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一种对含α5亚基的GABAA受体具有选择性的反向激动剂可改善Morris水迷宫中的编码和记忆提取,但不影响记忆巩固。

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

作者信息

Collinson N, Atack J R, Laughton P, Dawson G R, Stephens D N

机构信息

Merck Sharp and Dohme Research Laboratories, The Neuroscience Research Centre, Terlings Park, Harlow,, Essex, CM20 2QR, UK.

出版信息

Psychopharmacology (Berl). 2006 Nov;188(4):619-28. doi: 10.1007/s00213-006-0361-z. Epub 2006 Apr 22.

Abstract

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.

摘要

理论依据

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在莫里斯水迷宫的海马介导的位置延迟匹配版本中的表现,其中相对于初始试验,找到隐藏平台所需时间的减少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α5IA-II,来研究这些效应是否发生在该范式的编码、巩固或回忆阶段。

方法

在不存在或存在苯二氮䓬位点拮抗剂氟马西尼的情况下给予α5IA-II,以便将其作用限制在与编码、巩固和回忆相关的时期。使用源自体内[3H]氟马西尼结合试验的占有率数据确定药物剂量和给药时间。进行了类似的实验以研究氯氮䓬(CDP)的记忆破坏特性。

结果

在试验1或试验2之前给予α5IA-II时,试验1到试验2的差异增加,分别表明对学习和记忆的编码和回忆阶段有影响。相反,在试验1后立即给予α5IA-II对表现没有影响,表明它对巩固阶段没有影响。与在编码和回忆阶段而非巩固阶段给予α5选择性反向激动剂α5IA-II所产生的表现促进作用相反,非选择性激动剂CDP在编码和回忆阶段给予时会损害表现,而对巩固阶段没有影响。

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回忆过程定义了这些效应的功能特异性。

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