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Single prolonged stress decreases sign-tracking and cue-induced reinstatement of cocaine-seeking

机译:单一长时间应力降低了签署追踪和提示恢复可卡因寻求的恢复

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Exposure to prolonged, uncontrollable stress reduces reward-seeking behavior, resulting in anhedonia in neuropsychiatric disorders, such as posttraumatic stress disorder. However, it is unclear to what degree stressed subjects lose interest in rewards themselves or in reward-related cues that instigate reward-seeking behavior. In the present study, we investigated the effects of single prolonged stress (SPS) on cue-directed behavior in two different procedures: Pavlovian conditioned approach (PCA) and cue-induced reinstatement of cocaine-seeking. In Experiment 1, rats were exposed to SPS and tested for the acquisition of sign-tracking (cue-directed) and goal-tracking (reward-directed) behaviors during a PCA procedure. In Experiment 2, rats were exposed to SPS and tested for the expression of sign- and goal-tracking as well as cue-induced reinstatement of cocaine-seeking. Because dopaminergic activity in the nucleus accumbens is known to play a central role in many cue-directed behaviors, including both sign-tracking and cue-induced reinstatement, Experiment 3 used in vivo microdialysis to measure the effect of SPS on baseline and evoked dopamine levels in the nucleus accumbens. SPS decreased sign-tracking and increased goal-tracking during the acquisition of PCA behavior without affecting reward consumption. In addition, SPS decreased cue-induced reinstatement without affecting cocaine self-administration. Finally, SPS decreased evoked but not baseline levels of dopamine in the nucleus accumbens. These results suggest that SPS decreases the motivational, but not consummatory, aspects of reward-seeking behavior, which may result from long-term, SPS-induced reductions in dopamine release in the nucleus accumbens.
机译:暴露在长时间,无法控制的应力降低了寻求奖励的行为,导致神经精神疾病中的Anhedonia,例如错误的应激障碍。然而,目前尚不清楚强调的受试者对自己或奖励相关提示失去兴趣的程度,以筹集奖励行为。在本研究中,我们调查了单一长长的压力(SPS)对两种不同程序中的提示行为的影响:Pavlovian条件方法(PCA)和Cue诱导的追求CoCaine恢复。在实验1中,大鼠暴露于SPS并测试在PCA程序期间获取签名跟踪(CUE指向的)和目标跟踪(奖励)行为。在实验2中,将大鼠暴露于SPS并测试表达签名和目标跟踪以及CoCaine寻求恢复的Cue-in诱导。因为核心尿嘧啶中的多巴胺能活性在许多提示的行为中发挥着核心作用,包括载体跟踪和提示诱导的恢复,实验3用于测量SPS对基线和诱发多巴胺水平的效果在核心腺中。在收购PCA行为期间,SPS在不影响奖励消费的情况下降低签字跟踪和增加的目标跟踪。此外,SPS降低了提示诱导的恢复而不影响可卡因自我给药。最后,SPS在细胞核中的诱发但不是基线水平的核心。这些结果表明,SPS降低了促进行为的励志,但没有完善的,这可能是由长期的核心释放在细胞核中的长期诱导的降低。

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