首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Nphe1-Nociceptin (1-13)-NH2 a nociceptin receptor antagonist reverses nociceptin-induced spatial memory impairments in the Morris water maze task in rats
【2h】

Nphe1-Nociceptin (1-13)-NH2 a nociceptin receptor antagonist reverses nociceptin-induced spatial memory impairments in the Morris water maze task in rats

机译:Nphe1 -Nociceptin(1-13)-NH2是一种伤害感受器受体拮抗剂可逆转伤害感受器引起的大鼠莫里斯水迷宫任务中的空间记忆障碍

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

class="enumerated" style="list-style-type:decimal">The present study was undertaken to investigate the effects of the novel nociceptin receptor antagonist, [Nphe1]-Nociceptin (1-13)-NH2 (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.Nociceptin significantly impaired the ability of the animal to locate the hidden platform throughout training (P<0.001 versus control group).Pretreatment with [Nphe1]-Nociceptin (1-13)-NH2 significantly blocked nociceptin-induced impairment of spatial learning (P<0.001 versus nociceptin group).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.Learning impairments were not attributable to non-specific deficits in motor performance or change in exploratory behaviour.Taken together, our results reveal that [Nphe1]-Nociceptin (1-13)-NH2 represents an effective and useful in vivo antagonist at the nociceptin receptors involved in learning and memory.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 本研究旨在研究新型Nociceptin受体拮抗剂[Nphe 1 ]-Nociceptin(1-13)-NH2(双侧海马腔内注射,50μmol摩尔大鼠 -1 < / sup>)据称是伤害性感受态诱导的大鼠(海马双侧注射,5μmol鼠 -1 )在Morris水迷宫任务中的空间学习缺陷。此外,在“开放领域”中进行了实验,以调查可能的肽诱导的探索行为的变化。 Nociceptin显着削弱了动物在整个训练过程中定位隐藏平台的能力(P <0.001与对照组。 [Nphe 1 ]-Nociceptin(1-13)-NH2预处理可显着抑制伤害感受肽诱导的空间学习障碍(与伤害感受肽组相比,P <0.001) 一项探针试验表明,接受媒介物治疗的动物在以前包含隐藏平台的象限中花费了更多时间,而接受伤害感受素治疗的动物在任何一个象限中都没有花费更多的时间。 学习障碍并非归因于运动表现的非特定性缺陷或探索性行为的改变。 我们的研究结果表明,[Nphe 1 ]-Nociceptin( 1-13)-NH2代表与李尔有关的Nociceptin受体的有效体内拮抗剂和记忆。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号