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咯利普兰通过不同的作用机制逆转东莨菪碱诱导的和时间依赖性的物体识别记忆缺陷。

Rolipram reverses scopolamine-induced and time-dependent memory deficits in object recognition by different mechanisms of action.

作者信息

Rutten K, Prickaerts J, Blokland A

机构信息

Department of Psychiatry and Neuropsychology, Brain and Behaviour Institute, Maastricht University, PO Box 616, 6200 MD Maastricht, The Netherlands.

出版信息

Neurobiol Learn Mem. 2006 Mar;85(2):132-8. doi: 10.1016/j.nlm.2005.09.002. Epub 2005 Oct 20.

Abstract

In this study, the effect of the selective phosphodiesterase type 4 (PDE4) inhibitor rolipram on memory performance was investigated using the object recognition task. First, three doses of rolipram (0.01, 0.03 or 0.1 mg/kg) were tested with a 24h delay between the learning (T1) and the test (T2) trial. Doses of rolipram were injected at different time points (30 min before T1, immediately after T1 or 3 h after T1). In a second experiment, the effects of rolipram (0.03, 0.1 or 0.3 mg/kg) were tested in combination with scopolamine (0.1 mg/kg) applying a 1 h delay between trials. Both substances were administered 30 min before T1. Using a 24h interval, rolipram showed an improvement in long-term memory performance when injected 3 h after T1 at a dose of 0.03 mg/kg. Further, rolipram reversed the scopolamine-induced short-term memory deficit at a dose of 0.1 mg/kg. Although the improved memory performance in both conditions is likely to be explained by elevated cAMP levels, two separate working mechanisms might explain these effects.

摘要

在本研究中,使用物体识别任务研究了选择性磷酸二酯酶4型(PDE4)抑制剂咯利普兰对记忆表现的影响。首先,测试了三种剂量的咯利普兰(0.01、0.03或0.1mg/kg),学习(T1)和测试(T2)试验之间间隔24小时。咯利普兰在不同时间点注射(T1前30分钟、T1后立即或T1后3小时)。在第二个实验中,测试了咯利普兰(0.03、0.1或0.3mg/kg)与东莨菪碱(0.1mg/kg)联合使用的效果,试验之间间隔1小时。两种物质均在T1前30分钟给药。间隔24小时,当在T1后3小时以0.03mg/kg的剂量注射时,咯利普兰显示出长期记忆表现有所改善。此外,咯利普兰以0.1mg/kg的剂量逆转了东莨菪碱诱导的短期记忆缺陷。尽管在两种情况下记忆表现的改善可能是由环磷酸腺苷(cAMP)水平升高所解释,但可能有两种不同的作用机制来解释这些效应。

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