Differential response to trichloroethylene-induced hepatosteatosis in wild-type and pparα-humanized mice

Doni Hikmat Ramdhan, Michihiro Kamijima, Dong Wang, Yuki Ito, Hisao Naito, Yukie Yanagiba, Yumi Hayashi, Naoki Tanaka, Toshifumi Aoyama, Frank J. Gonzalez, Tamie Nakajima

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30 Citations (Scopus)

Abstract

Background: Trichloroacetic acid, an oxidative metabolite of trichloroethylene (TRI), is a ligand of the peroxisome proliferator-activated receptor α (PPAR) α, which is involved in lipid homeostasis and anti-inflammation. Objective: We examined the role of mouse and human PPARα in TRI-induced hepatic steatosis and toxicity. Methods: Male wild-type (mPPARα), Pparα-null, and humanized PPARα (hPPARα) mice on an Sv/129 background were exposed via inhalation to 0, 1,000, and 2,000 ppm TRI for 8 hr/day for 7 days. We assessed TRI-induced steatosis or hepatic damage through biochemical and histopathological measurements. Results: Plasma alanine aminotransferase and aspartate aminotransferase activities increased in all mouse lines after exposure to 1,000 and 2,000 ppm TRI. Exposure induced hepatocyte necrosis and inflammatory cells in all mouse lines, but hepatic lipid accumulation was observed only in Pparα-null and hPPARα mice. No differences were observed in TRI-mediated induction of hepatic PPARα target genes except for a few genes that differed between mPPARα and hPPARα mice. However, TRI significantly increased expression of triglyceride (TG)-synthesizing enzymes, diacylglicerol acyltransferases, and PPARγ in Pparα-null and hPPARα mice, which may account for the increased TG in their livers. TRI exposure elevated nuclear factor-kappa B (NFκB) p52 mRNA and protein in all mice regardless of PPARα genotype. Conclusions: NFκB-p52 is a candidate molecular marker for inflammation caused by TRI, and PPARα may be involved in TRI-induced hepatosteatosis. However, human PPARα may afford only weak protection against TRI-mediated effects compared with mouse PPARα.

Original languageEnglish
Pages (from-to)1557-1563
Number of pages7
JournalEnvironmental Health Perspectives
Volume118
Issue number11
DOIs
Publication statusPublished - 01-11-2010

All Science Journal Classification (ASJC) codes

  • Public Health, Environmental and Occupational Health
  • Health, Toxicology and Mutagenesis

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    Ramdhan, D. H., Kamijima, M., Wang, D., Ito, Y., Naito, H., Yanagiba, Y., Hayashi, Y., Tanaka, N., Aoyama, T., Gonzalez, F. J., & Nakajima, T. (2010). Differential response to trichloroethylene-induced hepatosteatosis in wild-type and pparα-humanized mice. Environmental Health Perspectives, 118(11), 1557-1563. https://doi.org/10.1289/ehp.1001928