优点包括其转化相关性、表面效度和预测效度。该模型的主要局限性在于线索反应性任务只能不频繁地进行,并且必须仅在短时间内(例如1小时)使用,否则大鼠将开始消除离散线索与可卡因刺激的配对。该模型可扩展到与离散线索配对的任何正性强化刺激;尽管特别适用于滥用药物,但该模型可能在肥胖等领域有未来应用,在肥胖领域中,美味的食物奖励可作为正性强化刺激。