Behavioral Neuroscience Branch, IRP/NIDA/NIH, Baltimore, MD, USA.
Center for Social and Affective Neuroscience, Linköping University, Linköping, Sweden.
Curr Opin Neurobiol. 2024 Jun;86:102856. doi: 10.1016/j.conb.2024.102856. Epub 2024 Mar 19.
Relapse to drug use during abstinence is a defining feature of addiction. To date, however, results from studies using rat relapse/reinstatement models have yet to result in FDA-approved medications for relapse prevention. To address this translational gap, we and others have developed rat models of relapse after voluntary abstinence from drug self-administration. One of these models is the electric barrier conflict model. Here, we introduce the model, and then review studies on behavioral and neuropharmacological mechanisms of cue-induced relapse and incubation of drug seeking (time-dependent increase in drug seeking during abstinence) after electric barrier-induced abstinence. We also briefly discuss future directions and potential clinical implications. One major conclusion of our review is that the brain mechanisms controlling drug relapse after electrical barrier-induced voluntary abstinence are likely distinct from those controlling relapse after homecage forced abstinence.
在戒断期间重新使用毒品是成瘾的一个定义性特征。然而,迄今为止,使用大鼠复吸/复本位模型进行的研究结果尚未导致用于预防复吸的 FDA 批准药物。为了解决这一转化差距,我们和其他人已经开发了大鼠自愿戒断药物自我给药后的复吸模型。其中一种模型是电动障碍冲突模型。在这里,我们介绍了该模型,然后回顾了关于线索诱导复吸和药物寻求潜伏期(戒断期间药物寻求的时间依赖性增加)的行为和神经药理学机制的研究,这些研究是在电动障碍诱导戒断后进行的。我们还简要讨论了未来的方向和潜在的临床意义。我们的综述得出的一个主要结论是,控制电击诱导自愿戒断后药物复吸的大脑机制可能与控制笼内强制戒断后药物复吸的大脑机制不同。