Molecular and cellular mechanisms of excitotoxic neuronal death

被引:409
作者
Wang, Yan [1 ,2 ]
Qin, Zheng-hong [1 ,2 ]
机构
[1] Soochow Univ, Dept Pharmacol, Sch Med, Suzhou 215123, Peoples R China
[2] Soochow Univ, Lab Aging & Nervous Dis SZS0703, Sch Med, Suzhou 215123, Peoples R China
关键词
Excitotoxicity; Glutamate receptor; Mitochondria; Protease; Neurological disorder; METABOTROPIC GLUTAMATE RECEPTORS; EXCITATORY AMINO-ACID; NF-KAPPA-B; ENDOPLASMIC-RETICULUM STRESS; CYTOCHROME-C RELEASE; AMYOTROPHIC-LATERAL-SCLEROSIS; OXYGEN-GLUCOSE DEPRIVATION; SIGNAL-REGULATED KINASES; ACTIVATED PROTEIN-KINASE; TRANSGENIC MOUSE MODEL;
D O I
10.1007/s10495-010-0481-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Glutamate receptor-mediated excitatory neurotransmission plays a key role in neural development, differentiation and synaptic plasticity. However, excessive stimulation of glutamate receptors induces neurotoxicity, a process that has been defined as excitotoxicity. Excitotoxicity is considered to be a major mechanism of cell death in a number of central nervous system diseases including stroke, brain trauma, epilepsy and chronic neurodegenerative disorders. Unfortunately clinical trials with glutamate receptor antagonists, that would logically prevent the effects of excessive receptor activation, have been associated with untoward side effects or little clinical benefit. Therefore, uncovering molecular pathways involved in excitotoxic neuronal death is of critical importance to future development of clinical treatment of many neurodegenerative disorders where excitotoxicity has been implicated. This review discusses the current understanding of the molecular and cellular mechanisms of excitotoxicity and their roles in the pathogenesis of diseases of the central nervous system.
引用
收藏
页码:1382 / 1402
页数:21
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