Cole B J, Hillmann M
Department of Neuropsychopharmacology, Research Laboratories of Schering AG, Berlin, Germany.
Psychopharmacology (Berl). 1994 Jul;115(3):350-7. doi: 10.1007/BF02245076.
The effects of a series of benzodiazepine (BZ) receptor ligands, ranging from a full agonist through to partial inverse agonists, were examined on short term working memory in the rat. The behavioural paradigm used was a discrete trial, operant delayed matching to position task, as originally described by Dunnett (1985), with delays of 0, 5, 15 and 30 s. The benzodiazepine receptor (BZR) full agonist lorazepam (0.25, 0.375 and 0.5 mg/kg) dose and delay dependently impaired matching accuracy. Lorazepam also increased the latency to respond and decreased the number of nose pokes made into the food tray during the delays. In contrast, the BZR partial agonist ZK 95,962 (1, 3, 10 mg/kg) did not affect matching accuracy, but did increase the speed of responding. The BZR antagonist ZK 93,426 (1.25, 5, 25 mg/kg) had no effects in this paradigm. The BZR weak partial inverse agonists Ro 15-4513 (0.1, 1 and 10 mg/kg) and ZK 90,886 (1, 3 and 10 mg/kg) did not affect accuracy of performance. However, both of these drugs increased the latency to respond and decreased nose poke responses. These motoric effects were particularly strong following 10 mg/kg Ro 15-4513. This shows that the effects of drugs on the accuracy of responding and on the speed of responding can be dissociated. The BZR partial inverse agonist FG 7142 had effects on matching accuracy that were dependent upon dose. The lowest dose of FG 7142 (1 mg/kg) significantly improved accuracy, whereas the highest dose (10 mg/kg) impaired accuracy.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了一系列苯二氮䓬(BZ)受体配体(从完全激动剂到部分反向激动剂)对大鼠短期工作记忆的影响。所采用的行为范式是一种离散试验、操作性延迟位置匹配任务,如Dunnett(1985年)最初描述的那样,延迟时间为0、5、15和30秒。苯二氮䓬受体(BZR)完全激动剂劳拉西泮(0.25、0.375和0.5毫克/千克)剂量和延迟时间依赖性地损害匹配准确性。劳拉西泮还增加了反应潜伏期,并减少了延迟期间进入食物托盘的鼻触次数。相比之下,BZR部分激动剂ZK 95,962(1、3、10毫克/千克)不影响匹配准确性,但确实提高了反应速度。BZR拮抗剂ZK 93,426(1.25、5、25毫克/千克)在此范式中没有作用。BZR弱部分反向激动剂Ro 15 - 4513(0.1、1和10毫克/千克)和ZK 90,886(1、3和10毫克/千克)不影响行为表现的准确性。然而,这两种药物都增加了反应潜伏期并减少了鼻触反应。这些运动效应在10毫克/千克Ro 15 - 4513后尤为强烈。这表明药物对反应准确性和反应速度的影响可以分开。BZR部分反向激动剂FG 7142对匹配准确性的影响取决于剂量。FG 7142的最低剂量(1毫克/千克)显著提高了准确性,而最高剂量(10毫克/千克)则损害了准确性。(摘要截短至250字)