Nivalenol Has a Greater Impact than Deoxynivalenol on Pig Jejunum Mucosa in Vitro on Explants and in Vivo on Intestinal Loops

• Published in: Toxins Vol. 7; no. 6; pp. 1945 - 1961
• Main Authors: Cheat, Sophal, Gerez, Juliana, Cognié, Juliette, Alassane-Kpembi, Imourana, Bracarense, Ana, Raymond-Letron, Isabelle, Oswald, Isabelle, Kolf-Clauw, Martine
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 29.05.2015; MDPI
• Subjects: Animals; Apoptosis - drug effects; Cell Proliferation - drug effects; Contaminants; deoxynivalenol; enterocytes; Enterocytes - drug effects; Enterocytes - pathology; Female; Food contamination; histomorphology; In Vitro Techniques; Ingestion; Intestinal Mucosa - drug effects; Intestinal Mucosa - pathology; Jejunum - drug effects; Jejunum - pathology; jejunum explant; Life Sciences; loops; Mycotoxins; nivalenol; Other; Reproducibility of Results; Risk assessment; Swine; Toxicology; Trichothecenes - toxicity; deoxynivalenol; mycotoxins; nivalenol; jejunum explant; loops; enterocytes; histomorphology; intestine; porcin; animal modèle; pig; santé publique; intestinal disease; pathologie intestinale; animal model; intestin; public health
• ISSN: 2072-6651; 2072-6651
• DOI: 10.3390/toxins7061945

The mycotoxins deoxynivalenol (DON) and nivalenol (NIV), worldwide cereal contaminants, raise concerns for animal and human gut health, following contaminated food or feed ingestion. The impact of DON and NIV on intestinal mucosa was investigated after acute exposure, in vitro and in vivo. The histological changes induced by DON and NIV were analyzed after four-hour exposure on pig jejunum explants and loops, two alternative models. On explants, dose-dependent increases in the histological changes were induced by DON and NIV, with a two-fold increase in lesion severity at 10 µM NIV. On loops, NIV had a greater impact on the mucosa than DON. The overall proliferative cells showed 30% and 13% decrease after NIV and DON exposure, respectively, and NIV increased the proliferative index of crypt enterocytes. NIV also increased apoptosis at the top of villi and reduced by almost half the proliferative/apoptotic cell ratio. Lamina propria cells (mainly immune cells) were more sensitive than enterocytes (epithelial cells) to apoptosis induced by NIV. Our results demonstrate a greater impact of NIV than DON on the intestinal mucosa, both in vitro and in vivo, and highlight the need of a specific hazard characterization for NIV risk assessment.