首页> 美国卫生研究院文献>Frontiers in Behavioral Neuroscience >A Novel Dopamine Transporter Inhibitor CE-123 Improves Cognitive Flexibility and Maintains Impulsivity in Healthy Male Rats
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A Novel Dopamine Transporter Inhibitor CE-123 Improves Cognitive Flexibility and Maintains Impulsivity in Healthy Male Rats

机译:新型多巴胺转运蛋白抑制剂CE-123可改善健康雄性大鼠的认知灵活性并保持冲动

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摘要

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.
机译:认知能力下降通常表现为灵活性受损,即从某些情况下重要的学习规则或类别切换为统治任务的不同新模式的能力。针对多巴胺转运蛋白(DAT)的药物因其增强认知能力的潜力而被广泛使用。但是,市售药物对DAT的特异性有限,还会阻断去甲肾上腺素和5-羟色胺转运蛋白,在健康受试者中可能导致不良副作用。因此,我们在注意力定移任务(ASST)中测试了对雄性大鼠DAT具有更高特异性的新合成化合物(CE-123),该化合物证明了认知灵活性和5选择系列反应时间任务(5- CSRTT)评估视觉空间注意力和冲动性。与对照组相比,剂量为0.3和1.0但不是0.1 mg / kg体重的治疗大鼠显示ASST的维度外移动减少,表明对照组的认知灵活性增强。与市售的DAT抑制剂R-莫达非尼(10 mg / kg体重)相比,大鼠在10 s间隔但不2.5、5或7.5 s间隔期间显示出过早反应增加,这是冲动性的指示,在5-CSRTT中接受媒介物处理的大鼠。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。在R-莫达非尼和CE-123治疗的大鼠及其相应的对照组之间,除早反应外,视觉空间注意力没有差异。因此,CE-123增加了认知灵活性,而冲动性却有所降低。

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