rdf:type |
|
lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2010-7-19
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pubmed:abstractText |
Enhancement of the anti-oxidant metabolism of Leishmania parasites, dependent upon the unique dithiol trypanothione, has been implicated in laboratory-generated antimony resistance. Here, the role of the trypanothione-dependent anti-oxidant pathway is studied in antimony-resistant clinical isolates. Elevated levels of tryparedoxin and tryparedoxin peroxidase, key enzymes in hydroperoxide detoxification, were observed in antimonial resistant parasites resulting in an increased metabolism of peroxides. These data suggest that enhanced anti-oxidant defences may play a significant role in clinical resistance to antimonials.
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pubmed:grant |
|
pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1872-9428
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pubmed:author |
|
pubmed:copyrightInfo |
Copyright 2010 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
173
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
162-4
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pubmed:meshHeading |
pubmed-meshheading:20553768-Antimony,
pubmed-meshheading:20553768-Antiprotozoal Agents,
pubmed-meshheading:20553768-Drug Resistance,
pubmed-meshheading:20553768-Humans,
pubmed-meshheading:20553768-Leishmania donovani,
pubmed-meshheading:20553768-Leishmaniasis, Visceral,
pubmed-meshheading:20553768-Peroxidases,
pubmed-meshheading:20553768-Peroxides,
pubmed-meshheading:20553768-Protozoan Proteins,
pubmed-meshheading:20553768-Thioredoxins
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pubmed:year |
2010
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pubmed:articleTitle |
Elevated levels of tryparedoxin peroxidase in antimony unresponsive Leishmania donovani field isolates.
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pubmed:affiliation |
Division of Biological Chemistry and Drug Discovery, College of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH Scotland, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|