Peciña Susana, Schulkin Jay, Berridge Kent C
Department of Psychology, University of Michigan, Ann Arbor, MI 48109, USA.
BMC Biol. 2006 Apr 13;4:8. doi: 10.1186/1741-7007-4-8.
Corticotropin-releasing factor (CRF) is typically considered to mediate aversive aspects of stress, fear and anxiety. However, CRF release in the brain is also elicited by natural rewards and incentive cues, raising the possibility that some CRF systems in the brain mediate an independent function of positive incentive motivation, such as amplifying incentive salience. Here we asked whether activation of a limbic CRF subsystem magnifies the increase in positive motivation for reward elicited by incentive cues previously associated with that reward, in a way that might exacerbate cue-triggered binge pursuit of food or other incentives? We assessed the impact of CRF microinjections into the medial shell of nucleus accumbens using a pure incentive version of Pavlovian-Instrumental transfer, a measure specifically sensitive to the incentive salience of reward cues (which it separates from influences of aversive stress, stress reduction, frustration and other traditional explanations for stress-increased behavior). Rats were first trained to press one of two levers to obtain sucrose pellets, and then separately conditioned to associate a Pavlovian cue with free sucrose pellets. On test days, rats received microinjections of vehicle, CRF (250 or 500 ng/0.2 microl) or amphetamine (20 microg/0.2 microl). Lever pressing was assessed in the presence or absence of the Pavlovian cues during a half-hour test.
Microinjections of the highest dose of CRF (500 ng) or amphetamine (20 microg) selectively enhanced the ability of Pavlovian reward cues to trigger phasic peaks of increased instrumental performance for a sucrose reward, each peak lasting a minute or so before decaying after the cue. Lever pressing was not enhanced by CRF microinjections in the baseline absence of the Pavlovian cue or during the presentation without a cue, showing that the CRF enhancement could not be explained as a result of generalized motor arousal, frustration or stress, or by persistent attempts to ameliorate aversive states.
We conclude that CRF in nucleus accumbens shell amplifies positive motivation for cued rewards, in particular by magnifying incentive salience that is attributed to Pavlovian cues previously associated with those rewards. CRF-induced magnification of incentive salience provides a novel explanation as to why stress may produce cue-triggered bursts of binge eating, drug addiction relapse, or other excessive pursuits of rewards.
促肾上腺皮质激素释放因子(CRF)通常被认为介导应激、恐惧和焦虑的厌恶方面。然而,大脑中CRF的释放也由自然奖励和激励线索引发,这增加了大脑中某些CRF系统介导积极激励动机独立功能的可能性,比如放大激励显著性。在这里,我们询问边缘CRF子系统的激活是否会以一种可能加剧线索触发的对食物或其他奖励的暴饮暴食的方式,放大先前与该奖励相关的激励线索所引发的对奖励的积极动机的增加?我们使用巴甫洛夫-工具性转移的纯激励版本评估了向伏隔核内侧壳微量注射CRF的影响,这是一种对奖励线索的激励显著性特别敏感的测量方法(它将奖励线索的激励显著性与厌恶应激、应激减轻、挫折以及其他对压力增加行为的传统解释的影响区分开来)。大鼠首先被训练按压两个杠杆中的一个以获得蔗糖颗粒,然后分别进行条件训练,使巴甫洛夫线索与免费蔗糖颗粒相关联。在测试日,大鼠接受载体、CRF(250或500纳克/0.2微升)或苯丙胺(20微克/0.2微升)的微量注射。在半小时的测试中,在有或没有巴甫洛夫线索的情况下评估杠杆按压情况。
最高剂量的CRF(500纳克)或苯丙胺(20微克)的微量注射选择性地增强了巴甫洛夫奖励线索触发蔗糖奖励工具性表现增加的阶段性峰值的能力,每个峰值持续约一分钟,然后在线索出现后衰减。在基线时没有巴甫洛夫线索或在没有线索呈现期间,CRF微量注射并没有增强杠杆按压,这表明CRF的增强不能用一般的运动觉醒、挫折或应激来解释,也不能用持续试图改善厌恶状态来解释。
我们得出结论,伏隔核壳中的CRF放大了对线索奖励的积极动机,特别是通过放大归因于先前与这些奖励相关的巴甫洛夫线索的激励显著性。CRF诱导的激励显著性放大为压力为何可能导致线索触发的暴饮暴食、药物成瘾复发或其他对奖励的过度追求提供了一种新的解释。