Glutathione S-transferase A1 (GSTA1) as a marker of acetaminophen-induced hepatocyte injury in vitro

Toxicol Mech Methods. 2017 Jul;27(6):401-407. doi: 10.1080/15376516.2017.1320457. Epub 2017 May 2.

Abstract

Acetaminophen (APAP) overdose causes serious hepatocyte injury, and new markers are needed to predict APAP-induced hepatic injury. Glutathione S-transferase A1 (GSTA1) plays a significant role in the metabolism of APAP. Primary mouse hepatocytes were isolated by a two-step perfusion in situ. An APAP-induced hepatocyte injury model was used to characterize GSTA1 in APAP treated cells and determine whether GSTA1 could be a prognostic marker in vitro. A significant increase (p < .05) in GSTA1 in cell culture supernatant was detected at 6 h after APAP treatment, while alanine aminotransferase (ALT), aspartate aminotransferase (AST), malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione (GSH) showed marked differences (p < .05) at 8 h after APAP exposure, 2 h later than GSTA1. Furthermore, GSTA1 increased in a dose-dependent manner with APAP treatment. GSTA1 increased significantly (p < .05) at a concentration of 5.0 mmol/L APAP, while the marked changes in ALT, AST and other indexes were undetectable until the concentration of APAP reached 7.5 mmol/L. These results suggest that increased GSTA1 can be more sensitive than ALT and other indexes as a marker of APAP-induced hepatic injury, which provide novel diagnostic index for APAP-induced hepatic injury and supply valuable information to further understand the pathogenesis of liver damage.

Keywords: APAP; GSTA1; hepatocytes injury; in vitro; marker.

MeSH terms

  • Acetaminophen / metabolism
  • Acetaminophen / toxicity*
  • Animals
  • Biomarkers / metabolism
  • Cells, Cultured
  • Chemical and Drug Induced Liver Injury / enzymology*
  • Chemical and Drug Induced Liver Injury / etiology
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Glutathione Transferase / metabolism*
  • Hepatocytes / drug effects*
  • Hepatocytes / enzymology
  • Isoenzymes / metabolism*
  • Male
  • Mice, Inbred Strains
  • Primary Cell Culture
  • Time Factors

Substances

  • Biomarkers
  • Isoenzymes
  • Acetaminophen
  • Glutathione Transferase
  • glutathione S-transferase alpha