Department of Psychology, California State University, Los Angeles, 5151 State University Drive, Los Angeles, CA 90032, USA.
Psychopharmacology (Berl). 2012 Jan;219(2):607-20. doi: 10.1007/s00213-011-2579-7. Epub 2011 Nov 29.
Our ability to measure the cognitive components of complex decision-making across species has greatly facilitated our understanding of its neurobiological mechanisms. One task in particular, reversal learning, has proven valuable in assessing the inhibitory processes that are central to executive control. Reversal learning measures the ability to actively suppress reward-related responding and to disengage from ongoing behavior, phenomena that are biologically and descriptively related to impulsivity and compulsivity. Consequently, reversal learning could index vulnerability for disorders characterized by impulsivity such as proclivity for initial substance abuse as well as the compulsive aspects of dependence.
Though we describe common variants and similar tasks, we pay particular attention to discrimination reversal learning, its supporting neural circuitry, neuropharmacology and genetic determinants. We also review the utility of this task in measuring impulsivity and compulsivity in addictions.
We restrict our review to instrumental, reward-related reversal learning studies as they are most germane to addiction.
The research reviewed here suggests that discrimination reversal learning may be used as a diagnostic tool for investigating the neural mechanisms that mediate impulsive and compulsive aspects of pathological reward-seeking and -taking behaviors. Two interrelated mechanisms are posited for the neuroadaptations in addiction that often translate to poor reversal learning: frontocorticostriatal circuitry dysregulation and poor dopamine (D2 receptor) modulation of this circuitry. These data suggest new approaches to targeting inhibitory control mechanisms in addictions.
我们在跨物种层面上衡量复杂决策的认知成分的能力极大地促进了我们对其神经生物学机制的理解。特别是,反转学习任务在评估对执行控制至关重要的抑制过程方面非常有价值。反转学习衡量的是主动抑制与奖励相关的反应并脱离正在进行的行为的能力,这些现象在生物学和描述上与冲动性和强迫性有关。因此,反转学习可以指示易患冲动性障碍的脆弱性,例如初始物质滥用的倾向以及依赖的强迫性方面。
虽然我们描述了常见的变体和类似的任务,但我们特别关注辨别反转学习、其支持的神经回路、神经药理学和遗传决定因素。我们还回顾了该任务在衡量成瘾中的冲动性和强迫性方面的效用。
我们将综述限制在与成瘾最相关的工具性、奖励相关的反转学习研究中。
这里回顾的研究表明,辨别反转学习可以用作研究介导病理性奖励寻求和获取行为的冲动和强迫性方面的神经机制的诊断工具。假设了两种相互关联的机制来解释成瘾中的神经适应性,这些适应性通常转化为较差的反转学习:前皮质纹状体回路失调和多巴胺(D2 受体)对该回路的调节不良。这些数据表明了针对成瘾中的抑制控制机制的新方法。