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审前可卡因通过抑制非药物选择使个体偏向可卡因选择。

Pre-trial cocaine biases choice toward cocaine through suppression of the nondrug option.

机构信息

Laboratory of Neuropsychopharmacology, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.

Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, 146 rue Léo-Saignat, F-33000 Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, 146 rue Léo-Saignat, F-33000 Bordeaux, France.

出版信息

Pharmacol Biochem Behav. 2018 Oct;173:65-73. doi: 10.1016/j.pbb.2018.07.010. Epub 2018 Jul 27.

Abstract

Being under the influence during choice between drug and nondrug options can have a dramatic effect on choice outcomes. When rats face a choice between cocaine and sweet water and are not under the influence, they prefer sweet water. In contrast, when they are under the influence of cocaine, this causes them to shift their choice to cocaine nearly exclusively. Here we sought to characterize the behavioral mechanisms underlying the influence of cocaine on choice. In theory, rats under the influence of cocaine should be in a mixed motivational state, at least temporarily, with both their motivation for cocaine and their motivation for the nondrug option suppressed by the drug satiating and anorexic effects of cocaine, respectively. For this mixed state to shift choice to cocaine, the satiated motivation for cocaine should recover before the suppressed motivation for the preferred nondrug option. The goal of the present study was to test this prediction in rats that expressed a preference for sweet water after extended access to cocaine self-administration. We measured their choice and response latencies to each option after pre-trial, passive administration of cocaine to estimate the duration of its drug satiating and anorexic effects. As expected, pre-trial cocaine caused most rats to shift their choice to cocaine. Though this shift was not simply due to a longer latency to respond for sweet water than for cocaine after pre-trial cocaine, it nevertheless occurred while rats' motivation for the nondrug option was still partially suppressed. Thus, cocaine seems to bias choice toward more cocaine mainly via suppression of the nondrug option.

摘要

在药物和非药物选择之间,受药物影响会对选择结果产生巨大影响。当老鼠面对可卡因和甜水之间的选择,并且不受影响时,它们更喜欢甜水。相比之下,当它们受到可卡因的影响时,这会导致它们几乎完全转向可卡因。在这里,我们试图描述可卡因对选择的影响背后的行为机制。从理论上讲,受可卡因影响的老鼠应该处于一种混合的动机状态,至少是暂时的,它们对可卡因的动机和对非药物选择的动机都被可卡因的饱腹感和厌食作用分别抑制。为了使这种混合状态将选择转向可卡因,可卡因的饱腹感动机应该在被抑制的对首选非药物选择的动机之前恢复。本研究的目的是在经过长期可卡因自我给药后表现出对甜水偏好的老鼠中测试这一预测。我们测量了它们在每个选项前的可卡因被动给药后的选择和反应潜伏期,以估计可卡因的饱腹感和厌食作用的持续时间。正如预期的那样,预试可卡因导致大多数老鼠将选择转向可卡因。尽管这种转变并不是仅仅由于预试可卡因后对甜水的反应潜伏期比可卡因长,但它仍然发生在老鼠对非药物选择的动机仍部分被抑制的时候。因此,可卡因似乎主要通过抑制非药物选择来偏向选择更多的可卡因。

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