Terry Alvin V, Callahan Patrick M, Schade Rosann, Kille Nancy J, Plagenhoef Marc
Department of Pharmacology and Toxicology, Georgia Regents University, Augusta, GA 30912, United States; Small Animal Behavior Core, Georgia Regents University, Augusta, GA 30912, United States.
Department of Pharmacology and Toxicology, Georgia Regents University, Augusta, GA 30912, United States; Small Animal Behavior Core, Georgia Regents University, Augusta, GA 30912, United States.
Pharmacol Biochem Behav. 2014 Nov;126:63-72. doi: 10.1016/j.pbb.2014.09.010. Epub 2014 Sep 19.
There is considerable evidence that centrally acting α2A adrenergic receptor agonists can attenuate impairments in executive function that result from dysfunction of the prefrontal cortex. Such positive effects resulted in the recent approval by the United States Food and Drug Administration (FDA) of the α2A agonists clonidine and guanfacine for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD), but also suggest that they could have beneficial effects in substance abuse disorders and other neuropsychiatric conditions. The purpose of this study was to evaluate guanfacine for its ability to attenuate behavioral alterations associated with acute cocaine exposure in rats trained to perform a task of sustained attention, the five choice serial reaction time task (5C-SRTT) and monkeys trained to perform a task of working/short term memory, the delayed match to sample (DMTS) task. In the rodent 5C-SRTT acute intraperitoneal (i.p.) administration of cocaine (3.5-15.0mg/kg) did not affect accuracy, but was associated with dose-dependent increases in premature responses and timeout responses. Guanfacine (0.1-1.0mg/kgi.p.) dose-dependently decreased premature responses and timeout responses associated with cocaine and it attenuated similar deficits in inhibitory response control observed in a variable ITI version of the 5C-SRTT. In the DMTS task in monkeys, acute intramuscular (i.m.) administration of cocaine (4.0mg/kg) was associated with impairments in accuracy at long delay intervals, an effect that was attenuated by guanfacine (0.4mg/kg). These animal studies suggest that guanfacine may have therapeutic potential for treating impairments of executive function that are associated with the abuse of cocaine.
有大量证据表明,中枢作用的α2A肾上腺素能受体激动剂可减轻前额叶皮质功能障碍导致的执行功能损害。这种积极作用导致美国食品药品监督管理局(FDA)最近批准α2A激动剂可乐定和胍法辛用于治疗注意力缺陷多动障碍(ADHD),但也表明它们可能对物质使用障碍和其他神经精神疾病有有益作用。本研究的目的是评估胍法辛在患有持续性注意力任务(五选择连续反应时任务,5C-SRTT)的大鼠以及患有工作/短期记忆任务(延迟匹配样本,DMTS)的猴子中减轻与急性可卡因暴露相关的行为改变的能力。在啮齿动物的5C-SRTT中,急性腹腔注射(i.p.)可卡因(3.5 - 15.0mg/kg)不影响准确性,但与过早反应和超时反应的剂量依赖性增加有关。胍法辛(0.1 - 1.0mg/kg i.p.)剂量依赖性地减少了与可卡因相关的过早反应和超时反应,并减轻了在5C-SRTT的可变ITI版本中观察到的抑制反应控制方面的类似缺陷。在猴子的DMTS任务中,急性肌肉注射(i.m.)可卡因(4.0mg/kg)与长延迟间隔时的准确性受损有关,胍法辛(0.4mg/kg)可减轻这种影响。这些动物研究表明,胍法辛可能具有治疗与可卡因滥用相关的执行功能损害的治疗潜力。