Stys Peter K, Lipton Stuart A
Department of Clinical Neurosciences, Hotchkiss Brain Institute, University of Calgary, AB, T2N 4N1, Canada.
Trends Pharmacol Sci. 2007 Nov;28(11):561-6. doi: 10.1016/j.tips.2007.10.003. Epub 2007 Oct 24.
Axons, their ensheathing myelin and supporting glia that make up the white matter in the mammalian brain and spinal cord are fundamentally important for the normal operation of the central nervous system. Prevalent human disorders such as stroke, vascular dementia, multiple sclerosis, brain and spinal cord trauma, HIV-associated dementia, periventricular leukomalacia of premature infants, and seemingly traditional 'gray matter disorders' such as Alzheimer's disease and schizophrenia, exhibit white matter pathology that contributes to morbidity and mortality. N-Methyl-D-aspartate (NMDA) receptors have been shown to have an important role in mediating Ca2+-dependent injury of oligodendrocytes and the myelin sheath; newly recognized family members of the NMDA receptor, known as NR3 subunits, seem to be involved. Recently developed uncompetitive NMDA channel blockers such as memantine hold therapeutic promise because these agents are well tolerated clinically and might prove to be effective at protecting certain white matter elements from a variety of insults.
轴突、包裹它们的髓磷脂以及构成哺乳动物脑和脊髓白质的支持性神经胶质细胞,对于中枢神经系统的正常运作至关重要。中风、血管性痴呆、多发性硬化症、脑和脊髓创伤、HIV相关痴呆、早产儿脑室周围白质软化等常见人类疾病,以及看似传统的“灰质疾病”,如阿尔茨海默病和精神分裂症,都表现出白质病理变化,这些变化会导致发病和死亡。已表明N-甲基-D-天冬氨酸(NMDA)受体在介导少突胶质细胞和髓鞘的钙依赖性损伤中起重要作用;新发现的NMDA受体家族成员,即NR3亚基,似乎也参与其中。最近开发的非竞争性NMDA通道阻滞剂,如美金刚,具有治疗前景,因为这些药物在临床上耐受性良好,可能证明对保护某些白质成分免受各种损伤有效。