4.7 Article

Tissue distribution and proinflammatory cytokine gene expression following acute oral exposure to deoxynivalenol: Comparison of weanling and adult mice

Journal

FOOD AND CHEMICAL TOXICOLOGY
Volume 46, Issue 8, Pages 2826-2831

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2008.05.016

Keywords

deoxynivalenol; trichothecene; mycotoxin; age; toxicokinetics; cytokine

Funding

  1. NIDDK NIH HHS [R01 DK058833, R01 DK058833-07] Funding Source: Medline
  2. NIEHS NIH HHS [R56 ES003358, ES 3358, R01 ES003358-22, R01 ES003358] Funding Source: Medline

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The frequent presence of deoxynivalenol (DON) in cereal-based foods and the high intake of these foods by children raises particular concerns about the relative susceptibility of this subpopulation to adverse effects evoked by this mycotoxin. We tested the hypothesis that both toxicokinetics and proinflammatory cytokine gene expression following a oral DON exposure at 5 mg/kg bw differ between weanling (34 wk) and young adult (8-10 wk) female mice. DON was rapidly taken up with maximum plasma concentrations reaching 1.0 mu g/ml in adult mice at 15 min, whereas DON levels were approximately twice as much in weanling mice at these times. DON was rapidly cleared in both weanling and adult mice with concentrations being reduced by 78% and 81% of the peak levels, respectively, after 2 h. DON accumulation and clearance in spleen, liver, lung and kidney followed similar kinetics to that of plasma with tissue burdens also reaching twice that of adult Mice. When TNF-alpha, IL-1 beta and IL-6 mRNAs in spleens (a primary source of systemic proinflammatory cytokines) were used as biomarkers of the DON's effects, expression of these mRNAs was two to three times greater in weanling than adult mouse. However, differences in proinflammatory cytokine expression were less robust or not apparent in the liver or lung. Taken together, these data suggest that young mice are modestly more susceptible than adult mice to the adverse effects of DON and that this might result from a greater toxin tissue burden. (c) 2008 Elsevier Ltd. All rights reserved.

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