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Mechanisms of brain iron transport: insight into neurodegeneration and CNS disorders.
- Source :
-
Future medicinal chemistry [Future Med Chem] 2010 Jan; Vol. 2 (1), pp. 51-64. - Publication Year :
- 2010
-
Abstract
- Trace metals such as iron, copper, zinc, manganese, and cobalt are essential cofactors for many cellular enzymes. Extensive research on iron, the most abundant transition metal in biology, has contributed to an increased understanding of the molecular machinery involved in maintaining its homeostasis in mammalian peripheral tissues. However, the cellular and intercellular iron transport mechanisms in the central nervous system (CNS) are still poorly understood. Accumulating evidence suggests that impaired iron metabolism is an initial cause of neurodegeneration, and several common genetic and sporadic neurodegenerative disorders have been proposed to be associated with dysregulated CNS iron homeostasis. This review aims to provide a summary of the molecular mechanisms of brain iron transport. Our discussion is focused on iron transport across endothelial cells of the blood-brain barrier and within the neuro- and glial-vascular units of the brain, with the aim of revealing novel therapeutic targets for neurodegenerative and CNS disorders.
- Subjects :
- Animals
Biological Transport
Blood-Brain Barrier metabolism
Brain cytology
Brain pathology
Central Nervous System Diseases pathology
Central Nervous System Diseases physiopathology
Central Nervous System Diseases therapy
Homeostasis
Humans
Neurodegenerative Diseases pathology
Neurodegenerative Diseases physiopathology
Neurodegenerative Diseases therapy
Neuroglia metabolism
Neurons metabolism
Oxidative Stress
Trace Elements metabolism
Brain metabolism
Central Nervous System Diseases metabolism
Iron metabolism
Neurodegenerative Diseases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1756-8927
- Volume :
- 2
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Future medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 20161623
- Full Text :
- https://doi.org/10.4155/fmc.09.140