Individual and Combined Effects of Aflatoxin B1 and Sterigmatocystin on Lipid Peroxidation and Glutathione Redox System of Common Carp Liver

Toxins (Basel). 2021 Feb 2;13(2):109. doi: 10.3390/toxins13020109.

Abstract

The purpose of the study was to evaluate the short-term effects of aflatoxin B1 (AFB1 100 µg/kg feed) and sterigmatocystin (STC 1000 μg/kg feed) exposure individually and in combination (100 μg AFB1 + 1000 μg STC/kg feed) on the parameters of lipid peroxidation and glutathione redox system both in biochemical and gene expression levels in one-year-old common carp. Lipid peroxidation parameters were slightly affected, as significant differences were observed only in conjugated diene and triene concentrations. Reduced glutathione content decreased more markedly by STC than AFB1 or AFB1+STC, but glutathione peroxidase activity did not change. Expression of gpx4a, gpx4b, gss, and gsr genes was down-regulated due to STC compared to AFB1 or AFB1+STC, while an induction was found as effect of AFB1+STC in the case of gpx4a, but down-regulation for gpx4b as compared to AFB1. Expression of the glutathione biosynthesis regulatory gene, gss, was higher, but glutathione recycling enzyme encoding gene, gsr, was lower as an effect of AFB1+STC compared to AFB1. These results are supported by the changes in the expression of transcription factors encoding genes, nrf2, and keap1. The results revealed that individual effects of AFB1 and STC on different parameters are synergistic or antagonistic in multi-toxin treatment.

Keywords: aflatoxin B1; common carp; gene expression; glutathione redox system; oxidative stress; sterigmatocystin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aflatoxin B1 / toxicity*
  • Animals
  • Carps / genetics
  • Carps / metabolism*
  • Fish Proteins / genetics
  • Fish Proteins / metabolism
  • Gene Expression Regulation
  • Glutathione / metabolism*
  • Glutathione Reductase / genetics
  • Glutathione Reductase / metabolism
  • Glutathione Synthase / genetics
  • Glutathione Synthase / metabolism
  • Kelch-Like ECH-Associated Protein 1 / genetics
  • Kelch-Like ECH-Associated Protein 1 / metabolism
  • Lipid Peroxidation / drug effects*
  • Liver / drug effects*
  • Liver / metabolism
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / metabolism
  • Oxidation-Reduction
  • Oxidative Stress / drug effects*
  • Phospholipid Hydroperoxide Glutathione Peroxidase / genetics
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism
  • Sterigmatocystin / toxicity*

Substances

  • Fish Proteins
  • Kelch-Like ECH-Associated Protein 1
  • NF-E2-Related Factor 2
  • Sterigmatocystin
  • Aflatoxin B1
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • Glutathione Reductase
  • Glutathione Synthase
  • Glutathione