Omics-based identification of the combined effects of idiosyncratic drugs and inflammatory cytokines on the development of drug-induced liver injury

Toxicol Appl Pharmacol. 2017 Oct 1:332:100-108. doi: 10.1016/j.taap.2017.07.014. Epub 2017 Jul 18.

Abstract

The mechanisms of idiosyncratic drug-induced hepatotoxicity remain largely unclear. It has demonstrated that the drug idiosyncrasy is potentiated in the context of inflammation and intracellular ceramides may play a role in this process. To study the mechanisms, HepG2 cells were co-treated with high and low doses of three idiosyncratic (I) and three non-idiosyncratic (N) compounds, with (I+ and N+) or without (I- and N-) a cytokine mix. Microarray, lipidomics and flow cytometry were performed to investigate the genome-wide expression patterns, the intracellular ceramide levels and the induction of apoptosis. We found that all I+ treatments significantly influenced the immune response- and response to stimulus-associated gene ontology (GO) terms, but the induction of apoptotic pathways, which was confirmed by flow cytometry, only appeared to be induced after the high-dose treatment. The ceramide signaling-, ER stress-, NF-kB activation- and mitochondrial activity-related pathways were biologically involved in apoptosis induced by the high-dose I+. Additionally, genes participating in ceramide metabolism were significantly altered resulting in a measurable increase in ceramide levels. The increases in ceramide concentrations may induce ER stress and activate the JNK pathway by affecting the expression of the related genes, and eventually trigger the mitochondria-independent apoptosis in hepatocytes. Overall, our study provides a potential mechanism to explain the role of inflammation in idiosyncratic drug reactions.

Keywords: Apoptosis; Ceramide; Drug-induced liver injury; ER stress; Microarray; Toxicogenomics.

MeSH terms

  • Apoptosis / drug effects
  • Ceramides / metabolism
  • Chemical and Drug Induced Liver Injury / metabolism*
  • Cytokines / metabolism*
  • Dose-Response Relationship, Drug
  • Endoplasmic Reticulum Stress / drug effects
  • Gene Expression Profiling
  • Hep G2 Cells
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Humans
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism
  • MAP Kinase Signaling System
  • Metabolomics
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Signal Transduction
  • Tandem Mass Spectrometry

Substances

  • Ceramides
  • Cytokines
  • NF-kappa B