Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:15201437rdf:typepubmed:Citationlld:pubmed
pubmed-article:15201437lifeskim:mentionsumls-concept:C0026339lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C0034721lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C0034693lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C0026336lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C1512409lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C1704686lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C2349975lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C0064401lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C0058157lld:lifeskim
pubmed-article:15201437lifeskim:mentionsumls-concept:C1627358lld:lifeskim
pubmed-article:15201437pubmed:issue1lld:pubmed
pubmed-article:15201437pubmed:dateCreated2004-8-12lld:pubmed
pubmed-article:15201437pubmed:abstractTextKojic acid (KA) has been used as a food additive for preventing enzymatic browning of crustaceans and as a cosmetic agent for skin whitening. In the present experiments, effects of KA on the induction of hepatic pre-neoplastic lesions in N-bis(2-hydroxypropyl)nitrosamine-initiated (experiment 1) and non-initiated (experiment 2) models, and its promoting influence in a medium-term liver bioassay (experiment 3) were investigated at dietary doses of up to 2% in male F344 rats. In experiment 1, 2% KA feeding induced significant increases in numbers (22.3 +/- 13.0 vs 8.5 +/- 3.4 in the 0%) and areas (0.37 +/- 0.29 vs 0.05 +/- 0.03 in the 0%) of glutathione-S-transferase P form (GST-P)-positive foci and toxic changes such as vacuolation of hepatocytes and microgranulomas. The development of GST-P-positive foci was pronounced in the animals with hepatocellular toxic changes. In experiment 2, numbers (0.65 +/- 0.57 vs 0.17 +/- 0.28 in the 0%) and areas (0.005 +/- 0.005 vs 0.0007 +/- 0.0012 in the 0%) of GST-P-positive foci and hepatocellular proliferating cell nuclear antigen (PCNA) expression (3.8 +/- 2.3 vs 2.6 +/- 0.7 in the 0%) were significantly increased by the 2% treatment. The PCNA-positive hepatocytes were abundantly localized around the vacuolated and granulomatous legions in both experiments 1 and 2. In experiment 3, significant increases in numbers (16.9 +/- 3.2 vs 8.4 +/- 2.7 in the 0%) and areas (1.62 +/- 0.39 vs 0.77 +/- 0.34 in the 0%) of GST-P-positive foci were again observed with 2% KA. These results demonstrate tumor-promoting and possible hepatocarcinogenic activity of KA at 2%, but the carcinogenic potential is likely to be weak. This study also indicated that enhanced replication of hepatocytes related to toxic changes might be involved as an underlying mechanism.lld:pubmed
pubmed-article:15201437pubmed:languageenglld:pubmed
pubmed-article:15201437pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:citationSubsetIMlld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15201437pubmed:statusMEDLINElld:pubmed
pubmed-article:15201437pubmed:monthSeplld:pubmed
pubmed-article:15201437pubmed:issn1096-6080lld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:ImaiToshioTlld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:TamuraToruTlld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:TakizawaTamot...lld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:UedaMakotoMlld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:HiroseMasaoMlld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:MitsumoriKuni...lld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:OnoseJun-ichi...lld:pubmed
pubmed-article:15201437pubmed:authorpubmed-author:IzumiKeisukeKlld:pubmed
pubmed-article:15201437pubmed:issnTypePrintlld:pubmed
pubmed-article:15201437pubmed:volume81lld:pubmed
pubmed-article:15201437pubmed:ownerNLMlld:pubmed
pubmed-article:15201437pubmed:authorsCompleteYlld:pubmed
pubmed-article:15201437pubmed:pagination43-9lld:pubmed
pubmed-article:15201437pubmed:dateRevised2010-9-17lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:meshHeadingpubmed-meshheading:15201437...lld:pubmed
pubmed-article:15201437pubmed:year2004lld:pubmed
pubmed-article:15201437pubmed:articleTitleEnhancement of hepatocarcinogenesis by kojic acid in rat two-stage models after initiation with N-bis(2-hydroxypropyl)nitrosamine or N-diethylnitrosamine.lld:pubmed
pubmed-article:15201437pubmed:affiliationDivision of Pathology, National Institute of Health Sciences, Tokyo 158-8501, Japan.lld:pubmed
pubmed-article:15201437pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15201437pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed