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Cue-Evoked Cocaine Craving: Role of Dopamine in the Accumbens Core

机译:提示诱发可卡因的渴望:多巴胺在Accumbens核心中的作用

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摘要

Drug-associated cues can acquire powerful motivational control over the behavior of addicts, and can contribute to relapse via multiple, dissociable mechanisms. Most preclinical models of relapse focus on only one of these mechanisms: the ability of drug cues to reinforce drug-seeking actions following a period of extinction training. However, in addicts, drug cues typically do not follow seeking actions; they precede them. They often produce relapse by evoking a conditioned motivational state (“wanting” or “craving”) that instigates and/or invigorates drug-seeking behavior. Here we used a conflict-based relapse model to ask whether individual variation in the propensity to attribute incentive salience to reward cues predicts variation in the ability of a cocaine cue to produce conditioned motivation (craving) for cocaine. Following self-administration training, responding was curtailed by requiring rats to cross an electrified floor to take cocaine. The subsequent response-independent presentation of a cocaine-associated cue was sufficient to reinstate drug-seeking behavior, despite the continued presence of the adverse consequence. Importantly, there were large individual differences in the motivational properties of the cocaine cue, which were predicted by variation in the propensity to attribute incentive salience to a food cue. Finally, a dopamine antagonist injected into the nucleus accumbens core attenuated, and amphetamine facilitated, cue-evoked cocaine seeking, implicating dopamine signaling in cocaine cue-evoked craving. These data provide a promising preclinical approach for studying sources of individual variation in susceptibility to relapse due to conditioned craving and implicate mesolimbic dopamine in this process.
机译:与毒品有关的线索可以对成瘾者的行为进行强有力的动机控制,并可以通过多种可分离的机制促进复发。大多数临床前复发模型仅关注以下机制之一:经过一段时间的灭绝训练后,药物提示增强了寻求药物的作用的能力。但是,在吸毒者中,吸毒线索通常不遵循寻求行动;他们先于他们。它们通常通过激发条件性动机状态(“想要”或“渴望”)而引起复发,从而激发和/或激发寻求毒品的行为。在这里,我们使用基于冲突的复发模型来询问将动机显着性归因于奖励线索的倾向中的个体变化是否预测了可卡因线索产生可卡因的条件动机(渴望)的能力的变化。经过自我管理训练后,要求大鼠越过带电地板服用可卡因,从而减少了反应。尽管持续存在不良后果,但随后可卡因相关提示的独立于反应的提示足以恢复药物寻找行为。重要的是,可卡因提示的动机性质存在很大的个体差异,这是通过将诱因显着性归因于食物提示的倾向的变化来预测的。最后,注射到伏隔核核心的多巴胺拮抗剂减弱,苯丙胺促进提示诱发可卡因的寻找,将多巴胺信号传导牵涉可卡因提示诱发的渴望。这些数据提供了一种有前途的临床前方法,用于研究因条件渴望而导致的复发易感性个体差异的来源,并在此过程中牵涉中脑边缘多巴胺。

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