Department of Experimental Psychology, University of Cambridge, Downing St., Cambridge, CB2 3EB, UK.
Psychopharmacology (Berl). 2011 Mar;214(2):537-48. doi: 10.1007/s00213-010-2050-1. Epub 2010 Nov 18.
Performance on the Cambridge Neuropsychological Test Automated Battery touchscreen paired-associates learning (PAL) test is predictive of Alzheimer's disease and impaired in schizophrenia and chronic drug users. An automated computer touchscreen PAL task for rats has been previously established. A pharmacologically validated PAL task for mice would be a highly valuable tool, which could be useful for a number of experimental aims including drug discovery.
This study sought to investigate the effects of systemic administration of cholinergic agents on task performance in C57Bl/6 mice.
Scopolamine hydrobromide (0.02, 0.2, and 2.0 mg/kg), dicyclomine hydrochloride (M(1) receptor antagonist; 2.0, 4.0, and 8.0 mg/kg), and donepezil hydrochloride (cholinesterase inhibitor; 0.03, 0.1, and 0.3 mg/kg) were administered post-acquisition in C57Bl/6 mice performing the PAL task.
Scopolamine (0.2 and 2.0 mg/kg) and dicyclomine (at all administered doses) significantly impaired PAL performance. A significant facilitation in PAL was revealed in mice following donepezil administration (0.3 mg/kg).
The present study shows that mice can acquire the rodent PAL task and that the cholinergic system is important for PAL task performance. M(1) receptors in particular are likely implicated in normal performance of PAL. The finding that mouse PAL can detect both impairments and improvements indicates that this task could prove to be a highly valuable tool for a number of experimental aims including drug discovery.
在剑桥神经心理学测试自动化电池触摸屏配对联想学习 (PAL) 测试中的表现可预测阿尔茨海默病,并在精神分裂症和慢性药物使用者中受损。先前已经建立了用于大鼠的自动化计算机触摸屏 PAL 任务。用于小鼠的药理学验证的 PAL 任务将是一个非常有价值的工具,它可用于许多实验目的,包括药物发现。
本研究旨在探讨系统给予胆碱能药物对 C57Bl/6 小鼠任务表现的影响。
氢溴酸东莨菪碱 (0.02、0.2 和 2.0mg/kg)、盐酸双环胺(M1 受体拮抗剂;2.0、4.0 和 8.0mg/kg)和盐酸多奈哌齐(胆碱酯酶抑制剂;0.03、0.1 和 0.3mg/kg)在 C57Bl/6 小鼠执行 PAL 任务后进行给药。
东莨菪碱(0.2 和 2.0mg/kg)和双环胺(所有给予的剂量)显著损害 PAL 表现。多奈哌齐给药后(0.3mg/kg),PAL 显著改善。
本研究表明,小鼠可以获得啮齿动物 PAL 任务,并且胆碱能系统对 PAL 任务表现很重要。特别是 M1 受体可能参与 PAL 的正常表现。发现小鼠 PAL 可以检测到损伤和改善,表明该任务可能成为许多实验目的的一个非常有价值的工具,包括药物发现。