Behavioural and Clinical Neuroscience Institute, University of Cambridge, Downing Street, Cambridge, CB2 3EB, UK.
Psychopharmacology (Berl). 2011 Jun;215(4):721-31. doi: 10.1007/s00213-011-2167-x. Epub 2011 Jan 28.
Impulsivity is a vulnerability marker for drug addiction in which other behavioural traits such as anxiety and novelty seeking ('sensation seeking') are also widely present. However, inter-relationships between impulsivity, novelty seeking and anxiety traits are poorly understood.
The objective of this paper was to investigate the contribution of novelty seeking and anxiety traits to the expression of behavioural impulsivity in rats.
Rats were screened on the five-choice serial reaction time task (5-CSRTT) for spontaneously high impulsivity (SHI) and low impulsivity (SLI) and subsequently tested for novelty reactivity and preference, assessed by open-field locomotor activity (OF), novelty place preference (NPP), and novel object recognition (OR). Anxiety was assessed on the elevated plus maze (EPM) both prior to and following the administration of the anxiolytic drug diazepam, and by blood corticosterone levels following forced novelty exposure. Finally, the effects of diazepam on impulsivity and visual attention were assessed in SHI and SLI rats.
SHI rats were significantly faster to enter an open arm on the EPM and exhibited preference for novelty in the OR and NPP tests, unlike SLI rats. However, there was no dimensional relationship between impulsivity and either novelty-seeking behaviour, anxiety levels, OF activity or novelty-induced changes in blood corticosterone levels. By contrast, diazepam (0.3-3 mg/kg), whilst not significantly increasing or decreasing impulsivity in SHI and SLI rats, did reduce the contrast in impulsivity between these two groups of animals.
This investigation indicates that behavioural impulsivity in rats on the 5-CSRTT, which predicts vulnerability for cocaine addiction, is distinct from anxiety, novelty reactivity and novelty-induced stress responses, and thus has relevance for the aetiology of drug addiction.
冲动性是药物成瘾的一个脆弱性标志物,其中其他行为特征,如焦虑和寻求新奇感(“寻求刺激”)也广泛存在。然而,冲动性、寻求新奇感和焦虑特征之间的相互关系还了解甚少。
本文的目的是研究寻求新奇感和焦虑特征对大鼠行为冲动性表达的贡献。
通过 5 选择连续反应时间任务(5-CSRTT)对大鼠进行筛选,以确定其是否具有自发性高冲动性(SHI)和低冲动性(SLI),然后通过旷场运动活动(OF)、新奇位置偏好(NPP)和新颖物体识别(OR)评估其新奇反应性和偏好。在给予抗焦虑药物地西泮之前和之后,通过高架十字迷宫(EPM)评估焦虑,以及在强制新奇暴露后通过血液皮质酮水平评估焦虑。最后,评估地西泮对 SHI 和 SLI 大鼠的冲动性和视觉注意力的影响。
SHI 大鼠在 EPM 上进入开放臂的速度明显更快,并且在 OR 和 NPP 测试中表现出对新奇的偏好,而 SLI 大鼠则没有。然而,冲动性与寻求新奇感行为、焦虑水平、OF 活动或新奇诱导的血液皮质酮水平变化之间没有维度关系。相比之下,地西泮(0.3-3mg/kg)虽然没有显著增加或降低 SHI 和 SLI 大鼠的冲动性,但确实降低了这两组动物之间冲动性的差异。
本研究表明,5-CSRTT 上的大鼠行为冲动性,预测可卡因成瘾的易感性,与焦虑、寻求新奇感和新奇诱导的应激反应不同,因此与药物成瘾的病因学有关。