Department of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
PLoS One. 2011 Mar 7;6(3):e17586. doi: 10.1371/journal.pone.0017586.
The neurochemical status and hyperactivity of mice lacking functional substance P-preferring NK1 receptors (NK1R-/-) resemble abnormalities in Attention Deficit Hyperactivity Disorder (ADHD). Here we tested whether NK1R-/- mice express other core features of ADHD (impulsivity and inattentiveness) and, if so, whether they are diminished by d-amphetamine, as in ADHD. Prompted by evidence that circadian rhythms are disrupted in ADHD, we also compared the performance of mice that were trained and tested in the morning or afternoon.
The 5-Choice Serial Reaction-Time Task (5-CSRTT) was used to evaluate the cognitive performance of NK1R-/- mice and their wildtypes. After training, animals were tested using a long (LITI) and a variable (VITI) inter-trial interval: these tests were carried out with, and without, d-amphetamine pretreatment (0.3 or 1 mg/kg i.p.). NK1R-/- mice expressed greater omissions (inattentiveness), perseveration and premature responses (impulsivity) in the 5-CSRTT. In NK1R-/- mice, perseveration in the LITI was increased by injection-stress but reduced by d-amphetamine. Omissions by NK1R-/- mice in the VITI were unaffected by d-amphetamine, but premature responses were exacerbated by this psychostimulant. Omissions in the VITI were higher, overall, in the morning than the afternoon but, in the LITI, premature responses of NK1R-/- mice were higher in the afternoon than the morning.
In addition to locomotor hyperactivity, NK1R-/- mice express inattentiveness, perseveration and impulsivity in the 5-CSRTT, thereby matching core criteria for a model of ADHD. Because d-amphetamine reduced perseveration in NK1R-/- mice, this action does not require functional NK1R. However, the lack of any improvement of omissions and premature responses in NK1R-/- mice given d-amphetamine suggests that beneficial effects of this psychostimulant in other rodent models, and ADHD patients, need functional NK1R. Finally, our results reveal experimental variables (stimulus parameters, stress and time of day) that could influence translational studies.
缺乏功能性 P 物质优先 NK1 受体(NK1R-/-)的小鼠的神经化学状态和多动性类似于注意力缺陷多动障碍(ADHD)的异常。在这里,我们测试了 NK1R-/-小鼠是否表达 ADHD 的其他核心特征(冲动和注意力不集中),如果是这样,它们是否会被安非他命所减弱,就像 ADHD 一样。有证据表明,昼夜节律在 ADHD 中被打乱,因此,我们还比较了在早上或下午接受训练和测试的小鼠的表现。
使用 5-选择序列反应时间任务(5-CSRTT)来评估 NK1R-/-小鼠及其野生型的认知表现。在训练后,使用长(LITI)和可变(VITI)试验间隔对动物进行测试:这些测试是在有和没有安非他命预处理(0.3 或 1mg/kg ip)的情况下进行的。NK1R-/-小鼠在 5-CSRTT 中表现出更多的遗漏(注意力不集中)、持续和过早反应(冲动)。在 NK1R-/-小鼠中,LITI 的持续反应增加了注射应激,但减少了安非他命。安非他命对 NK1R-/-小鼠 VITI 的遗漏没有影响,但对其过早反应有加剧作用。总体而言,NK1R-/-小鼠在 VITI 中的遗漏率在早上高于下午,但在 LITI 中,下午的过早反应率高于早上。
除了运动过度活跃外,NK1R-/-小鼠在 5-CSRTT 中还表现出注意力不集中、持续和冲动,从而符合 ADHD 模型的核心标准。因为安非他命减少了 NK1R-/-小鼠的持续反应,所以这种作用不需要功能性 NK1R。然而,给予安非他命后 NK1R-/-小鼠的遗漏和过早反应没有任何改善,这表明这种精神兴奋剂在其他啮齿动物模型和 ADHD 患者中的有益作用需要功能性 NK1R。最后,我们的结果揭示了可能影响转化研究的实验变量(刺激参数、应激和时间)。