Deoxynivalenol impairs hepatic and intestinal gene expression of selected oxidative stress, tight junction and inflammation proteins in broiler chickens, but addition of an adsorbing agent shifts the effects to the distal parts of the small intestine

PLoS One. 2013 Jul 26;8(7):e69014. doi: 10.1371/journal.pone.0069014. Print 2013.

Abstract

Broiler chickens are rather resistant to deoxynivalenol and thus, clinical signs are rarely seen. However, effects of subclinical concentrations of deoxynivalenol on both the intestine and the liver are less frequently studied at the molecular level. During our study, we investigated the effects of three weeks of feeding deoxynivalenol on the gut wall morphology, intestinal barrier function and inflammation in broiler chickens. In addition, oxidative stress was evaluated in both the liver and intestine. Besides, the effect of a clay-based mycotoxin adsorbing agent on these different aspects was also studied. Our results show that feeding deoxynivalenol affects the gut wall morphology both in duodenum and jejenum of broiler chickens. A qRT-PCR analysis revealed that deoxynivalenol acts in a very specific way on the intestinal barrier, since only an up-regulation in mRNA expression of claudin 5 in jejunum was observed, while no effects were seen on claudin 1, zona occludens 1 and 2. Addition of an adsorbing agent resulted in an up-regulation of all the investigated genes coding for the intestinal barrier in the ileum. Up-regulation of Toll-like receptor 4 and two markers of oxidative stress (heme-oxigenase or HMOX and xanthine oxidoreductase or XOR) were mainly seen in the jejunum and to a lesser extent in the ileum in response to deoxynivalenol, while in combination with an adsorbing agent main effect was seen in the ileum. These results suggest that an adsorbing agent may lead to higher concentrations of deoxynivalenol in the more distal parts of the small intestine. In the liver, XOR was up-regulated due to DON exposure. HMOX and HIF-1α (hypoxia-inducible factor 1α) were down-regulated due to feeding DON but also due to feeding the adsorbing agent alone or in combination with DON.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Animals
  • Biomarkers / metabolism
  • Chickens / genetics
  • Gene Expression Regulation / drug effects*
  • Genes, Essential
  • Ileum / drug effects
  • Ileum / metabolism
  • Ileum / pathology
  • Inflammation / genetics*
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism*
  • Intestine, Small / pathology
  • Jejunum / drug effects
  • Jejunum / metabolism
  • Jejunum / pathology
  • Liver / metabolism*
  • Liver / pathology
  • Oxidative Stress / drug effects
  • Oxidative Stress / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tight Junctions / drug effects
  • Tight Junctions / metabolism*
  • Trichothecenes / toxicity*

Substances

  • Biomarkers
  • RNA, Messenger
  • Trichothecenes
  • deoxynivalenol

Grants and funding

This work was supported by the BOF-project 01J08309 from Ghent University. There were no additional external funding sources for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.