Literature DB >> 21161300

Iron chelation and neuroprotection in neurodegenerative diseases.

Xuping Li1, Joseph Jankovic, Weidong Le.   

Abstract

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.

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Year:  2010        PMID: 21161300     DOI: 10.1007/s00702-010-0518-0

Source DB:  PubMed          Journal:  J Neural Transm (Vienna)        ISSN: 0300-9564            Impact factor:   3.575


  44 in total

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Review 9.  Ferritins: a family of molecules for iron storage, antioxidation and more.

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10.  Oxidative inactivation of mitochondrial aconitase results in iron and H2O2-mediated neurotoxicity in rat primary mesencephalic cultures.

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5.  Pathophysiology and treatment of neurodegeneration with brain iron accumulation in the pediatric population.

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6.  Targeting chelatable iron as a therapeutic modality in Parkinson's disease.

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Journal:  Curr Neurol Neurosci Rep       Date:  2016-01       Impact factor: 5.081

Review 8.  Excess iron harms the brain: the syndromes of neurodegeneration with brain iron accumulation (NBIA).

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Journal:  J Neural Transm (Vienna)       Date:  2012-12-02       Impact factor: 3.575

9.  Subchronic exposure to leachate activates key markers linked with neurological disorder in Wistar male rat.

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10.  Quercetin, chrysin, caffeic acid and ferulic acid ameliorate cyclophosphamide-induced toxicities in SH-SY5Y cells.

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