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阿尔茨海默病中的能量代谢、氧化应激与神经元变性

Energy metabolism, oxidative stress and neuronal degeneration in Alzheimer's disease.

作者信息

Sims N R

机构信息

Department of Medical Biochemistry, School of Medicine, Flinders University, Adelaide, Australia.

出版信息

Neurodegeneration. 1996 Dec;5(4):435-40. doi: 10.1006/neur.1996.0059.

Abstract

Both altered energy metabolism and oxidative stress have been proposed to contribute to tissue damage in neurogenerative diseases. Animal models and cell culture studies provide evidence for a role of these processes in several forms of neuronal death. Reductions in the activities of some key mitochondrial enzymes have been found in autopsied brain in Alzheimer's disease. However, results obtained with biopsied brain tissue as well as assessments of metabolic rates for glucose in vivo indicate that a reduced functional capacity of mitochondria is probably not a general feature in the brain in Alzheimer's disease. These studies do not address the possibility that short-lived changes in energy metabolism affecting a small number of cells at any one time could be contributing to cell death. Several findings point to a moderate increase in oxidative damage in those areas of brain which are most severely affected in this disease, probably resulting from an increase in production of reactive oxygen species. Whether this is a contributor to neurodegeneration or a consequence of it remains unresolved.

摘要

能量代谢改变和氧化应激均被认为与神经退行性疾病中的组织损伤有关。动物模型和细胞培养研究为这些过程在几种形式的神经元死亡中的作用提供了证据。在阿尔茨海默病患者的尸检大脑中发现了一些关键线粒体酶的活性降低。然而,对活检脑组织的研究结果以及体内葡萄糖代谢率的评估表明,线粒体功能能力降低可能并非阿尔茨海默病大脑的普遍特征。这些研究并未探讨能量代谢的短期变化在任何时候影响少数细胞是否可能导致细胞死亡的可能性。几项研究结果表明,在该疾病中受影响最严重的大脑区域,氧化损伤有适度增加,这可能是由于活性氧产生增加所致。这是神经退行性变的一个促成因素还是其结果仍未解决。

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