Transcriptome analyses demonstrate that Peroxisome Proliferator-Activated Receptor α (PPARα) activity of an ultraviolet absorber, 2-(2’-hydroxy-3’,5’-di-tert-butylphenyl)benzotriazole, as possible mechanism of their toxicity and the gender differences

• Published in: Journal of toxicological sciences 2016/10/01, Vol.41(5), pp.693-700
• Main Authors: Hirata-Koizumi, Mutsuko, Ise, Ryota, Kato, Hirohito, Matsuyama, Takashi, Nishimaki-Mogami, Tomoko, Takahashi, Mika, Ono, Atsushi, Ema, Makoto, Hirose, Akihiko
• Format: Article
• Language: English
• Subjects: 2-(2′-hydroxy-3′,5′-di-tert-butylphenyl)benzotriazole; Agonists; Animals; Benzotriazole; Benzotriazole UV-stabilizer; Chemical and Drug Induced Liver Injury - etiology; Chemical and Drug Induced Liver Injury - genetics; Chemical and Drug Induced Liver Injury - metabolism; Computational Biology; Databases, Genetic; Dental materials; DNA microarrays; Female; Females; Fenofibrate; Gemfibrozil; Gender; Gender aspects; Gender differences; Gene expression; Gene Expression Profiling - methods; Gene Expression Regulation, Developmental; Hepatotoxicity; Hypertrophy; Ingestion; Irradiation; Liver - drug effects; Liver - metabolism; Male; Males; Necrosis; Oligonucleotide Array Sequence Analysis; Peroxisome proliferator-activated receptor α; Peroxisome proliferator-activated receptors; Phenotypes; PPAR alpha - agonists; PPAR alpha - metabolism; Rats, Sprague-Dawley; RNA, Messenger - genetics; RNA, Messenger - metabolism; Rodents; Sex; Sex differences; Sex Factors; Sex-related difference in toxicity; Time Factors; Toxicity; Triazoles - toxicity; Ultraviolet radiation
• ISSN: 0388-1350; 1880-3989
• DOI: 10.2131/jts.41.693

2-(2′-Hydroxy-3′,5′-di-tert-butylphenyl)benzotriazole (HDBB), the Benzotriazole UV-stabilizer (BUVSs) known as UV-320, is widely used in plastic materials for protection against UV-irradiation. Previously, we reported that oral ingestion of HDBB induce hepatotoxicity including hepatocyte hypertrophy and necrosis in rats and, males was more susceptible compared with females in young rats while no sex-related difference was observed in preweaning rats. Phenotypes observed in our previous study imply involvement of peroxisome proliferator-activated receptor (PPAR) α in HDBB hepatotoxicity, however, direct evidence that HDBB can activate PPARα has not been provided and the mechanism which underlying the gender difference of HDBB hepatotoxicity was not clearly elucidated. Here, we conduct transcriptome analysis using microarray expression profiles in the livers of rats administered HDBB. PPARα agonist activity of HDBB was elucidated by comparison with gene expression data of typical PPARα agonist, i.e. clofibrate, WY-14643, gemfibrozil, and fenofibrate, from TG GATEs database. Moreover, we analyzed for PPARα mRNA expression in the liver of developing male and female rats. PPARα mRNA expression level was higher in males than in females on postnatal days (PNDs) 28 and 35, whereas no sex-related difference was found on PNDs 7 and 22. These results suggest that HDBB exerts its hepatotoxicity through the PPARα signal pathway and the sex-related difference in PPARα expression may contribute to the sex-related difference in susceptibility to hepatotoxicity.