Hepatocyte-Specific Deficiency of DAX-1 Protects Mice from Acetaminophen-Induced Hepatotoxicity by Activating NRF2 Signaling

Int J Mol Sci. 2022 Oct 4;23(19):11786. doi: 10.3390/ijms231911786.

Abstract

Acetaminophen (APAP) is a widely used analgesic and antipyretic drug, but its overdose can cause acute liver failure. The dosage-sensitive sex reversal adrenal hypoplasia congenita critical region on the X chromosome, gene 1 (DAX-1, NR0B1), is an orphan nuclear receptor that acts as a transcriptional co-repressor of various genes. In this study, we identified the role of DAX-1 in APAP-induced liver injury using hepatocyte-specific Dax-1 knockout (Dax-1 LKO) mice. Mouse primary hepatocytes were used as a comparative in vitro study. APAP overdose led to decreased plasma alanine aminotransferase and aspartate aminotransferase levels in Dax-1 LKO mice compared to C57BL/6J (WT) controls, accompanied by reduced liver necrosis. The expression of the genes encoding the enzymes catalyzing glutathione (GSH) synthesis and metabolism and antioxidant enzymes was increased in the livers of APAP-treated Dax-1 LKO mice. The rapid recovery of GSH levels in the mitochondrial fraction of APAP-treated Dax-1 LKO mice led to reduced reactive oxygen species levels, resulting in the inhibition of the prolonged JNK activation. The hepatocyte-specific DAX-1 deficiency increased the protein expression of nuclear factor erythroid 2-related factor 2 (Nrf2) compared with WT controls after APAP administration. These results indicate that DAX-1 deficiency in hepatocytes protects against APAP-induced liver injury by Nrf2-regulated antioxidant defense.

Keywords: DAX-1; Nrf2; acetaminophen; hepatotoxicity.

MeSH terms

  • Acetaminophen / toxicity
  • Alanine Transaminase / metabolism
  • Animals
  • Antioxidants / metabolism
  • Antipyretics*
  • Aspartate Aminotransferases / metabolism
  • Chemical and Drug Induced Liver Injury* / genetics
  • Chemical and Drug Induced Liver Injury* / metabolism
  • Chemical and Drug Induced Liver Injury* / prevention & control
  • Co-Repressor Proteins / metabolism
  • DAX-1 Orphan Nuclear Receptor* / genetics
  • Glutathione / metabolism
  • Hepatocytes / metabolism
  • Liver / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NF-E2-Related Factor 2* / genetics
  • NF-E2-Related Factor 2* / metabolism
  • Orphan Nuclear Receptors / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Antioxidants
  • Antipyretics
  • Co-Repressor Proteins
  • DAX-1 Orphan Nuclear Receptor
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Orphan Nuclear Receptors
  • Reactive Oxygen Species
  • Acetaminophen
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Glutathione