谷氨酸受体
兴奋毒性
神经科学
生物
神经传递
运输机
肌萎缩侧索硬化
兴奋性突触后电位
神经系统
谷氨酸-天冬氨酸转运体
细胞外
神经退行性变
兴奋性氨基酸转运体
细胞生物学
生物化学
医学
疾病
内科学
抑制性突触后电位
受体
基因
作者
Karen Sims,Michael B. Robinson
出处
期刊:Critical Reviews in Neurobiology
[Begell House Inc.]
日期:1999-01-01
卷期号:13 (2): 169-197
被引量:162
标识
DOI:10.1615/critrevneurobiol.v13.i2.30
摘要
Glutamate and aspartate are the primary excitatory neurotransmitters in the mammalian central nervous system and have also been implicated as mediators of excitotoxic neuronal injury and death. The precise control of extracellular glutamate and aspartate is crucial to the maintenance of normal synaptic transmission and the prevention of excitotoxicity following acute insults to the brain, such as stroke or head trauma, or during the progression of neurodegenerative diseases such as amyotrophic lateral sclerosis. The removal of excitatory amino acids (EAAs) from the extracellular space is primarily mediated by a family of sodium-dependent glutamate transporters. These transporters use the sodium electrochemical gradients of the cell to actively concentrate EAAs in both neurons and glia. Five members of this transporter family have been cloned recently and include both 'glial'-specific and 'neuron'-specific subtypes. Although these subtypes share many common functional properties, there are considerable differences in developmental expression, chronic and acute regulation by cellular signaling pathways, and contribution to disease processes among the subtypes. In this review recent studies of glutamate transporter expression, regulation, function, and pathological relevance are summarized, and some of the discrepancies and unexpected results common to any rapidly progressing field are discussed.
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