Neuroprotective effects of extracellular glutamate are absent in hippocampal organotypic cultures treated with the amyloid peptide Aβ25-35

被引:12
|
作者
Baskys, A
Adamchik, Y
机构
[1] Univ Toronto, Dept Physiol, Toronto, ON M5T 2S8, Canada
[2] Univ Calif Irvine, Dept Psychiat & Human Behav, Orange, CA 92668 USA
[3] Long Beach VA Med Ctr, Long Beach, CA 90822 USA
关键词
amyloid peptide; glutamate; wortmannin; hippocampus; toxicity; cell death;
D O I
10.1016/S0006-8993(01)02517-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Hippocampal cells are particularly vulnerable in Alzheimer's disease but the cause of cell death is unknown. Amyloid toxicity has been implicated in hippocampal cell death, but its specific mechanisms are poorly understood. We used confocal microscopy to examine the effects of the amyloid peptide fragment 25-35 (A beta (25-35)) on cell death in organotypic hippocampal slice cultures. Addition of glutamate to the culture medium significantly improved nerve cell survival in cultures subjected to consecutive medium exchanges. This effect was lost if cultures were treated with the amyloid peptide fragment A beta (25-35) but not the inactive peptide 35-25. These data suggest that one of the mechanisms responsible for amyloid toxicity may be inhibition of the survival promoting effects of extracellular glutamate. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:188 / 194
页数:7
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