TITLE

Possible involvement of genotoxic mechanisms in estragole-induced hepatocarcinogenesis in rats

AUTHOR(S)
Suzuki, Yuta; Umemura, Takashi; Hibi, Daisuke; Inoue, Tomoki; Jin, Meilan; Ishii, Yuji; Sakai, Hiroki; Nohmi, Takehiko; Yanai, Tokuma; Nishikawa, Akiyoshi; Ogawa, Kumiko
PUB. DATE
October 2012
SOURCE
Archives of Toxicology;Oct2012, Vol. 86 Issue 10, p1593
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Estragole (ES) is a natural organic compound used frequently as a flavoring food additive. Although it has been reported to be tumorigenic and induce DNA adducts in the mouse liver, there have been no reports regarding ES hepatocarcinogenicity in rats. In the current study, we therefore examined potent carcinogenicity, DNA adduct formation and in vivo genotoxicity of ES in the livers of wild and reporter gene-carrying F344 rats. Males were administered 600 mg/kg bw ES by gavage and sequentially sacrificed at weeks 4, 8 and 16 for GST-P and PCNA immunohistochemistry and measurement of ES-specific DNA adducts by LC-MS/MS in the livers. GST-P-positive foci increased with time in ES-treated rats from week 4, PCNA-labeling indices being similarly elevated at both weeks 4 and 8. ES-specific DNA adducts such as ES-3′- N-dG, 3′-8-dG and 3′- N-dA were consistently detected, particularly at week 4. In a second study, male F344 gpt delta rats were administered 0, 22, 66, 200 or 600 mg/kg bw ES for 4 weeks. Gpt mutant frequency in the liver was increased in a dose-dependent manner, with significance at 200 and 600 mg/kg bw in good correlation with PCNA-labeling indices. Mutation spectra analysis showed A:T to G:C transitions to be predominantly increased in line with the formation of ES-3′- N-dA or 3′-8-dG. These results indicate that ES could be a possible genotoxic hepatocarcinogen in the rat, at least when given at high doses.
ACCESSION #
79824272

 

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