Source:http://linkedlifedata.com/resource/pubmed/id/18159970
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-12-27
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pubmed:abstractText |
Peroxidation products formed from polyunsaturated lipids have DNA damaging potential. 4-oxo-2-hexenal (4-OHE), generated by the oxidation of omega-3 fatty acids, has been demonstrated to be mutagenic in vitro as assessed in the Ames test. To examine the carcinogenic risk of 4-OHE in vivo, initiation activity was investigated in a five-week liver assay, established to be effective for screening of carcinogenic potential of mutagens. Seven-week-old male F344 rats underwent two-thirds partial hepatectomy (PH) and were administered 4-OHE intragastrically at doses of 128, 80, 64, 40, 32, 20, or 0 mg/kg body weight (b.w.) at 18 hours thereafter, then being fed on diet containing 0.015% 2-acetylaminofluorene from weeks 2 to 4. All rats were given with 0.8 ml/kg b.w. CCl4 at week 3. At week 5, all survivors were sacrificed and initiation activity was assessed with reference to induction of glutathione S-transferase placental form (GST-P) positive foci in the liver. Mortality was significantly increased to 72.7% in the 128 mg/kg b.w. dose group compared with 0.9% in the control group. However, the average number of GST-P positive foci in the "128" dose group was 3.26-/+1.66 foci/cm2, not significantly different from the control value (2.78?1.33). Areas of GST-P positive foci were also similar (1.11-/+0.5 and 1.53-/+1.33 mm2/cm2 in "128" and the control groups, respectively). These results showed 4-OHE to have no significant initiation activity in.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1513-7368
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pubmed:author |
pubmed-author:BanHisayoH,
pubmed-author:HirataAkihiroA,
pubmed-author:KasaiHiroshiH,
pubmed-author:KawaiKazuakiK,
pubmed-author:MasegiToshiakiT,
pubmed-author:SakaiHirokiH,
pubmed-author:TakasuShinjiS,
pubmed-author:TatematsuMasaeM,
pubmed-author:ToyodaTakeshiT,
pubmed-author:TsukamotoTetsuyaT,
pubmed-author:YanaiTokumaT
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pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
372-4
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pubmed:meshHeading |
pubmed-meshheading:18159970-Aldehydes,
pubmed-meshheading:18159970-Animals,
pubmed-meshheading:18159970-Dose-Response Relationship, Drug,
pubmed-meshheading:18159970-Fatty Acids, Omega-3,
pubmed-meshheading:18159970-Lipid Peroxidation,
pubmed-meshheading:18159970-Liver,
pubmed-meshheading:18159970-Male,
pubmed-meshheading:18159970-Rats,
pubmed-meshheading:18159970-Rats, Inbred F344
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pubmed:articleTitle |
Lack of initiation activity of 4-oxo-2-hexenal, a peroxidation product generated from omega-3 polyunsaturated fatty acids, in an in vivo five-week liver assay.
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pubmed:affiliation |
Division of Oncological Pathology, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan.
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pubmed:publicationType |
Journal Article,
Evaluation Studies
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