Source:http://linkedlifedata.com/resource/pubmed/id/10656628
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2000-2-17
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pubmed:abstractText |
The present study was performed to determine whether excess hepatic iron modulates the cancer-initiating and promoting properties of FB1. Thirty-eight male F344 rats were divided into four dietary treatment groups: (i) control diet (AIN, n = 8); (ii) FB1 250 mg/kg diet (FB1, n = 10); (iii) 1-2% carbonyl iron (CI, n = 10); or (iv) FB1 plus iron loading (FB1/CI, n = 10) for 5 weeks (2 x 2 factorial design). Hepatic iron concentrations in iron-loaded animals at 5 weeks were 444 +/- 56 (CI) and 479 +/- 80 micromol/g dry weight (FB1/CI) (mean +/- SEM). All the FB1-fed rats, in the presence or absence of CI, developed a toxic hepatitis with a 4-fold rise in serum alanine transaminase (ALT) levels. FB1 appeared to augment iron-induced hepatic lipid peroxidation, as measured by the generation of thiobarbituric acid reacting substances (TBARS) in liver homogenates (P < 0.0001). Morphometric analysis showed that FB1 caused a significantly greater mean +/- SEM number of 'enzyme-altered' foci and nodules per cm2 (5.34 +/- 1.42 vs. 1.50 +/- 0.52, P < 0.05), as well as a greater area (%) of liver occupied by foci and nodules (0.33 +/- 0.12% vs. 0.05 +/- 0.03%, P < 0.001), compared with FB1/CI. The addition of FB1 to dietary iron loading caused a shift in distribution of iron from hepatocytes to Kupffer cells, probably due to phagocytosis of necrotic iron-loaded hepatocytes. In conclusion, (i) FB1 appears to cause toxicity in the liver independently from effects on lipid peroxidation; (ii) FB1 has a potentiating effect on iron-induced lipid peroxidation; and (iii) dietary iron loading appears to protect against the cancer promoting properties of FB1, possibly due to a stimulatory effect of iron on hepatocyte regeneration.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carboxylic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens, Environmental,
http://linkedlifedata.com/resource/pubmed/chemical/Fumonisins,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione S-Transferase pi,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Transferase,
http://linkedlifedata.com/resource/pubmed/chemical/Gstp1 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/fumonisin B1
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0304-3835
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
146
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
207-15
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:10656628-Animals,
pubmed-meshheading:10656628-Carboxylic Acids,
pubmed-meshheading:10656628-Carcinogens, Environmental,
pubmed-meshheading:10656628-Fumonisins,
pubmed-meshheading:10656628-Glutathione S-Transferase pi,
pubmed-meshheading:10656628-Glutathione Transferase,
pubmed-meshheading:10656628-Iron Overload,
pubmed-meshheading:10656628-Isoenzymes,
pubmed-meshheading:10656628-Lipid Peroxidation,
pubmed-meshheading:10656628-Liver,
pubmed-meshheading:10656628-Liver Neoplasms, Experimental,
pubmed-meshheading:10656628-Male,
pubmed-meshheading:10656628-Organ Size,
pubmed-meshheading:10656628-Rats,
pubmed-meshheading:10656628-Rats, Inbred F344,
pubmed-meshheading:10656628-Weight Gain
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pubmed:year |
1999
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pubmed:articleTitle |
The effects of dietary iron overload on fumonisin B1-induced cancer promotion in the rat liver.
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pubmed:affiliation |
MRC/UCT Liver Research Centre, University of Cape Town, South Africa. eric_lemmer@nih.gov
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pubmed:publicationType |
Journal Article
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