Source:http://linkedlifedata.com/resource/pubmed/id/11181109
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2001-2-22
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pubmed:abstractText |
Peroxisomeproliferators (PPs) cause hepatomegaly, peroxisome proliferation, and hepatocarcinogenesis in rats and mice. Conversely, hamsters are less responsive to these compounds. PPs increase peroxisomal beta-oxidation and P4504A subfamily activity, which has been hypothesized to result in oxidative stress. We hypothesized that differential modulation of glutathione-related defenses could account for the resulting difference in species susceptibility following PP administration. Accordingly, we measured glutathione S-transferase (GST), glutathione peroxidase (GPx), and glutathione reductase (GR) activities, and total glutathione (GSH) in male Sprague-Dawley rats and Syrian hamsters fed two doses of three known peroxisome proliferators [dibutylphthalate (DBP), gemfibrozil, and Wy-14,643] for 6, 34, or 90 days. In rats, decreases in GR, GST, and selenium-dependent GPx were observed following PP treatment at various time points. In hamsters, we observed higher basal levels of activities for GR, GST, and selenium-dependent GPx compared to rats. In addition, hamsters showed decreases in GR and GST activities following PP treatment. Interestingly, selenium-dependent GPx activity was increased in hamsters following treatment with Wy-14,643 and DBP. Treatment for 90 days with Wy-14,643 resulted in no change in GPx1 mRNA in rats and increased GPx1 mRNA in hamsters. Sporadic changes in total GSH and selenium-independent GPx were observed in both species. This divergence in the hydrogen peroxide detoxification ability between rats and hamsters could be a contributing factor in the proposed oxidative stress mechanism of PPs observed in responsive and nonresponsive species.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Dibutyl Phthalate,
http://linkedlifedata.com/resource/pubmed/chemical/Gemfibrozil,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Peroxidase,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Reductase,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Transferase,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrogen Peroxide,
http://linkedlifedata.com/resource/pubmed/chemical/Peroxisome Proliferators,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidines,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/pirinixic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0041-008X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
171
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
27-37
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11181109-Animals,
pubmed-meshheading:11181109-Cricetinae,
pubmed-meshheading:11181109-Dibutyl Phthalate,
pubmed-meshheading:11181109-Gemfibrozil,
pubmed-meshheading:11181109-Glutathione,
pubmed-meshheading:11181109-Glutathione Peroxidase,
pubmed-meshheading:11181109-Glutathione Reductase,
pubmed-meshheading:11181109-Glutathione Transferase,
pubmed-meshheading:11181109-Hydrogen Peroxide,
pubmed-meshheading:11181109-Male,
pubmed-meshheading:11181109-Mesocricetus,
pubmed-meshheading:11181109-Peroxisome Proliferators,
pubmed-meshheading:11181109-Pyrimidines,
pubmed-meshheading:11181109-RNA, Messenger,
pubmed-meshheading:11181109-Rats,
pubmed-meshheading:11181109-Rats, Sprague-Dawley,
pubmed-meshheading:11181109-Species Specificity
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pubmed:year |
2001
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pubmed:articleTitle |
Effects of peroxisome proliferators on glutathione and glutathione-related enzymes in rats and hamsters.
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pubmed:affiliation |
Graduate Center for Toxicology, University of Kentucky, Lexington, Kentucky 40506, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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