MRC Neurochemical Pathology Unit, Newcastle General Hospital, Westgate Road, Newcastle-upon-Tyne NE4 6BE, UK.
J Psychopharmacol. 1990 Jan;4(4):210-8. doi: 10.1177/026988119000400405.
Groups of rats were trained on one of two variants of an operant memory task which allows strength of memory (accuracy), bias and response rates to be measured directly. In matching to position (MTP), one of two retractable response levers appeared at random as the sample. A response caused the lever to retract and this was followed by a delay (0-64 s) interval, during which the rat had to approach, and respond at, the magazine tray. Both levers were then presented and the rat had to respond to the lever which had most recently appeared as the sample, for food reward. A second group of rats learned non-matching to position (NMTP). In this task, rats had to respond to the lever which had not appeared as the sample.The subjects were then divided into subgroups and injected, peripherally and prior to test, with one of three cholinergic drugs. These were nicotine (NIC: 0-0.3 mg/kg), oxotremorine (OXO: 0-0.3 mg/kg) and 9-amino 1,2,3,4-tetrahydroacridine (tacrine, THA: 0-3.0 mg/kg). NIC had a delay-independent disruptive effect on accuracy, but only in the non-matching version, and it did not affect rate of responding. OXO and THA had no effect on accuracy, but adversely affected response latencies and rates.The results suggest that these drugs do not affect memory mechanisms; instead, and at the doses used, certain types of bias may be induced (NIC) and general responsiveness altered (OXO and THA).
大鼠被分为几组,分别在两种操作性记忆任务变体上进行训练,这两种变体可以直接测量记忆强度(准确性)、偏差和反应率。在位置匹配(MTP)任务中,两个可伸缩反应杆中的一个随机出现在样本位置。做出反应会使杠杆缩回,然后是一个延迟(0-64 秒)间隔,在此期间大鼠必须接近并在杂志托盘上对杠杆做出反应。然后呈现两个杠杆,大鼠必须对最近作为样本出现的那个杠杆做出反应,以获得食物奖励。第二组大鼠学习非位置匹配(NMTP)任务。在这个任务中,大鼠必须对未作为样本出现的那个杠杆做出反应。然后,将这些动物分为亚组,并在测试前通过外周途径注射三种胆碱能药物中的一种。这三种药物分别是尼古丁(NIC:0-0.3mg/kg)、氧托米林(OXO:0-0.3mg/kg)和 9-氨基-1,2,3,4-四氢吖啶(tacrine,THA:0-3.0mg/kg)。NIC 对准确性有延迟无关的破坏作用,但仅在非匹配版本中,且不影响反应率。OXO 和 THA 对准确性没有影响,但会不利地影响反应潜伏期和反应率。这些结果表明,这些药物不影响记忆机制;相反,在使用的剂量下,可能会诱导某些类型的偏差(NIC)并改变一般反应性(OXO 和 THA)。