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κ阿片受体激动剂与μ、δ阿片受体拮抗剂对记忆提取的增强作用

Memory retrieval enhancement by kappa opioid agonist and mu, delta antagonists.

作者信息

Ilyutchenok R Y, Dubrovina N I

机构信息

Laboratory of the Memory Mechanisms, Institute of Physiology Siberian Branch of the Russian Academy of Medical Sciences, Novosibirsk, Russia.

出版信息

Pharmacol Biochem Behav. 1995 Dec;52(4):683-7. doi: 10.1016/0091-3057(95)00099-i.

Abstract

The present study sought to identify specific opioid receptor subtypes involved in the modulation of reactivation of amnesic or forgotten memory traces by use of a one-trial inhibitory avoidance training procedures in mice. The effects of naloxone, ICI 174,864 (mu and delta opioid receptor antagonists, respectively) and dynorphin (kappa agonist) were investigated. The results indicated that preretention test administration of naloxone (2 mg/kg) or ICI 174,864 (3 mg/kg) attenuated the amnesia and forgetting as indicated by prolongation of step-through latency. On the other hand, the activation of kappa opioid receptors by dynorphin (1 mg/kg) also showed reactivating effects both after amnesia and forgetting. On the basis of the parallelism of the effects for mu and delta opioid receptor antagonists and kappa agonist, and on the finding that all three opioids demonstrated a different degree of reactivation of amnesic and forgotten memory traces, it was concluded that mu, delta, and kappa opioid receptors contribute to the modulation of amnesia and forgetting by independent mechanisms.

摘要

本研究旨在通过在小鼠中使用一次性抑制性回避训练程序,确定参与调节失忆或遗忘记忆痕迹重新激活的特定阿片受体亚型。研究了纳洛酮、ICI 174,864(分别为μ和δ阿片受体拮抗剂)和强啡肽(κ激动剂)的作用。结果表明,在记忆保持前测试时给予纳洛酮(2mg/kg)或ICI 174,864(3mg/kg)可减轻失忆和遗忘,表现为穿通潜伏期延长。另一方面,强啡肽(1mg/kg)激活κ阿片受体在失忆和遗忘后也显示出重新激活作用。基于μ和δ阿片受体拮抗剂与κ激动剂作用的平行性,以及所有三种阿片类药物均表现出不同程度的失忆和遗忘记忆痕迹重新激活这一发现,得出结论:μ、δ和κ阿片受体通过独立机制参与失忆和遗忘的调节。

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