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[苯丙氨酸(1)]-孤啡肽(1 - 13)-NH₂,一种孤啡肽受体拮抗剂,可逆转大鼠在莫里斯水迷宫任务中孤啡肽诱导的空间记忆损伤。

[Nphe(1)]-Nociceptin (1-13)-NH(2), a nociceptin receptor antagonist, reverses nociceptin-induced spatial memory impairments in the Morris water maze task in rats.

作者信息

Redrobe J P, Calo G, Guerrini R, Regoli D, Quirion R

机构信息

Douglas Hospital Research Centre, Department of Psychiatry, McGill University, 6875 Blvd LaSalle, Verdun, QC, Canada, H4H 1R3.

出版信息

Br J Pharmacol. 2000 Dec;131(7):1379-84. doi: 10.1038/sj.bjp.0703724.

Abstract
  1. The present study was undertaken to investigate the effects of the novel nociceptin receptor antagonist, [Nphe(1)]-Nociceptin (1-13)-NH(2) (bilateral intrahippocampal injection, 50 nmole rat(-1)) on purported nociceptin-induced (bilateral intrahippocampal injection, 5 nmole rat(-1)) deficits in spatial learning in the rat Morris water maze task. In addition, experiments were performed in an 'open field' to investigate possible peptide-induced changes in exploratory behaviour. 2. Nociceptin significantly impaired the ability of the animal to locate the hidden platform throughout training (P<0.001 versus control group). 3. Pretreatment with [Nphe(1)]-Nociceptin (1-13)-NH(2) significantly blocked nociceptin-induced impairment of spatial learning (P<0.001 versus nociceptin group). 4. A probe trial revealed that vehicle-treated animals spent more time in the quadrant that had previously contained the hidden platform, whereas nociceptin-treated animals did not spend more time in any one quadrant. 5. Learning impairments were not attributable to non-specific deficits in motor performance or change in exploratory behaviour. 6. Taken together, our results reveal that [Nphe(1)]-Nociceptin (1-13)-NH(2) represents an effective and useful in vivo antagonist at the nociceptin receptors involved in learning and memory.
摘要
  1. 本研究旨在探讨新型孤啡肽受体拮抗剂[Nphe(1)]-孤啡肽(1 - 13)-NH₂(双侧海马内注射,50纳摩尔/大鼠)对孤啡肽诱导(双侧海马内注射,5纳摩尔/大鼠)的大鼠莫里斯水迷宫任务空间学习缺陷的影响。此外,在“旷场”中进行实验,以研究肽诱导的探索行为可能发生的变化。2. 孤啡肽在整个训练过程中显著损害动物定位隐藏平台的能力(与对照组相比,P<0.001)。3. 用[Nphe(1)]-孤啡肽(1 - 13)-NH₂预处理可显著阻断孤啡肽诱导的空间学习损伤(与孤啡肽组相比,P<0.001)。4. 一次探索性试验显示,注射溶剂的动物在先前放置隐藏平台的象限花费更多时间,而注射孤啡肽的动物在任何一个象限都没有花费更多时间。5. 学习障碍并非归因于运动表现的非特异性缺陷或探索行为的改变。6. 综上所述,我们的结果表明,[Nphe(1)]-孤啡肽(1 - 13)-NH₂是参与学习和记忆的孤啡肽受体的一种有效的体内拮抗剂。

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