Sukhotina Irina A, Dravolina Olga A, Novitskaya Yulia, Zvartau Edwin E, Danysz Wojciech, Bespalov Anton Y
Laboratory of Behavioral Pharmacology, Institute of Pharmacology, Pavlov Medical University, 6/8 Leo Tolstoy Str., St. Petersburg, 197089, Russia.
Psychopharmacology (Berl). 2008 Feb;196(2):211-20. doi: 10.1007/s00213-007-0953-2. Epub 2007 Oct 2.
Metabotropic glutamate 1 (mGlu1) receptor antagonists were reported to induce cognitive deficits in several animal models using aversive learning procedures.
The present study aimed to further characterize behavioral effects of mGlu1 receptor antagonists using appetitively motivated tasks that evaluate working memory, timing, and impulsivity functions.
Separate groups of adult male Wistar rats were trained to perform four food-reinforced operant tasks: delayed non-matching to position (DNMTP), differential reinforcement of low rates of responding 18 s (DRL 18-s), signal duration discrimination (2-s vs 8-s bisection), and tolerance to delay of reward. Before the tests, rats were pretreated with (3-ethyl-2-methyl-quinolin-6-yl)-(4-methoxy-cyclohexyl)-methanone methanesulfonate (EMQMCM; 2.5-10 mg/kg, i.p.; JNJ16567083).
In DNMTP task, EMQMCM produced delay-dependent increases in performance accuracy so that, at 10 mg/kg dose level, percentage of correct lever choices was enhanced at 8- and 16-s delays. In DRL task, at all three tested doses, response rates were higher, and reinforcement rates were lower than under control conditions. In signal duration discrimination tasks, EMQMCM did not have any specific effects on temporal control. In tolerance to delay of reward, EMQMCM (5 and 10 mg/kg) facilitated choice of the lever associated with large reward at longer delay levels.
Blockade of mGlu1 receptors improves working memory and reduces impulsive choice at the doses that have no effects on time perception but appear to facilitate impulsive action.
据报道,在几种使用厌恶学习程序的动物模型中,代谢型谷氨酸1(mGlu1)受体拮抗剂会诱发认知缺陷。
本研究旨在使用评估工作记忆、时间安排和冲动性功能的奖励性动机任务,进一步表征mGlu1受体拮抗剂的行为效应。
将成年雄性Wistar大鼠分成不同组,训练它们执行四项食物强化操作性任务:延迟位置不匹配(DNMTP)、18秒低反应率差异强化(DRL 18-s)、信号持续时间辨别(2秒与8秒二分法)以及奖励延迟耐受性。在测试前,大鼠接受(3-乙基-2-甲基喹啉-6-基)-(4-甲氧基环己基)-甲酮甲磺酸盐(EMQMCM;2.5 - 10毫克/千克,腹腔注射;JNJ16567083)预处理。
在DNMTP任务中,EMQMCM使行为表现准确性产生延迟依赖性增加,因此在10毫克/千克剂量水平时,8秒和16秒延迟时正确杠杆选择的百分比提高。在DRL任务中,在所有三个测试剂量下,反应率均高于对照条件,强化率则低于对照条件。在信号持续时间辨别任务中,EMQMCM对时间控制没有任何特定影响。在奖励延迟耐受性方面,EMQMCM(5和10毫克/千克)在较长延迟水平下促进了与大奖励相关的杠杆选择。
在对时间感知无影响但似乎促进冲动行为的剂量下,阻断mGlu1受体会改善工作记忆并减少冲动选择。