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精神运动性敏感与强迫性可卡因消费的分离。

Dissociation of psychomotor sensitization from compulsive cocaine consumption.

作者信息

Ahmed Serge H, Cador Martine

机构信息

Laboratoire de Neuropsychobiologie des Désadaptations, University Victor-Segalen Bordeaux2, Bordeaux, France.

出版信息

Neuropsychopharmacology. 2006 Mar;31(3):563-71. doi: 10.1038/sj.npp.1300834.

Abstract

The transition from drug use to drug addiction is associated with a process of escalation, whereby drug use becomes excessive and difficult to control. Several mechanisms have been advanced to explain escalating patterns of drug use as opposed to nonescalating patterns. Although current evidence favors hedonic tolerance, there remains some dispute about the contribution of behavioral sensitization to cocaine intake escalation. Here, we concurrently assessed the ability of cocaine to induce psychomotor sensitization and drug-seeking behavior in animals with 1-h (short access or ShA) vs 6-h (long access or LgA) access to intravenous (i.v.) cocaine self-administration. As expected, cocaine intake by LgA rats escalated over time and became excessive compared to cocaine intake by ShA rats, which remained low and stable. Despite escalated levels of cocaine consumption, however, LgA rats were not more sensitized to cocaine than ShA rats. The dose-effect function for cocaine-induced locomotion (0.125-1 mg, i.v.) was shifted to the left in LgA rats by the same amount as in ShA rats after cocaine self-administration. In contrast, LgA rats were much more responsive than ShA rats to the motivational effects of cocaine, as measured by the ability of i.v. cocaine to reinstate extinguished drug-seeking behavior. This study demonstrates a dissociation of psychomotor sensitization from the change in motivation underlying the transition to compulsive cocaine consumption, and therefore suggests that responsiveness to the motivational effects of the drug, not psychomotor sensitization, would represent a specific behavioral marker of the transition to and maintenance of compulsive cocaine use.

摘要

从药物使用到药物成瘾的转变与一个剂量增加的过程相关,在此过程中药物使用变得过度且难以控制。已经提出了几种机制来解释药物使用的剂量增加模式与非剂量增加模式的差异。尽管目前的证据支持享乐耐受,但关于行为敏化对可卡因摄入量增加的作用仍存在一些争议。在这里,我们同时评估了可卡因在动物中诱导精神运动敏化和觅药行为的能力,这些动物分别有1小时(短给药时间或ShA)和6小时(长给药时间或LgA)的静脉注射可卡因自我给药时间。正如预期的那样,与保持低水平且稳定的ShA大鼠的可卡因摄入量相比,LgA大鼠的可卡因摄入量随时间增加并变得过度。然而,尽管可卡因消费水平升高,但LgA大鼠对可卡因的敏化程度并不比ShA大鼠更高。在可卡因自我给药后,LgA大鼠中可卡因诱导运动(静脉注射0.125 - 1毫克)的剂量 - 效应函数与ShA大鼠一样向左移动相同的量。相比之下,通过静脉注射可卡因恢复消退的觅药行为的能力来衡量,LgA大鼠对可卡因的动机效应比ShA大鼠更敏感。这项研究表明,精神运动敏化与向强迫性可卡因消费转变背后的动机变化相分离,因此表明对药物动机效应的反应性而非精神运动敏化,将代表向强迫性可卡因使用转变和维持的特定行为标志物。

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