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大鼠和猴子中的东莨菪碱逆转范式:计算机辅助操作性条件记忆任务在筛选候选药物中的重要性。

The scopolamine-reversal paradigm in rats and monkeys: the importance of computer-assisted operant-conditioning memory tasks for screening drug candidates.

作者信息

Buccafusco Jerry J, Terry Alvin V, Webster Scott J, Martin Daniel, Hohnadel Elizabeth J, Bouchard Kristy A, Warner Samantha E

机构信息

Alzheimer's Research Center, Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA 30912, USA.

出版信息

Psychopharmacology (Berl). 2008 Aug;199(3):481-94. doi: 10.1007/s00213-007-0887-8. Epub 2007 Jul 27.

Abstract

RATIONALE

The scopolamine-reversal model is enjoying a resurgence of interest in clinical studies as a reversible pharmacological model for Alzheimer's disease (AD). The cognitive impairment associated with scopolamine is similar to that in AD. The scopolamine model is not simply a cholinergic model, as it can be reversed by drugs that are noncholinergic cognition-enhancing agents.

OBJECTIVES

The objective of the study was to determine relevance of computer-assisted operant-conditioning tasks in the scopolamine-reversal model in rats and monkeys.

MATERIALS AND METHODS

Rats were evaluated for their acquisition of a spatial reference memory task in the Morris water maze. A separate cohort was proficient in performance of an automated delayed stimulus discrimination task (DSDT). Rhesus monkeys were proficient in the performance of an automated delayed matching-to-sample task (DMTS).

RESULTS

The AD drug donepezil was evaluated for its ability to reverse the decrements in accuracy induced by scopolamine administration in all three tasks. In the DSDT and DMTS tasks, the effects of donepezil were delay (retention interval)-dependent, affecting primarily short delay trials. Donepezil produced significant but partial reversals of the scopolamine-induced impairment in task accuracies after 2 mg/kg in the water maze, after 1 mg/kg in the DSDT, and after 50 microg/kg in the DMTS task.

CONCLUSIONS

The two operant-conditioning tasks (DSDT and DMTS) provided data most in keeping with those reported in clinical studies with these drugs. The model applied to nonhuman primates provides an excellent transitional model for new cognition-enhancing drugs before clinical trials.

摘要

原理

东莨菪碱逆转模型作为阿尔茨海默病(AD)的一种可逆药理学模型,在临床研究中重新受到关注。与东莨菪碱相关的认知障碍与AD中的相似。东莨菪碱模型并非简单的胆碱能模型,因为它可被非胆碱能认知增强剂药物逆转。

目的

本研究的目的是确定计算机辅助操作性条件任务在大鼠和猴子东莨菪碱逆转模型中的相关性。

材料与方法

评估大鼠在莫里斯水迷宫中获取空间参考记忆任务的能力。另一组大鼠熟练掌握自动延迟刺激辨别任务(DSDT)。恒河猴熟练掌握自动延迟匹配样本任务(DMTS)。

结果

评估了AD药物多奈哌齐在所有三项任务中逆转东莨菪碱给药引起的准确性下降的能力。在DSDT和DMTS任务中,多奈哌齐的作用取决于延迟(保留间隔),主要影响短延迟试验。在水迷宫中给予2mg/kg、在DSDT中给予1mg/kg、在DMTS任务中给予50μg/kg后,多奈哌齐显著但部分逆转了东莨菪碱引起的任务准确性损害。

结论

两项操作性条件任务(DSDT和DMTS)提供的数据与这些药物临床研究中报告的数据最为一致。应用于非人灵长类动物的模型为新的认知增强药物在临床试验前提供了一个极好的过渡模型。

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