Nicotine modulates the neurotoxic effect of beta-amyloid protein((25-35)) in hippocampal cultures

被引:72
|
作者
Zamani, MR [1 ]
Allen, YS [1 ]
Owen, GP [1 ]
Gray, JA [1 ]
机构
[1] INST PSYCHIAT,DEPT PSYCHOL,LONDON SE5 8AF,ENGLAND
基金
英国惠康基金;
关键词
beta AP((25-35)); mecamylamine; neuroprotection; neurotoxicity; nicotine; rat hippocampus;
D O I
10.1097/00001756-199701200-00027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
TWO major features of Alzheimer's disease (AD) are beta-amyloid protein (beta AP) deposition and a severe cholinergic deficit. An association between the two is suggested by the negative correlation found between cigarette smoking and AD. We sought to investigate this further by examining the effects of acute and chronic nicotine exposure on beta AP-induced neuronal loss in rat hippocampal cultures. Nicotine was found to attenuate the neurotoxicity of higher concentrations of beta AP((25-35)), an effect which was enhanced by longer nicotine pretreatment and significantly inhibited by the nicotine receptor antagonist mecamylamine. Our results suggest that nicotine partially protects against the neurotoxic actions of beta AP((25-35)) via a receptor-mediated pathway.
引用
收藏
页码:513 / 517
页数:5
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