兴奋毒性
NMDA受体
神经科学
受体
谷氨酸受体
神经保护
生物
调解人
神经退行性变
谷氨酸的
AMPA受体
医学
细胞生物学
疾病
生物化学
作者
Elisa A. Waxman,David R. Lynch
标识
DOI:10.1177/1073858404269012
摘要
N-methyl-D-aspartate (NMDA) receptors are the major mediator of excitotoxicity. Although physiological activation of the NMDA receptor is necessary for cell survival, overactivation is a signal for cell death. Several pathways are activated through NMDA receptor stimulation, most of which can contribute to excitotoxicity. These include events leading to mitochondrial dysfunction, activation of calcium-dependent enzymes, and activation of mitogen-activated protein kinase pathways. Understanding the role of these mechanisms is important in developing agents that block excitotoxicity without inhibiting functions necessary for survival. NMDA receptor subtypes may be responsible for mediating separate pathways, and subtype-specific inhibition has shown promising results in some neurological models. This review examines the roles of NMDA receptor subtypes in excitotoxicity and neurological disorders.
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