肌萎缩侧索硬化
利鲁唑
兴奋毒性
神经科学
医学
神经保护
发病机制
脊髓
谷氨酸受体
疾病
病理
生物
内科学
受体
作者
Albert C. Ludolph,Thomas Meyer,M. Riepe,Helge Völkel
出处
期刊:Restorative Neurology and Neuroscience
[IOS Press]
日期:1998-01-01
卷期号:13 (1-2): 59-67
被引量:14
标识
DOI:10.3233/rnn-1998-00050
摘要
Amyotrophic lateral sclerosis is a progressive fatal disorder devastating the spinal cord and brain in humans. Excitotoxicity has been suggested to be involved in the pathogenesis of amyotrophic lateral sclerosis. This hypothesis has driven a wealth of basic research and stimulated development of neuroprotective therapies for chronic neurodegenerative disorders. As a result of these efforts, riluzole, an antiglutamatergic drug, has been established in the therapy of amyotrophic lateral sclerosis. A transgenic mouse showing features of amyotrophic lateral sclerosis has been subsequently engineered enabling studies of the disease in vivo. However, despite considerable progress, the etiology of amyotrophic lateral sclerosis remains obscure and the disturbances in excitatory neurotransmission should by no means be regarded as exclusive to the pathogenesis of the disease.
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