Sirviö J, Riekkinen P, Ekonsalo T, Lammintausta R, Riekkinen P J
Department of Neurology, University of Kuopio, Finland.
Neuropharmacology. 1992 Feb;31(2):163-8. doi: 10.1016/0028-3908(92)90027-m.
The effects of dexmedetomidine, a specific and potent alpha 2 agonist, on the performance of rats in passive avoidance and water maze tasks were studied. Pre-training administration of subanaesthetic dose (9.0 micrograms/kg) of dexmedetomidine impaired the retention of the passive avoidance task (assessed 24 hr after training) but it did not affect the training of this task. Smaller doses (0.3, 0.9 and 3.0 micrograms/kg) did not affect the training or retention of this aversively motivated task. On the other hand, pre-training administration of 0.3 and 0.9 microgram/kg dexmedetomidine impaired the acquisition of the water maze task, whereas larger doses (3.0 and 9.0 micrograms/kg) had no significant effect on spatial learning. Pre-training administration of dexmedetomidine (0.3-9.0 micrograms/kg) increased swimming speed in rats. Only a large dose (300 micrograms/kg) of dexmedetomidine, administered immediately after training, impaired the retention of the passive avoidance task and the acquisition of the water maze task. These data agree with previous findings that pharmacological manipulation of the noradrenergic system affects the retention of aversively-motivated (passive avoidance) tasks. The present results suggest that the dose-response curve of dexmedetomidine for impairment of learning/memory differs between the passive avoidance and water maze tasks.
研究了特异性强效α2激动剂右美托咪定对大鼠在被动回避和水迷宫任务中的表现的影响。术前给予亚麻醉剂量(9.0微克/千克)的右美托咪定损害了被动回避任务的记忆保持(训练后24小时评估),但不影响该任务的训练。较小剂量(0.3、0.9和3.0微克/千克)不影响此厌恶性动机任务的训练或记忆保持。另一方面,术前给予0.3和0.9微克/千克右美托咪定损害了水迷宫任务的习得,而较大剂量(3.0和9.0微克/千克)对空间学习无显著影响。术前给予右美托咪定(0.3 - 9.0微克/千克)可提高大鼠的游泳速度。仅在训练后立即给予大剂量(300微克/千克)右美托咪定损害了被动回避任务的记忆保持和水迷宫任务的习得。这些数据与先前的研究结果一致,即去甲肾上腺素能系统的药理学操作会影响厌恶性动机(被动回避)任务的记忆保持。目前的结果表明,右美托咪定对学习/记忆损害的剂量反应曲线在被动回避和水迷宫任务之间有所不同。