A LONG-ACTING CHOLINESTERASE INHIBITOR REVERSES SPATIAL MEMORY DEFICITS IN MICE

被引:71
作者
SWEENEY, JE
HOHMANN, CF
MORAN, TH
COYLE, JT
机构
[1] JOHNS HOPKINS UNIV, SCH MED,DEPT PSYCHIAT,MEYER 4-163,600 N WOLFE ST, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS UNIV, SCH PUBL HLTH, DEPT ENVIRONM HLTH SCI, DIV NEUROTOXICOL, BALTIMORE, MD 21205 USA
[3] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROSCI, BALTIMORE, MD 21205 USA
[4] JOHNS HOPKINS UNIV, SCH MED, DEPT PHARMACOL, BALTIMORE, MD 21205 USA
关键词
D O I
10.1016/0091-3057(88)90325-5
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The effects of the long-acting acetylcholinesterase (AChE) inhibitor, galanthamine, on spatial memory were investigated in mice. Mice received ibotenic acid or sham lesions to the nucleus basalis magnocellularis (nBM). Groups of nBM-lesioned and control mice were then trained on a modified Morris swim maze task. Each mouse was first placed on a platform and then into quadrants of the swim tank in a random order. Time required to find the hidden platform was measured. In different phases of testing, the animal had to find a platform that either remained in the same quadrant (reference memory component) or was moved daily (working memory component). The nBM-lesioned mice took significantly longer to find the platform as compared to controls on the working, but not on the reference, memory component of the task. Galanthamine (5.0 mg/kg, IP), given 3.5 hours before testing, improved performance on the working memory task in nBM-lesioned mice by 70% and strikingly impaired performance in controls. Galanthamine''s ability to reverse cognitive deficits induced by nBM lesions and its comparatively long half-life suggest that it may be effective in treating the central cholinergic deficits in Alzheimer''s disease patients.
引用
收藏
页码:141 / 147
页数:7
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