Goldstein Rita Z, Volkow Nora D
Medical Research, Brookhaven National Laboratory, Bldg. 490, 30 Bell Avenue, Upton, NY 11973, USA.
Am J Psychiatry. 2002 Oct;159(10):1642-52. doi: 10.1176/appi.ajp.159.10.1642.
Studies of the neurobiological processes underlying drug addiction primarily have focused on limbic subcortical structures. Here the authors evaluated the role of frontal cortical structures in drug addiction.
An integrated model of drug addiction that encompasses intoxication, bingeing, withdrawal, and craving is proposed. This model and findings from neuroimaging studies on the behavioral, cognitive, and emotional processes that are at the core of drug addiction were used to analyze the involvement of frontal structures in drug addiction.
The orbitofrontal cortex and the anterior cingulate gyrus, which are regions neuroanatomically connected with limbic structures, are the frontal cortical areas most frequently implicated in drug addiction. They are activated in addicted subjects during intoxication, craving, and bingeing, and they are deactivated during withdrawal. These regions are also involved in higher-order cognitive and motivational functions, such as the ability to track, update, and modulate the salience of a reinforcer as a function of context and expectation and the ability to control and inhibit prepotent responses.
These results imply that addiction connotes cortically regulated cognitive and emotional processes, which result in the overvaluing of drug reinforcers, the undervaluing of alternative reinforcers, and deficits in inhibitory control for drug responses. These changes in addiction, which the authors call I-RISA (impaired response inhibition and salience attribution), expand the traditional concepts of drug dependence that emphasize limbic-regulated responses to pleasure and reward.
药物成瘾潜在神经生物学过程的研究主要集中在边缘系统皮质下结构。本文作者评估了额叶皮质结构在药物成瘾中的作用。
提出了一个涵盖中毒、暴饮暴食、戒断和渴望的药物成瘾综合模型。该模型以及关于药物成瘾核心行为、认知和情感过程的神经影像学研究结果被用于分析额叶结构在药物成瘾中的参与情况。
眶额皮质和前扣带回,这两个在神经解剖学上与边缘结构相连的区域,是最常与药物成瘾相关的额叶皮质区域。它们在成瘾者中毒、渴望和暴饮暴食期间被激活,而在戒断期间则被抑制。这些区域还参与高阶认知和动机功能,例如根据情境和期望追踪、更新和调节强化物显著性的能力,以及控制和抑制优势反应的能力。
这些结果表明,成瘾意味着皮质调节的认知和情感过程,这导致对药物强化物的过度重视、对替代强化物的轻视以及对药物反应的抑制控制缺陷。作者将成瘾中的这些变化称为I-RISA(反应抑制和显著性归因受损),扩展了传统的药物依赖概念,传统概念强调边缘系统对愉悦和奖励的调节反应。