Vanderschuren Louk J M J, Pierce R Christopher
Department of Neuroscience and Pharmacology, University Medical Center Utrecht, Utrecht, The Netherlands.
Curr Top Behav Neurosci. 2010;3:179-95. doi: 10.1007/7854_2009_21.
In 1993, Robinson and Berridge published their first review that laid out the incentive sensitization theory of addiction (Robinson and Berridge 1993 Brain Res Rev 18:247). Its basic point is that repeated exposure to drugs of abuse causes hypersensitivity to drugs and drug-associated stimuli of the neural circuits mediating incentive salience, an important way in which motivational stimuli influence behavior. In laymen's terms, it states that this drug-induced hypersensitivity of motivational circuitry would mediate an increase in drug "wanting," thus being responsible for the dramatically exaggerated motivation for drugs displayed by addicts. This theory has been exceptionally influential, as evidenced by the fact that the original review paper about this theory (Robinson and Berridge 1993 Brain Res Rev 18:247) has been cited 2,277 times so far, and subsequent updates of this view (Robinson and Berridge 2000 Addiction 95(Suppl 2):S91; Robinson and Berridge 2001 Addiction 96:103; Robinson and Berridge 2003 Ann Rev Psychol 54:25) have been cited 274, 297, and 365 times, respectively, adding up to more than 3,200 citations within 15 years. The present chapter aims to delineate the merits and limitations of the incentive sensitization view of addiction, and whether incentive sensitization occurs in humans. We conclude that since incentive sensitization most prominently occurs after the first few drug exposures, it may represent an important initial step in the addiction process. During the expression of full-blown addiction, characterized by loss of control over drug intake and use of large quantities of drugs, the expression of incentive sensitization may be transiently suppressed. However, detoxification and the gradual disappearance of tolerance and withdrawal symptoms may unmask sensitization, which could then play an important role in the high risk of relapse.
1993年,罗宾逊和贝里奇发表了他们的第一篇综述,阐述了成瘾的动机敏感化理论(罗宾逊和贝里奇,1993年,《脑研究回顾》18:247)。其基本观点是,反复接触滥用药物会导致对药物以及介导动机显著性的神经回路中与药物相关的刺激产生超敏反应,这是动机刺激影响行为的一种重要方式。用通俗的话说,该理论认为这种由药物引起的动机回路超敏反应会介导药物“渴望”的增加,从而导致成瘾者对药物表现出极度夸张的动机。这一理论极具影响力,事实证明,关于该理论的原始综述论文(罗宾逊和贝里奇,1993年,《脑研究回顾》18:247)截至目前已被引用2277次,而该观点的后续更新(罗宾逊和贝里奇,2000年,《成瘾》95(增刊2):S91;罗宾逊和贝里奇,2001年,《成瘾》96:103;罗宾逊和贝里奇,2003年,《心理学年度评论》54:25)分别被引用274次、297次和365次,15年内累计引用超过3200次。本章旨在阐述成瘾的动机敏感化观点的优点和局限性,以及动机敏感化是否在人类身上发生。我们得出的结论是,由于动机敏感化最显著地发生在最初几次药物接触之后,它可能代表成瘾过程中的一个重要初始步骤。在全面成瘾表现为对药物摄入失去控制并大量使用药物的阶段,动机敏感化的表现可能会被暂时抑制。然而,戒毒以及耐受性和戒断症状的逐渐消失可能会使敏感化显现出来,进而在高复发风险中发挥重要作用。