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Research article - Peer-reviewed, 2004

Comparative cytotoxicity of deoxynivalenol, nivalenol, their acetylated derivatives and de-epoxy metabolites

Eriksen GS, Pettersson H, Lundh T

Abstract

The cytotoxicity of the de-epoxy metabolites of trichothecenes nivalenol (NIV) and deoxynivalenol (DON) was determined and compared with the cytotoxicity of the respective toxin with an intact epoxy group and their acetylated derivatives. The cytotoxic effects was determined by using the 5-bromo-2'-deoxyuridine (BrdU) incorporation assay assessing DNA-synthesis. The toxicity of NIV and DON expressed as the concentration inhibiting 50% of the DNA synthesis (IC50), was occurring at similar micromolar concentrations (1.19 +/- 0.06 and 1.50 +/- 0.34 muM). The toxicity of fusarenon X (4-acetyl NIV) in the assay was similar to the toxicity of NIV, and the toxicity of 15-AcDON was equal to the toxicity of DON. 3-AcDON was less toxic than DON and 15-AcDON. The IC50 value for de-epoxy DON was 54 times higher in the assay than the IC50 for DON, while the IC50 of de-epoxy NIV was 55 times higher than the IC50 for NIV. The results verify previous findings that the de-epoxidation is a detoxification reaction. (C) 2003 Elsevier Ltd. All rights reserved

Keywords

Trichothecene Mycotoxins; Fusarium Mycotoxins; Protein-Synthesis; Cell-Culture; Transformation; Vomitoxin; T-2; Apoptosis; Exposure; Assay

Published in

Food and Chemical Toxicology
2004, volume: 42, number: 4, pages: 619-624
Publisher: PERGAMON-ELSEVIER SCIENCE LTD

Authors' information

Swedish University of Agricultural Sciences, Department of Animal Nutrition and Management
Pettersson, Hans
Swedish University of Agricultural Sciences, Department of Animal Nutrition and Management
Eriksen, Gunnar S
Swedish University of Agricultural Sciences, Department of Animal Nutrition and Management

UKÄ Subject classification

Veterinary Science
Animal and Dairy Science
Food Science

Publication Identifiers

DOI: https://doi.org/10.1016/j.fct.2003.11.006

URI (permanent link to this page)

https://res.slu.se/id/publ/3321