Robinson T E, Berridge K C
Department of Psychology, University of Michigan, Ann Arbor 48104-1687.
Brain Res Brain Res Rev. 1993 Sep-Dec;18(3):247-91. doi: 10.1016/0165-0173(93)90013-p.
This paper presents a biopsychological theory of drug addiction, the 'Incentive-Sensitization Theory'. The theory addresses three fundamental questions. The first is: why do addicts crave drugs? That is, what is the psychological and neurobiological basis of drug craving? The second is: why does drug craving persist even after long periods of abstinence? The third is whether 'wanting' drugs (drug craving) is attributable to 'liking' drugs (to the subjective pleasurable effects of drugs)? The theory posits the following. (1) Addictive drugs share the ability to enhance mesotelencephalic dopamine neurotransmission. (2) One psychological function of this neural system is to attribute 'incentive salience' to the perception and mental representation of events associated with activation of the system. Incentive salience is a psychological process that transforms the perception of stimuli, imbuing them with salience, making them attractive, 'wanted', incentive stimuli. (3) In some individuals the repeated use of addictive drugs produces incremental neuroadaptations in this neural system, rendering it increasingly and perhaps permanently, hypersensitive ('sensitized') to drugs and drug-associated stimuli. The sensitization of dopamine systems is gated by associative learning, which causes excessive incentive salience to be attributed to the act of drug taking and to stimuli associated with drug taking. It is specifically the sensitization of incentive salience, therefore, that transforms ordinary 'wanting' into excessive drug craving. (4) It is further proposed that sensitization of the neural systems responsible for incentive salience ('for wanting') can occur independently of changes in neural systems that mediate the subjective pleasurable effects of drugs (drug 'liking') and of neural systems that mediate withdrawal. Thus, sensitization of incentive salience can produce addictive behavior (compulsive drug seeking and drug taking) even if the expectation of drug pleasure or the aversive properties of withdrawal are diminished and even in the face of strong disincentives, including the loss of reputation, job, home and family. We review evidence for this view of addiction and discuss its implications for understanding the psychology and neurobiology of addiction.
本文提出了一种关于药物成瘾的生物心理学理论——“动机-敏化理论”。该理论探讨了三个基本问题。第一个问题是:为什么成瘾者会渴望药物?也就是说,药物渴望的心理和神经生物学基础是什么?第二个问题是:为什么即使经过长时间的戒断,药物渴望仍然持续存在?第三个问题是,对药物的“想要”(药物渴望)是否归因于对药物的“喜欢”(药物的主观愉悦效果)?该理论假定如下。(1)成瘾性药物具有增强中脑边缘多巴胺神经传递的能力。(2)该神经系统的一个心理功能是将“动机显著性”赋予与该系统激活相关的事件的感知和心理表征。动机显著性是一个心理过程,它改变对刺激的感知,使其具有显著性,使其具有吸引力、“被想要”,成为激励性刺激。(3)在一些个体中,成瘾性药物的反复使用会在这个神经系统中产生渐进性的神经适应性变化,使其对药物和与药物相关的刺激越来越敏感(“敏化”),甚至可能永久敏感。多巴胺系统的敏化是由联想学习控制的,这会导致过度的动机显著性被归因于药物摄取行为和与药物摄取相关的刺激。因此,正是动机显著性的敏化将普通的“想要”转变为过度的药物渴望。(4)进一步提出,负责动机显著性(“想要”)的神经系统的敏化可以独立于介导药物主观愉悦效果(药物“喜欢”)的神经系统和介导戒断的神经系统的变化而发生。因此,即使对药物愉悦的预期或戒断的厌恶特性减弱,甚至面对包括声誉、工作、家庭和家人丧失在内的强烈抑制因素,动机显著性的敏化也会产生成瘾行为(强迫性觅药和用药)。我们回顾了支持这种成瘾观点的证据,并讨论了其对理解成瘾的心理学和神经生物学的意义。