Dong Xiao-xia, Wang Yan, Qin Zheng-hong
Department of Pharmacology and Laboratory of Aging and Nervous Diseases, Soochow University School of Medicine, Suzhou, China.
Acta Pharmacol Sin. 2009 Apr;30(4):379-87. doi: 10.1038/aps.2009.24.
A pivotal role for excitotoxicity in neurodegenerative diseases is gaining increasingly more acceptance, but the underlying mechanisms through which it participates in neurodegeneration still need further investigation. Excessive activation of glutamate receptors by excitatory amino acids leads to a number of deleterious consequences, including impairment of calcium buffering, generation of free radicals, activation of the mitochondrial permeability transition and secondary excitotoxicity. Recent studies implicate excitotoxicity in a variety of neuropathological conditions, suggesting that neurodegenerative diseases with distinct genetic etiologies may share excitotoxicity as a common pathogenic pathway. Thus, understanding the pathways involved in excitotoxicity is of critical importance for the future clinical treatment of many neurodegenerative diseases. This review discusses the current understanding of excitotoxic mechanisms and how they are involved in the pathogenesis of neurodegenerative diseases.
兴奋性毒性在神经退行性疾病中所起的关键作用越来越受到认可,但它参与神经退行性变的潜在机制仍需进一步研究。兴奋性氨基酸对谷氨酸受体的过度激活会导致一系列有害后果,包括钙缓冲功能受损、自由基生成、线粒体通透性转换的激活以及继发性兴奋性毒性。最近的研究表明兴奋性毒性存在于多种神经病理状况中,这表明具有不同遗传病因的神经退行性疾病可能将兴奋性毒性作为共同的致病途径。因此,了解兴奋性毒性所涉及的途径对于未来许多神经退行性疾病的临床治疗至关重要。本综述讨论了目前对兴奋性毒性机制的理解以及它们如何参与神经退行性疾病的发病过程。