| Literature DB >> 31834428 |
Amelie Catteuw1, Mathias Devreese1, Siegrid De Baere1, Gunther Antonissen1,2, Lada Ivanova3, Silvio Uhlig3, Ann Martens4, Sarah De Saeger5, Marthe De Boevre5, Siska Croubels6.
Abstract
Age-related differences in toxicokinetic processes of deoxynivalenol (DON) and deoxynivalenol-3-glucoside (DON3G) were studied. DON3G [55.7 µg/kg bodyweight (BW)] and an equimolar dose of DON (36 µg/kg BW) were administered to weaned piglets (4 weeks old) by single intravenous and oral administration in a double two-way cross-over design. Systemic and portal blood was sampled at different time points pre- and post-administration and plasma concentrations of DON, DON3G and their metabolites were quantified using validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) and liquid chromatography-high-resolution mass spectrometry (LC-HRMS) methods. Data were processed using tailor-made compartmental toxicokinetic (TK) models to accurately estimate TK parameters. Results were statistically compared to data obtained in a previous study on 11-week-old pigs using identical experimental conditions. Significant age-related differences in intestinal and systemic exposure to both DON and DON3G were noted. Most remarkably, a significant difference was found for the absorbed fraction of DON3G, after presystemic hydrolysis to DON, in weaned piglets compared to 11-week-old piglets (83% vs 16%, respectively), assumed to be mainly attributed to the higher intestinal permeability of weaned piglets. Other differences in TK parameters could be assigned to a higher water/fat body ratio and longer gastrointestinal transit time of weaned piglets. Results may further refine current risk assessment concerning DON and DON3G in animals. Additionally, since piglets possibly serve as a human paediatric surrogate model, results may be extrapolated to human infants.Entities:
Keywords: Deoxynivalenol; Deoxynivalenol-3-glucoside; Pig; Plasma protein binding; Toxicokinetics; Weaning
Mesh:
Substances:
Year: 2019 PMID: 31834428 DOI: 10.1007/s00204-019-02644-x
Source DB: PubMed Journal: Arch Toxicol ISSN: 0340-5761 Impact factor: 5.153