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首页> 外文期刊>Psychopharmacology >An inverse agonist selective for alpha5 subunit-containing GABAA receptors improves encoding and recall but not consolidation in the Morris water maze.
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An inverse agonist selective for alpha5 subunit-containing GABAA receptors improves encoding and recall but not consolidation in the Morris water maze.

机译:对含有alpha5亚基的GABAA受体具有选择性的反向激动剂可以改善莫里斯水迷宫中的编码和记忆,但不能增强固结。

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摘要

RATIONALE: Compounds selective for the GABAA receptors containing an alpha5 subunit have been reported to enhance performance in the hippocampally mediated delayed-matching-to-position version of the Morris water maze, in which reduction in the time required to find a hidden platform relative to an initial trial is used as an index of learning and memory. OBJECTIVE: In the present study, we have used one such compound, alpha5IA-II, to examine whether these effects occur during the encoding, consolidation or recall phases of this paradigm. METHODS: alpha5IA-II was administered in the absence or presence of the benzodiazepine site antagonist flumazenil, so as to limit its action to periods associated with encoding, consolidation and recall. Drug doses and timings of administrations were defined using occupancy data derived from an in vivo [3H]flumazenil binding assay. Similar experiments were carried out to study the memory-disruptive properties of chlordiazepoxide (CDP). RESULTS: The trial 1 to trial 2 difference was increased when alpha5IA-II was given before either trial 1 or trial 2, indicating an effect on the encoding and recall phases, respectively, of learning and memory. Conversely, alpha5IA-II had no effect on performance when given immediately after trial 1, suggesting that it had no effect on the consolidation phase. In contrast to the facilitation of performance produced by the alpha5-selective inverse agonist alpha5IA-II given during the encoding and recall but not the consolidation phase, the non-selective agonist CDP impaired performance when given during the encoding and recall phases, whilst having no effect on the consolidation phase. CONCLUSIONS: These data further highlight the cognition-enhancing properties of GABAA alpha5-selective inverse agonists and define the functional specificity of these effects in terms of encoding and recall processes in the Morris water maze.
机译:理由:据报道,对含有α5亚基的GABAA受体具有选择性的化合物可增强海马介导的莫里斯水迷宫延迟匹配位置的性能,从而减少了相对于隐藏迷宫找到隐藏平台所需的时间初步试验被用作学习和记忆的指标。目的:在本研究中,我们使用了一种这样的化合物alpha5IA-II来检查这些效应是否在此范例的编码,合并或召回阶段发生。方法:在不存在或存在苯二氮卓类拮抗剂氟马西尼的情况下施用alpha5IA-II,以将其作用限制在与编码,巩固和回忆相关的时期。使用从体内[3H]氟马西尼结合测定得出的占用数据定义药物剂量和给药时间。进行了类似的实验,以研究氯二氮卓(CDP)的破坏记忆的特性。结果:当在试验1或试验2之前使用alpha5IA-II时,试验1与试验2的差异增加,表明分别对学习和记忆的编码和回忆阶段有影响。相反,在试验1之后立即给予alpha5IA-II对性能没有影响,表明它对巩固阶段没有影响。与编码和召回阶段提供的alpha5选择性反向激动剂alpha5IA-II产生的性能促进相反,而合并阶段却没有,相反,编码和召回阶段提供的非选择性激动剂CDP损害了性能,而没有对巩固阶段的影响。结论:这些数据进一步突出了GABAAα5选择性反向激动剂的认知增强特性,并根据莫里斯水迷宫中的编码和召回过程定义了这些效应的功能特异性。

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