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

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 b...

Full description

Saved in:
Bibliographic Details
Published inToxins Vol. 13; no. 2; p. 109
Main Authors Kövesi, Benjamin, Kulcsár, Szabina, Ancsin, Zsolt, Zándoki, Erika, Erdélyi, Márta, Mézes, Miklós, Balogh, Krisztián
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 02.02.2021
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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 and 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 but down-regulation for as compared to AFB1. Expression of the glutathione biosynthesis regulatory gene, , was higher, but glutathione recycling enzyme encoding gene, 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, and The results revealed that individual effects of AFB1 and STC on different parameters are synergistic or antagonistic in multi-toxin treatment.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2072-6651
2072-6651
DOI:10.3390/TOXINS13020109