Beyond NMDA and AMPA glutamate receptors: emerging mechanisms for ionic imbalance and cell death in stroke

被引:182
作者
Besancon, Elaine [3 ]
Guo, Shuzhen [3 ,4 ,5 ]
Lok, Josephine [3 ,6 ]
Tymianski, Michael [1 ,2 ]
Lo, Eng H. [3 ,4 ,5 ]
机构
[1] Univ Toronto, Toronto Western Res Inst, Toronto, ON M5T 2S8, Canada
[2] Univ Toronto, Dept Neurosurg, Toronto, ON M5T 2S8, Canada
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Neuroprotect Res Lab, Boston, MA 02129 USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiol, Boston, MA 02129 USA
[5] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Neurol, Boston, MA 02129 USA
[6] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Pediat, Boston, MA 02114 USA
关键词
D O I
10.1016/j.tips.2008.02.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The glutamate receptor was one of the most intensely investigated targets for neuroprotection. However, numerous clinical trials of glutamate receptor antagonists for the treatment of stroke were unsuccessful. These failures have led to pessimism in the field. But recent advances could provide hope for the future. This minireview looks beyond the traditional mechanism of glutamate-receptor-driven excitotoxicity to identify other mechanisms of ionic imbalance. These advances include findings implicating sodium-calcium exchangers, hemi-channels, volume-regulated anion channels, acid-sensing channels, transient receptor potential channels, nonselective cation channels and signaling cascades that mediate crosstalk between redundant pathways of cell death. Further in vivo validation of these pathways could ultimately lead us to new therapeutic targets for stroke, trauma and neurodegeneration.
引用
收藏
页码:268 / 275
页数:8
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