Fumonisin B 1 exposure and its selective effect on porcine jejunal segment: Sphingolipids, glycolipids and trans-epithelial passage disturbance

Fumonisin B 1 (FB 1) is a mycotoxin produced by Fusarium verticillioides, the cause of Fusarium kernel rot in maize. FB 1 is toxic in domestic and laboratory animals, including pigs. This study investigated the effects of a seven-days-exposure of 1.5 mg/kg b.w. FB 1 on the porcine intestinal epithel...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochemical pharmacology 2007, Vol.74 (1), p.144-152
Hauptverfasser: Loiseau, Nicolas, Debrauwer, Laurent, Sambou, Tounkang, Bouhet, Sandrine, Miller, J. David, Martin, Pascal G., Viadère, Jean-Luc, Pinton, Philippe, Puel, Olivier, Pineau, Thierry, Tulliez, Jacques, Galtier, Pierre, Oswald, Isabelle P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Fumonisin B 1 (FB 1) is a mycotoxin produced by Fusarium verticillioides, the cause of Fusarium kernel rot in maize. FB 1 is toxic in domestic and laboratory animals, including pigs. This study investigated the effects of a seven-days-exposure of 1.5 mg/kg b.w. FB 1 on the porcine intestinal epithelium. Statistically significant increases in the ratio of sphinganine to sphingosine, as well as alterations of the glycolipid distribution were observed in the jejunum. Using a porcine intestinal epithelial cell line (IPEC-1) derived from jejunum and ileum, we tested the effect of FB 1 in vitro in a time- and dose-dependent fashion. A significant increase in sphinganine concentration was observed after 2 days of FB 1 exposure at concentrations >100 μM, or from 6 days of FB 1 exposure at concentration >20 μM. We were also able to show that FB 1 exposure at 200 μM during 16 days increased the intestinal trans-epithelial flux of FB 1. These data indicate that, in pigs, this mycotoxin acts selectively on jejunum cells as follows: (i) FB 1 affects sphingolipid metabolism, as demonstrated by an increase of the amount of free sphingoid bases in a time- and dose-dependent manner, (ii) a depletion of the glycolipids in plasma membranes is observed, and (iii) an increase occurs in the trans-epithelial flux.
ISSN:0006-2952
1873-2968
DOI:10.1016/j.bcp.2007.03.031