Kameyama T, Nabeshima T, Kozawa T
Pharmacol Biochem Behav. 1986 Sep;25(3):567-72. doi: 10.1016/0091-3057(86)90142-5.
The amnesia induced by cycloheximide (CXM) injected SC and by CXM or anisomycin injected ICV immediately after the training test was antagonized in combination with an opiate antagonist, naloxone (NLX). This antagonism occurred on both the passive avoidance- and escape-learning responses in a dose-dependent manner in mice. NLX alone (0.3-10.0 mg/kg) did not alter the performances of these tasks. Furthermore, the decrease in retention performance on shuttle avoidance in rats induced by CXM was also antagonized by NLX. Treatment with CXM and/or NLX did not affect spontaneous locomotor activity. The interaction of these drugs on the performance of the passive avoidance- and escape-learning and the shuttle avoidance tasks may be related to neurochemical memory processes. These results suggest that an opioid system may participate in the amnesic actions induced by protein synthesis inhibitors in these models.
在训练测试后立即皮下注射环己酰亚胺(CXM)以及脑室内注射CXM或茴香霉素所诱导的失忆,在与阿片类拮抗剂纳洛酮(NLX)联合使用时受到拮抗。这种拮抗作用在小鼠的被动回避和逃避学习反应中均呈剂量依赖性发生。单独使用NLX(0.3 - 10.0毫克/千克)不会改变这些任务的表现。此外,CXM诱导的大鼠穿梭回避记忆保持能力的下降也被NLX拮抗。用CXM和/或NLX治疗不影响自发运动活动。这些药物在被动回避、逃避学习和穿梭回避任务表现上的相互作用可能与神经化学记忆过程有关。这些结果表明,在这些模型中,阿片系统可能参与了蛋白质合成抑制剂诱导的失忆作用。