Fumonisin B1 Induces Oxidative Stress and Breaks Barrier Functions in Pig Iliac Endothelium Cells

Toxins (Basel). 2019 Jul 2;11(7):387. doi: 10.3390/toxins11070387.

Abstract

Fumonisins (Fums) are types of mycotoxin that widely contaminante feed material crops, and can trigger potential biological toxicities to humans and various animals. However, the toxicity of Fums on porcine blood vessels has not been fully explored. Fumonisin B1 (FB1) is the main component of Fums. Therefore, the aim of this study was to explore the effects of FB1 on the oxidative stress and tight junctions of the pig iliac endothelial cells (PIECs) in vitro. The results showed that FB1 reduced the viability of PIECs, increased the contents of lipid peroxidation product malondialdehyde (MDA), decreased the activities of antioxidant enzymes superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and thioredoxin reductase (TrxR), and decreased the level of glutathione (GSH). In addition, the barrier functions were destroyed, along with the down-regulations on Claudin 1, Occludin and ZO-1 and the increase of paracellular permeability. Thus, this research indicates that FB1 facilitates oxidative stress and breaks barrier functions to damage pig iliac endothelium cells.

Keywords: Fumonisin B1; oxidative stress; pig iliac endothelial cells; tight junction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catalase / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Endothelial Cells / drug effects*
  • Endothelial Cells / metabolism
  • Endothelium, Vascular / cytology
  • Fumonisins / toxicity*
  • Glutathione / metabolism
  • Glutathione Peroxidase / metabolism
  • Iliac Artery / cytology*
  • Lipid Peroxidation / drug effects
  • Malondialdehyde / metabolism
  • Oxidative Stress / drug effects*
  • Permeability / drug effects
  • Superoxide Dismutase / metabolism
  • Swine
  • Tight Junctions / metabolism

Substances

  • Fumonisins
  • fumonisin B1
  • Malondialdehyde
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione