Biometals and Their Therapeutic Implications in Alzheimer's Disease

被引:117
作者
Ayton, Scott [1 ]
Lei, Peng [1 ]
Bush, Ashley I. [1 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Oxidat Biol Unit, Parkville, Vic 3052, Australia
关键词
Alzheimer's disease; Iron; Copper; Zinc; Chelation therapy; AMYLOID PRECURSOR PROTEIN; A-BETA OLIGOMERS; GLYCOGEN-SYNTHASE KINASE-3-BETA; D-ASPARTATE RECEPTOR; TAU-PHOSPHORYLATION; TRANSGENIC MICE; MOUSE MODEL; LIPID-PEROXIDATION; OXIDATIVE STRESS; CELL-DEATH;
D O I
10.1007/s13311-014-0312-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
No disease modifying therapy exists for Alzheimer's disease (AD). The growing burden of this disease to our society necessitates continued investment in drug development. Over the last decade, multiple phase 3 clinical trials testing drugs that were designed to target established disease mechanisms of AD have all failed to benefit patients. There is, therefore, a need for new treatment strategies. Changes to the transition metals, zinc, copper, and iron, in AD impact on the molecular mechanisms of disease, and targeting these metals might be an alternative approach to treat the disease. Here we review how metals feature in molecular mechanisms of AD, and we describe preclinical and clinical data that demonstrate the potential for metal-based drug therapy.
引用
收藏
页码:109 / 120
页数:12
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