Stroke intervention pathways: NMDA receptors and beyond

被引:149
作者
Lai, Ted Weita [1 ,2 ,3 ]
Shyu, Woei-Cherng [3 ,4 ,5 ]
Wang, Yu Tian [1 ,2 ]
机构
[1] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Dept Med, Vancouver, BC V6T 2B5, Canada
[3] China Med Univ & Hosp, Translat Med Res Ctr, Taichung 40447, Taiwan
[4] China Med Univ & Hosp, Ctr Neuropsychiat, Taichung 40447, Taiwan
[5] China Med Univ & Hosp, Grad Inst Immunol, Taichung 40447, Taiwan
基金
加拿大健康研究院;
关键词
ACTIVATED PROTEIN-KINASE; ISCHEMIC BRAIN-INJURY; LONG-TERM DEPRESSION; CEREBRAL-ISCHEMIA; CELL-DEATH; SUBUNIT COMPOSITION; IN-VITRO; HIPPOCAMPAL-NEURONS; DIFFERENTIAL ROLES; PEPTIDE INHIBITOR;
D O I
10.1016/j.molmed.2010.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite abundant evidence from basic/preclinical research that excessive NMDAR (N-methyl-D-aspartate receptor) stimulation is a crucial step required for brain damage following a stroke, clinical trials for NMDAR blockers have all ended with disappointments. The past decade of stroke research has revealed distinct NMDAR subpopulations and many specific effectors downstream of these receptors that are differentially responsible for neuronal survival and death. These new advancements provide promising targets for the development of novel NMDAR-based neuroprotective stroke therapies that could have greater therapeutic windows and reduced side effects. In this review, we discuss these advancements with a particular emphasis on the identification of novel signaling effectors downstream of proneuronal death NMDARs and the potential implications of these findings for the development of stroke therapeutics.
引用
收藏
页码:266 / 275
页数:10
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