Oxyferriscorbone elevates the total iron content of blood but not brain.
Identifieur interne : 004F74 ( PubMed/Checkpoint ); précédent : 004F73; suivant : 004F75Oxyferriscorbone elevates the total iron content of blood but not brain.
Auteurs : D T Dexter [Royaume-Uni] ; P. Jenner ; C D MarsdenSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1989.
English descriptors
- KwdEn :
- 2,3-Diketogulonic Acid (pharmacology), Alloxan (pharmacology), Animals, Blood-Brain Barrier (drug effects), Brain (drug effects), Brain (metabolism), Copper (blood), Drug Combinations (pharmacology), Ferric Compounds (pharmacology), Infusions, Intravenous, Iron (blood), Male, Rats, Rats, Inbred Strains, Sugar Acids (pharmacology), Zinc (blood).
- MESH :
- chemical , blood : Copper, Iron, Zinc.
- chemical , pharmacology : 2,3-Diketogulonic Acid, Alloxan, Drug Combinations, Ferric Compounds, Sugar Acids.
- drug effects : Blood-Brain Barrier, Brain.
- metabolism : Brain.
- Animals, Infusions, Intravenous, Male, Rats, Rats, Inbred Strains.
Abstract
Following the intravenous infusion of oxyferriscorbone into the tail vein of the rat, the blood and brain metal ion content was measured over the following 72 h period. Administration of oxyferriscorbone increased the total iron content of blood for up to 24 h following intravenous infusion. In contrast, there was no increase in the total iron content of the cerebellum or striatum. Overall, there was no change in total zinc or copper content of the blood or brain following oxyferriscorbone administration. The effect of oxyferriscorbone in Parkinson's disease may not be related to any alteration in total iron content of the brain.
DOI: 10.1002/mds.870040209
PubMed: 2733708
Affiliations:
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pubmed:2733708Le document en format XML
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<author><name sortKey="Dexter, D T" sort="Dexter, D T" uniqKey="Dexter D" first="D T" last="Dexter">D T Dexter</name>
<affiliation wicri:level="3"><nlm:affiliation>University Department of Neurology, Institute of Psychiatry, London, U.K.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>University Department of Neurology, Institute of Psychiatry, London</wicri:regionArea>
<placeName><settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
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<author><name sortKey="Jenner, P" sort="Jenner, P" uniqKey="Jenner P" first="P" last="Jenner">P. Jenner</name>
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<author><name sortKey="Marsden, C D" sort="Marsden, C D" uniqKey="Marsden C" first="C D" last="Marsden">C D Marsden</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Oxyferriscorbone elevates the total iron content of blood but not brain.</title>
<author><name sortKey="Dexter, D T" sort="Dexter, D T" uniqKey="Dexter D" first="D T" last="Dexter">D T Dexter</name>
<affiliation wicri:level="3"><nlm:affiliation>University Department of Neurology, Institute of Psychiatry, London, U.K.</nlm:affiliation>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>2,3-Diketogulonic Acid (pharmacology)</term>
<term>Alloxan (pharmacology)</term>
<term>Animals</term>
<term>Blood-Brain Barrier (drug effects)</term>
<term>Brain (drug effects)</term>
<term>Brain (metabolism)</term>
<term>Copper (blood)</term>
<term>Drug Combinations (pharmacology)</term>
<term>Ferric Compounds (pharmacology)</term>
<term>Infusions, Intravenous</term>
<term>Iron (blood)</term>
<term>Male</term>
<term>Rats</term>
<term>Rats, Inbred Strains</term>
<term>Sugar Acids (pharmacology)</term>
<term>Zinc (blood)</term>
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<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Copper</term>
<term>Iron</term>
<term>Zinc</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>2,3-Diketogulonic Acid</term>
<term>Alloxan</term>
<term>Drug Combinations</term>
<term>Ferric Compounds</term>
<term>Sugar Acids</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Blood-Brain Barrier</term>
<term>Brain</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brain</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Infusions, Intravenous</term>
<term>Male</term>
<term>Rats</term>
<term>Rats, Inbred Strains</term>
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<front><div type="abstract" xml:lang="en">Following the intravenous infusion of oxyferriscorbone into the tail vein of the rat, the blood and brain metal ion content was measured over the following 72 h period. Administration of oxyferriscorbone increased the total iron content of blood for up to 24 h following intravenous infusion. In contrast, there was no increase in the total iron content of the cerebellum or striatum. Overall, there was no change in total zinc or copper content of the blood or brain following oxyferriscorbone administration. The effect of oxyferriscorbone in Parkinson's disease may not be related to any alteration in total iron content of the brain.</div>
</front>
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<DateCreated><Year>1989</Year>
<Month>07</Month>
<Day>17</Day>
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<DateCompleted><Year>1989</Year>
<Month>07</Month>
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<DateRevised><Year>2013</Year>
<Month>11</Month>
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<Issue>2</Issue>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Oxyferriscorbone elevates the total iron content of blood but not brain.</ArticleTitle>
<Pagination><MedlinePgn>176-82</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Following the intravenous infusion of oxyferriscorbone into the tail vein of the rat, the blood and brain metal ion content was measured over the following 72 h period. Administration of oxyferriscorbone increased the total iron content of blood for up to 24 h following intravenous infusion. In contrast, there was no increase in the total iron content of the cerebellum or striatum. Overall, there was no change in total zinc or copper content of the blood or brain following oxyferriscorbone administration. The effect of oxyferriscorbone in Parkinson's disease may not be related to any alteration in total iron content of the brain.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Dexter</LastName>
<ForeName>D T</ForeName>
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<AffiliationInfo><Affiliation>University Department of Neurology, Institute of Psychiatry, London, U.K.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Jenner</LastName>
<ForeName>P</ForeName>
<Initials>P</Initials>
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<Author ValidYN="Y"><LastName>Marsden</LastName>
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<Initials>CD</Initials>
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<affiliations><list><country><li>Royaume-Uni</li>
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