Ludolph A C, Meyer T, Riepe M W, Vökel H
Department of Neurology, University of Ulm, D-89075 Ulm, Steinhövelstrasse 9, Germany.
Restor Neurol Neurosci. 1998;13(1-2):59-67.
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.
肌萎缩侧索硬化症是一种进行性致命疾病,会破坏人类的脊髓和大脑。有研究表明,兴奋性毒性参与了肌萎缩侧索硬化症的发病机制。这一假说推动了大量基础研究,并促进了针对慢性神经退行性疾病的神经保护疗法的发展。经过这些努力,一种抗谷氨酸能药物利鲁唑已被确立用于治疗肌萎缩侧索硬化症。随后培育出了一种具有肌萎缩侧索硬化症特征的转基因小鼠,以便在体内对该疾病进行研究。然而,尽管取得了相当大的进展,但肌萎缩侧索硬化症的病因仍然不明,兴奋性神经传递的紊乱绝不应被视为该疾病发病机制所特有的。