Nikiforuk Agnieszka, Kalaba Predrag, Ilic Marija, Korz Volker, Dragačević Vladimir, Wackerlig Judith, Langer Thierry, Höger Harald, Golebiowska Joanna, Popik Piotr, Lubec Gert
Department of Behavioral Neuroscience and Drug Development, Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Department of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Front Behav Neurosci. 2017 Nov 27;11:222. doi: 10.3389/fnbeh.2017.00222. eCollection 2017.
Reduced cognitive abilities are often characterized by an impairment of flexibility, i.e., the ability to switch from learned rules or categories that were important in certain contexts to different new modalities that rule the task. Drugs targeting the dopamine transporter (DAT) are widely used for their potential to enhance cognitive abilities. However, commercially available drugs are of limited specificity for DAT, blocking also noradrenaline and serotonine transporters, that can lead to unwanted side effects in healthy subjects. Therefore, we tested a newly synthetized compound (CE-123) with higher specificity for DAT in male rats in an attentional set-shifting task (ASST), that proves for cognitive flexibility and a 5-choice serial-reaction time task (5-CSRTT) assessing visuospatial attention and impulsivity. Treated rats at a dose of 0.3 and 1.0 but not 0.1 mg/kg bodyweight showed reduced extra-dimensional shifts in the ASST compared to controls indicating increased cognitive flexibility. Rats treated with R-Modafinil, a commercially available DAT inhibitor at a dose of 10 mg/kg bodyweight showed increased premature responses, an indicator of increased impulsivity, during a 10 s but not a 2.5, 5, or 7.5 s intertrial interval when compared to vehicle-treated rats in the 5-CSRTT. This was not found in rats treated with CE-123 at the same dose as for R-Modafinil. Visuospatial attention, except premature responses, did not differ between R-Modafinil and CE-123-treated rats and their respective controls. Thus, CE-123 increased cognitive flexibility with diminished impulsivity.
认知能力下降通常表现为灵活性受损,即从在某些情境中重要的已学规则或类别转换到支配任务的不同新模式的能力受损。靶向多巴胺转运体(DAT)的药物因其增强认知能力的潜力而被广泛使用。然而,市售药物对DAT的特异性有限,还会阻断去甲肾上腺素和5-羟色胺转运体,这可能会在健康受试者中导致不良副作用。因此,我们在雄性大鼠的注意力转换任务(ASST)中测试了一种对DAT具有更高特异性的新合成化合物(CE-123),该任务可证明认知灵活性,还测试了一种评估视觉空间注意力和冲动性的5选串行反应时间任务(5-CSRTT)。与对照组相比,以0.3和1.0mg/kg体重剂量治疗的大鼠在ASST中维度外转换减少,表明认知灵活性增加。在5-CSRTT中,与用赋形剂处理的大鼠相比,以10mg/kg体重剂量使用市售DAT抑制剂R-莫达非尼治疗的大鼠在10秒而非2.5、5或7.5秒的试验间隔期间过早反应增加,这是冲动性增加的一个指标。在用与R-莫达非尼相同剂量的CE-123治疗的大鼠中未发现这种情况。除过早反应外,R-莫达非尼和CE-123治疗的大鼠及其各自的对照组之间视觉空间注意力没有差异。因此,CE-123增加了认知灵活性,同时减少了冲动性。