扩展获取性可卡因自我给药对成年雄性大鼠工作记忆表现、反向学习和可卡因寻找潜伏期的影响。

Journal of addiction & prevention Pub Date : 2017-04-01 Epub Date: 2017-04-27 DOI:10.13188/2330-2178.1000035
Christina Gobin, Marek Schwendt
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引用次数: 12

摘要

可卡因使用障碍的特点不仅是高复发率,而且还包括认知和前额皮质功能的缺陷。然而,认知障碍和可卡因寻求之间的关系仍然知之甚少。目前的研究使用啮齿动物模型来确定长期获取可卡因自我给药对前额叶皮层依赖性延迟匹配样本/非匹配样本(DMS/DNMS)任务中认知表现的影响。此外,本研究试图调查长期戒断后认知表现的变化与线索/情境诱导的可卡因寻求之间的关系。研究人员训练动物每天6次,每次1小时,然后是12天,每次6小时。大鼠表现出强烈的自我给药行为和可卡因摄入量的增加。然后,采用DMS/DNMS任务在0 ~ 30 s的延迟范围内评估工作记忆容量和逆向学习表现。虽然本研究未能发现主要的认知障碍,但在中等认知负荷(10 s延迟)下,长期使用可卡因会导致持续的工作记忆/DMS缺陷。逆转学习/DNMS的表现没有变化。这很可能是DMS/DNMS任务的参数,如在目前的研究中使用的,超过了大鼠的习得能力,从而在较长时间内模糊了可卡因的影响。最后,在45天的戒断后,大鼠表现出情境/线索诱导的可卡因寻求的强烈复发。然而,可卡因寻求的强度与DMS任务中的缺陷并不相关。总之,未来的研究必须重新评估在调整后的DMS/DNMS条件下,是否可以检测到可卡因后认知表现与可卡因寻求之间更强大的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Effects of Extended-Access Cocaine Self-Administration on Working Memory Performance, Reversal Learning and Incubation of Cocaine-Seeking in Adult Male Rats.

Cocaine use disorder is characterized not only by the high rate of relapse, but also by deficits in cognition and prefrontal cortical function. Still, the relationship between cognitive impairment and cocaine-seeking remains poorly understood. The current study used a rodent model to determine the effects of extended access cocaine self-administration on cognitive performance in a prefrontal cortex-dependent delayed match-to-sample/non-match-to-sample (DMS/DNMS) task. Further, this study sought to investigate how post-cocaine changes in cognitive performance correlate with cue/context-induced cocaine-seeking following a prolonged period of abstinence. Animals were trained to self-administer cocaine during 6 daily 1 hour-long sessions followed by 12 days of extended, 6 hour-long access. The extended access cocaine rats exhibited robust self-administration behavior and escalation of cocaine intake. Next, DMS/DNMS task was used to evaluate working memory capacity and reversal learning performance over a range of 0 - 30 s delays. Although this study failed to detect a major cognitive impairment, extended access to cocaine resulted in the persistent working memory/DMS deficit at a moderate cognitive load (10 s delay). There were no changes in the reversal learning/DNMS performance. It is likely that the parameters of the DMS/DNMS task, as used in the current study, exceeded acquisition capacity of rats thus obscuring cocaine effects at longer delays. Finally, rats showed a robust relapse of context/cue-elicited cocaine-seeking following the 45 - day abstinence. However, the intensity of cocaine-seeking did not correlate with the deficit in the DMS task. In conclusion, future studies must re-evaluate whether a more robust relationship between post-cocaine cognitive performance and cocaine-seeking can be detected under adjusted DMS/DNMS conditions.

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