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阿尔茨海默病及其他神经退行性痴呆中的一氧化氮通路

Nitric oxide pathways in Alzheimer's disease and other neurodegenerative dementias.

作者信息

Togo Takashi, Katsuse Omi, Iseki Eizo

机构信息

Department of Psychiatry, Yokohama City University School of Medicine, Japan.

出版信息

Neurol Res. 2004 Jul;26(5):563-6. doi: 10.1179/016164104225016236.

Abstract

Nitric oxide (NO) is an enzymatic product of nitric oxide synthase (NOS). NO has significant physiological functions and an increasing body of evidence suggests that NO pathways are implicated in a number of neurological disorders, including Alzheimer's disease (AD) and other neurodegenerative dementias. NO is continuously released by endothelial cells in the vascular system, whereas advanced age in the presence of vascular risk factor causes a decrease in cerebral blood flow, involving microvasculopathy with impaired NO release, which in turn results in regional metabolic dysfunction. This finding suggests that vascular pathology plays a crucial role in the pathogenesis of so-called neurodegenerative dementias. Inflammatory responses are commonly found in the brain under a variety of neurodegenerative dementias, including AD and dementia with Lewy bodies, in which up-regulation of NOS expression, suggesting overproduction of NO, is found in neurons and glia. NO is thought to be involved in such neuroinflammation due to its free radical properties, which compromise cellular integrity and viability via mitochondrial damage. Further studies to elucidate NO pathways in neurodegenerative dementias could lead to a better understanding of their pathogenesis and improved therapeutic strategies, and therefore are certainly warranted.

摘要

一氧化氮(NO)是一氧化氮合酶(NOS)的酶促产物。NO具有重要的生理功能,越来越多的证据表明,NO通路与包括阿尔茨海默病(AD)和其他神经退行性痴呆在内的多种神经系统疾病有关。血管系统中的内皮细胞持续释放NO,而存在血管危险因素时的高龄会导致脑血流量减少,涉及微血管病变且NO释放受损,进而导致局部代谢功能障碍。这一发现表明血管病理在所谓神经退行性痴呆的发病机制中起关键作用。在包括AD和路易体痴呆在内的多种神经退行性痴呆中,大脑中普遍存在炎症反应,其中在神经元和胶质细胞中发现NOS表达上调,提示NO产生过多。由于其自由基特性,NO被认为参与了这种神经炎症,它通过线粒体损伤损害细胞完整性和活力。进一步研究阐明神经退行性痴呆中的NO通路可能会更好地理解其发病机制并改进治疗策略,因此确实有必要进行研究。

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