Iron chelation and neuroprotection in neurodegenerative diseases

被引:66
|
作者
Li, Xuping [1 ]
Jankovic, Joseph [1 ]
Le, Weidong [1 ]
机构
[1] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA
关键词
Iron chelation; Neuroprotection; Parkinson's disease; Alzheimer's disease; Amyotrophic lateral sclerosis; DOPAMINE NEURON DEGENERATION; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; TRANSGENIC MOUSE; AMYLOID-BETA; MODEL; LOCALIZATION; ANTIOXIDANTS; CONTRIBUTES;
D O I
10.1007/s00702-010-0518-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Iron is an essential element for multiple functions of the brain. Maintenance of iron homeostasis involves regulation of iron influx, iron efflux and iron storage. Mismanagement of brain iron has been implicated in neuronal injury and death in several neurodegenerative diseases, such as Parkinson's disease (PD), Alzheimer's disease (PD) and Amyotrophic lateral sclerosis (ALS). Multiple iron chelators have been shown neuroprotective and neurorestorative in these diseases, suggesting that iron chelation might be a promising therapeutics. In this paper, we briefly review the new findings of biological function of several molecules that regulate iron homeostasis in the brain, the possible role of iron mismanagement in the pathogenesis of PD, AD and ALS, and then discuss the putative mechanisms for current available iron chelators as potential therapeutics for neurodegenerative diseases.
引用
收藏
页码:473 / 477
页数:5
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