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蝇蕈醇依赖状态的记忆:背侧海马μ-阿片受体的参与

Muscimol state-dependent memory: involvement of dorsal hippocampal mu-opioid receptors.

作者信息

Jafari-Sabet Majid, Jannat-Dastjerdi Iman

机构信息

Department of Pharmacology, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.

出版信息

Behav Brain Res. 2009 Aug 24;202(1):5-10. doi: 10.1016/j.bbr.2009.03.010. Epub 2009 Mar 19.

DOI:10.1016/j.bbr.2009.03.010
PMID:19447274
Abstract

In the present study, the effects of subcutaneous (s.c.) injections of morphine, a mu-opioid receptor agonist and intra-dorsal hippocampal (intra-CA1) injections of naloxone, a mu-opioid receptor antagonist on muscimol state-dependent memory were examined in mice. A single-trial step-down passive avoidance task was used for the assessment of memory retention in adult male NMRI mice. Pre-training intra-CA1 administration of a GABAA receptor agonist, muscimol (0.025, 0.05, 0.1 and 0.2 microg/mouse) dose dependently induced impairment of memory retention. Pre-test injection of muscimol (0.05, 0.1 and 0.2 microg/mouse, intra-CA1) induced state-dependent retrieval of the memory acquired under pre-training muscimol (0.1 microg/mouse, intra-CA1) influence. Pre-test injection of morphine (0.5 and 1 mg/kg, s.c.) 30 min before the administration of muscimol (0.1 microg/mouse, intra-CA1) dose dependently inhibited muscimol state-dependent memory. Pre-test intra-CA1 injection of naloxone (0.1 and 0.2 microg/mouse, intra-CA1) improved pre-training muscimol (0.1 microg/mouse)-induced retrieval impairment. Moreover, pre-test administration of naloxone (0.1 and 0.2 microg/mouse, intra-CA1) with an ineffective dose of muscimol (0.025 microg/mouse) significantly restored the retrieval and induced muscimol state-dependent memory. These findings implicate the involvement of a dorsal hippocampal mu-opioid receptor mechanism in muscimol state-dependent memory.

摘要

在本研究中,检测了皮下注射吗啡(一种μ-阿片受体激动剂)和海马背侧内注射纳洛酮(一种μ-阿片受体拮抗剂)对小鼠中γ-氨基丁酸A(GABAA)受体激动剂蝇蕈醇状态依赖记忆的影响。采用单次递减被动回避任务评估成年雄性NMRI小鼠的记忆保持情况。训练前在海马CA1区注射GABAA受体激动剂蝇蕈醇(0.025、0.05、0.1和0.2微克/只小鼠)剂量依赖性地诱导记忆保持受损。测试前注射蝇蕈醇(0.05、0.1和0.2微克/只小鼠,海马CA1区注射)诱导了在训练前蝇蕈醇(0.1微克/只小鼠,海马CA1区注射)影响下获得的记忆的状态依赖性提取。在注射蝇蕈醇(0.1微克/只小鼠,海马CA1区注射)前30分钟测试前注射吗啡(0.5和1毫克/千克,皮下注射)剂量依赖性地抑制了蝇蕈醇状态依赖记忆。测试前在海马CA1区注射纳洛酮(0.1和0.2微克/只小鼠,海马CA1区注射)改善了训练前蝇蕈醇(0.1微克/只小鼠)诱导的提取损伤。此外,测试前给予纳洛酮(0.1和0.2微克/只小鼠,海马CA1区注射)与无效剂量的蝇蕈醇(0.025微克/只小鼠)显著恢复了提取并诱导了蝇蕈醇状态依赖记忆。这些发现表明海马背侧μ-阿片受体机制参与了蝇蕈醇状态依赖记忆。

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