Neurodegenerative disease and iron storage in the brain
Iron is very important for normal regulation of various metabolic pathways. Neurons store iron in the form of ferrous ion or neuromelanin. In specific disorders the axonal transport of iron is impaired, leading to iron deposition which in the presence of reactive oxygen species results in neurodegen...
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Veröffentlicht in: | Current opinion in neurology 2004-08, Vol.17 (4), p.437-442 |
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description | Iron is very important for normal regulation of various metabolic pathways. Neurons store iron in the form of ferrous ion or neuromelanin. In specific disorders the axonal transport of iron is impaired, leading to iron deposition which in the presence of reactive oxygen species results in neurodegeneration.
Recent developments in genetics, including the finding of mutations in the pantothenate kinase gene and ferritin light chain gene, have demonstrated a direct relationship between the presence of a mutation in the iron-regulatory pathways and iron deposition in the brain resulting in neurodegeneration. These two disorders now add to our understanding of the mechanism of disease due to dysfunction of iron-regulatory pathways. In addition to these disorders there may be several other mutations of iron-regulatory genes or related genes that are yet to be found. The animal models of disease have also added value to this area.
In this review we provide a summary of recent developments in the field of movement disorders with abnormalities in iron transport, and the current evidence in neurodegenerative disorders such as Parkinson's disease. |
doi_str_mv | 10.1097/01.wco.0000137534.61244.d1 |
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Recent developments in genetics, including the finding of mutations in the pantothenate kinase gene and ferritin light chain gene, have demonstrated a direct relationship between the presence of a mutation in the iron-regulatory pathways and iron deposition in the brain resulting in neurodegeneration. These two disorders now add to our understanding of the mechanism of disease due to dysfunction of iron-regulatory pathways. In addition to these disorders there may be several other mutations of iron-regulatory genes or related genes that are yet to be found. The animal models of disease have also added value to this area.
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Recent developments in genetics, including the finding of mutations in the pantothenate kinase gene and ferritin light chain gene, have demonstrated a direct relationship between the presence of a mutation in the iron-regulatory pathways and iron deposition in the brain resulting in neurodegeneration. These two disorders now add to our understanding of the mechanism of disease due to dysfunction of iron-regulatory pathways. In addition to these disorders there may be several other mutations of iron-regulatory genes or related genes that are yet to be found. The animal models of disease have also added value to this area.
In this review we provide a summary of recent developments in the field of movement disorders with abnormalities in iron transport, and the current evidence in neurodegenerative disorders such as Parkinson's disease.</description><subject>Animals</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Disease Models, Animal</subject><subject>Ferritins - deficiency</subject><subject>Ferritins - genetics</subject><subject>Humans</subject><subject>Iron - metabolism</subject><subject>Iron Metabolism Disorders - genetics</subject><subject>Iron Metabolism Disorders - metabolism</subject><subject>Iron Metabolism Disorders - physiopathology</subject><subject>Neurodegenerative Diseases - genetics</subject><subject>Neurodegenerative Diseases - metabolism</subject><subject>Neurodegenerative Diseases - physiopathology</subject><subject>Neurons - metabolism</subject><subject>Neurons - pathology</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - deficiency</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - genetics</subject><issn>1350-7540</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMtOwzAQRb0A0VL4BWSxYJfg8Ss1O1TxkirYwNqy40kxapNiJyD-nkArdTZ3c-4d6RByCawEZqprBuV33ZVsPBCVErLUwKUsAxyRKQjFikpJNiGnOX-MjOG6OiETUFyOsJmS6hmH1AVcYYvJ9fELaYgZXUbq2kBj6lqa-y65FdLY0v4dqU8utmfkuHHrjOf7nJG3-7vXxWOxfHl4Wtwui1qA6gtgWLGmlkEprrlXWHMNymiOnHPvJM597UWYCyG0N8I52RjvAJT3cq5Rihm52u1uU_c5YO7tJuYa12vXYjdkq7U2ihsxgjc7sE5dzgkbu01x49KPBWb_VFkGdlRlD6rsvyobYCxf7L8MfoPhUN17Er97q2eW</recordid><startdate>200408</startdate><enddate>200408</enddate><creator>Thomas, Madhavi</creator><creator>Jankovic, Joseph</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200408</creationdate><title>Neurodegenerative disease and iron storage in the brain</title><author>Thomas, Madhavi ; Jankovic, Joseph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-10e70fc4d55262b5ec2615962e222ba4e8bcb3d83336b93aa4f9ba115bb486e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Brain - physiopathology</topic><topic>Disease Models, Animal</topic><topic>Ferritins - deficiency</topic><topic>Ferritins - genetics</topic><topic>Humans</topic><topic>Iron - metabolism</topic><topic>Iron Metabolism Disorders - genetics</topic><topic>Iron Metabolism Disorders - metabolism</topic><topic>Iron Metabolism Disorders - physiopathology</topic><topic>Neurodegenerative Diseases - genetics</topic><topic>Neurodegenerative Diseases - metabolism</topic><topic>Neurodegenerative Diseases - physiopathology</topic><topic>Neurons - metabolism</topic><topic>Neurons - pathology</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - deficiency</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomas, Madhavi</creatorcontrib><creatorcontrib>Jankovic, Joseph</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current opinion in neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomas, Madhavi</au><au>Jankovic, Joseph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurodegenerative disease and iron storage in the brain</atitle><jtitle>Current opinion in neurology</jtitle><addtitle>Curr Opin Neurol</addtitle><date>2004-08</date><risdate>2004</risdate><volume>17</volume><issue>4</issue><spage>437</spage><epage>442</epage><pages>437-442</pages><issn>1350-7540</issn><abstract>Iron is very important for normal regulation of various metabolic pathways. Neurons store iron in the form of ferrous ion or neuromelanin. In specific disorders the axonal transport of iron is impaired, leading to iron deposition which in the presence of reactive oxygen species results in neurodegeneration.
Recent developments in genetics, including the finding of mutations in the pantothenate kinase gene and ferritin light chain gene, have demonstrated a direct relationship between the presence of a mutation in the iron-regulatory pathways and iron deposition in the brain resulting in neurodegeneration. These two disorders now add to our understanding of the mechanism of disease due to dysfunction of iron-regulatory pathways. In addition to these disorders there may be several other mutations of iron-regulatory genes or related genes that are yet to be found. The animal models of disease have also added value to this area.
In this review we provide a summary of recent developments in the field of movement disorders with abnormalities in iron transport, and the current evidence in neurodegenerative disorders such as Parkinson's disease.</abstract><cop>England</cop><pmid>15247539</pmid><doi>10.1097/01.wco.0000137534.61244.d1</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Brain - metabolism Brain - pathology Brain - physiopathology Disease Models, Animal Ferritins - deficiency Ferritins - genetics Humans Iron - metabolism Iron Metabolism Disorders - genetics Iron Metabolism Disorders - metabolism Iron Metabolism Disorders - physiopathology Neurodegenerative Diseases - genetics Neurodegenerative Diseases - metabolism Neurodegenerative Diseases - physiopathology Neurons - metabolism Neurons - pathology Phosphotransferases (Alcohol Group Acceptor) - deficiency Phosphotransferases (Alcohol Group Acceptor) - genetics |
title | Neurodegenerative disease and iron storage in the brain |
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