Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, 30912, Georgia.
Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, 30912, Georgia.
Neuropharmacology. 2019 Sep 1;155:65-75. doi: 10.1016/j.neuropharm.2019.05.016. Epub 2019 May 18.
Atomoxetine is a norepinephrine reuptake inhibitor and FDA-approved treatment for attention deficit/hyperactivity disorder (ADHD) in children, adolescents, and adults. While there is some evidence that atomoxetine may improve additional domains of cognition beyond attention in both young adults and aged individuals, this subject has not been extensively investigated. Here, we evaluated atomoxetine (in low mg/kg doses) in a variable stimulus duration (vSD) and a variable intertrial interval (vITI) version of the five choice-serial reaction time task (5C-SRTT), and an eight-arm radial arm maze (RAM) procedure in young-adult rats. The compound was further evaluated (in μg/kg-low mg/kg doses) along with nicotine (as a reference compound) and the Alzheimer's disease treatment donepezil in a distractor version of a delayed match to sample task (DMTS-D) in aged monkeys (mean age = 21.8 years). Atomoxetine (depending on the dose) improved accuracy (sustained attention) as well as behaviors related to impulsivity, compulsivity and cognitive inflexibility in both the vSD and vITI tasks and it improved spatial reference memory in the RAM. In the DMTS-D task, both nicotine and atomoxetine, but not donepezil attenuated the effects of the distractor on accuracy at short delays (non-spatial working/short term memory). However, combining sub-effective doses of atomoxetine and donepezil did enhance DMTS-D accuracy indicating the potential of using atomoxetine as an adjunctive treatment with donepezil. Collectively, these animal studies support the further evaluation of atomoxetine as a repurposed drug for younger adults as well older individuals who suffer from deficits in attention, memory and other components of executive function.
托莫西汀是一种去甲肾上腺素再摄取抑制剂,也是美国食品药品监督管理局批准的儿童、青少年和成人注意力缺陷/多动障碍(ADHD)的治疗药物。虽然有一些证据表明托莫西汀可能会改善年轻成年人和老年个体认知的其他领域,而不仅仅是注意力,但这个课题尚未得到广泛研究。在这里,我们在可变刺激持续时间(vSD)和可变试验间间隔(vITI)的五选择连续反应时任务(5C-SRTT)中评估了托莫西汀(低剂量),以及在年轻成年大鼠中进行了八臂放射臂迷宫(RAM)程序。该化合物进一步与尼古丁(作为参考化合物)和阿尔茨海默病治疗药物多奈哌齐(donepezil)一起在猴子(平均年龄为 21.8 岁)的延迟匹配样本任务(DMTS-D)的干扰版本中进行了评估(μg/kg-低剂量)。托莫西汀(取决于剂量)改善了 vSD 和 vITI 任务中的准确性(持续性注意力)以及与冲动、强迫和认知灵活性相关的行为,并且改善了 RAM 中的空间参考记忆。在 DMTS-D 任务中,尼古丁和托莫西汀(但不是多奈哌齐)都能减轻短期延迟(非空间工作/短期记忆)干扰对准确性的影响。然而,将托莫西汀和多奈哌齐的亚有效剂量结合使用可以提高 DMTS-D 的准确性,表明使用托莫西汀作为多奈哌齐的辅助治疗的潜力。总之,这些动物研究支持进一步评估托莫西汀作为一种重新定位的药物,用于治疗注意力、记忆和执行功能其他成分缺陷的年轻成年人以及老年人。