Aryl hydrocarbon receptor ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin enhances liver damage in bile duct-ligated mice

Jun Ozeki, Shigeyuki Uno, Michitaka Ogura, Mihwa Choi, Tetsuyo Maeda, Kenichi Sakurai, Sadanori Matsuo, Sadao Amano, Daniel W. Nebert, Makoto Makishima

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


The environmental pollutant 2,3,7,8-tetracholorodibenzo- p-dioxin (TCDD) is known to cause a wide variety of toxic effects, including hepatotoxicity, by way of the aryl hydrocarbon receptor (AHR). Although inducible expression of cytochrome P450 (CYP) 1A1 and CYP1A2 is associated with liver injury caused by high-dose TCDD, the specific role of the AHR-CYP1 cascade in hepatotoxicity remains unclear. We investigated the effects of AHR activation under conditions of cholestasis. We administered oral TCDD to mice at a dose that can effectively induce Cyp1 gene expression without overt liver toxicity and then ligated their bile ducts. TCDD pretreatment enhanced bile duct ligation (BDL)-induced increases in liver and plasma bile acids, bilirubin, and aminotransferases. Histology of TCDD-pretreated BDL mice revealed massive hepatic necrosis without any increase in number of apoptotic cells. Whereas induction of AHR-target genes by TCDD was observed similarly in sham-operated as well as in BDL mice, TCDD pretreatment of BDL mice altered the expression of hepatic genes involved in bile acid synthesis and transport. Increased plasma proinflammatory cytokines, tumor necrosis factor and interleukin-1β, in BDL mice were further elevated by TCDD pretreatment. Liver injury by TCDD plus BDL, such as increased plasma bile acids, bilirubin and aminotransferases, liver necrosis, and increased tumor necrosis factor production, was exaggerated in Cyp1a1/. 1a2(-/-) double knockout mice. These findings indicate that TCDD aggravates cholestatic liver damage and that the presence of CYP1A1 and CYP1A2 plays a protective role in liver damage caused by TCDD and BDL.

Original languageEnglish (US)
Pages (from-to)10-17
Number of pages8
Issue number1-2
StatePublished - Feb 4 2011
Externally publishedYes


  • Aryl hydrocarbon receptor
  • Bile duct ligation
  • Cholestasis
  • Hepatotoxicity
  • TCDD
  • Tumor necrosis factor

ASJC Scopus subject areas

  • Toxicology


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