Toxic effects of dietary exposure to T-2 toxin on intestinal and hepatic biotransformation enzymes and drug transporter systems in broiler chickens. 2013

A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
Department of Pharmacology, Toxicology and Biochemistry, Faculty of Veterinary Medicine, Ghent University, Belgium. ann.osselaere@ugent.be

The effects of the mycotoxin T-2 on hepatic and intestinal drug-metabolizing enzymes (cytochrome P450) and drug transporter systems (MDR1 and MRP2) in poultry were investigated during this study. Broiler chickens received either uncontaminated feed, feed contaminated with 68μg/kg or 752μg/kg T-2 toxin. After 3weeks, the animals were euthanized and MDR1, MRP2, CYP1A4, CYP1A5 and CYP3A37 mRNA expression were analyzed using qRT-PCR. Along the entire length of the small intestine no significant differences were observed. In the liver, genes coding for CYP1A4, CYP1A5 and CYP3A37 were significantly down-regulated in the group exposed to 752μg/kg T-2. For CYP1A4, even a contamination level of 68μg/kg T-2 caused a significant decrease in mRNA expression. Expression of MDR1 was not significantly decreased in the liver. In contrast, hepatic MRP2 expression was significantly down-regulated after exposure to 752μg/kg T-2. Hepatic and intestinal microsomes were prepared to test the enzymatic activity of CYP3A. In the ileum and liver CYP3A activity was significantly increased in the group receiving 752μg/kg T-2 compared to the control group. The results of this study show that drug metabolizing enzymes and drug transporter mechanisms can be influenced due to prolonged exposure to relevant doses of T-2.

UI MeSH Term Description Entries
D007413 Intestinal Mucosa Lining of the INTESTINES, consisting of an inner EPITHELIUM, a middle LAMINA PROPRIA, and an outer MUSCULARIS MUCOSAE. In the SMALL INTESTINE, the mucosa is characterized by a series of folds and abundance of absorptive cells (ENTEROCYTES) with MICROVILLI. Intestinal Epithelium,Intestinal Glands,Epithelium, Intestinal,Gland, Intestinal,Glands, Intestinal,Intestinal Gland,Mucosa, Intestinal
D007422 Intestines The section of the alimentary canal from the STOMACH to the ANAL CANAL. It includes the LARGE INTESTINE and SMALL INTESTINE. Intestine
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D001835 Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. Body Weights,Weight, Body,Weights, Body
D002645 Chickens Common name for the species Gallus gallus, the domestic fowl, in the family Phasianidae, order GALLIFORMES. It is descended from the red jungle fowl of SOUTHEAST ASIA. Gallus gallus,Gallus domesticus,Gallus gallus domesticus,Chicken
D003577 Cytochrome P-450 Enzyme System A superfamily of hundreds of closely related HEMEPROTEINS found throughout the phylogenetic spectrum, from animals, plants, fungi, to bacteria. They include numerous complex monooxygenases (MIXED FUNCTION OXYGENASES). In animals, these P-450 enzymes serve two major functions: (1) biosynthesis of steroids, fatty acids, and bile acids; (2) metabolism of endogenous and a wide variety of exogenous substrates, such as toxins and drugs (BIOTRANSFORMATION). They are classified, according to their sequence similarities rather than functions, into CYP gene families (>40% homology) and subfamilies (>59% homology). For example, enzymes from the CYP1, CYP2, and CYP3 gene families are responsible for most drug metabolism. Cytochrome P-450,Cytochrome P-450 Enzyme,Cytochrome P-450-Dependent Monooxygenase,P-450 Enzyme,P450 Enzyme,CYP450 Family,CYP450 Superfamily,Cytochrome P-450 Enzymes,Cytochrome P-450 Families,Cytochrome P-450 Monooxygenase,Cytochrome P-450 Oxygenase,Cytochrome P-450 Superfamily,Cytochrome P450,Cytochrome P450 Superfamily,Cytochrome p450 Families,P-450 Enzymes,P450 Enzymes,Cytochrome P 450,Cytochrome P 450 Dependent Monooxygenase,Cytochrome P 450 Enzyme,Cytochrome P 450 Enzyme System,Cytochrome P 450 Enzymes,Cytochrome P 450 Families,Cytochrome P 450 Monooxygenase,Cytochrome P 450 Oxygenase,Cytochrome P 450 Superfamily,Enzyme, Cytochrome P-450,Enzyme, P-450,Enzyme, P450,Enzymes, Cytochrome P-450,Enzymes, P-450,Enzymes, P450,Monooxygenase, Cytochrome P-450,Monooxygenase, Cytochrome P-450-Dependent,P 450 Enzyme,P 450 Enzymes,P-450 Enzyme, Cytochrome,P-450 Enzymes, Cytochrome,Superfamily, CYP450,Superfamily, Cytochrome P-450,Superfamily, Cytochrome P450
D004032 Diet Regular course of eating and drinking adopted by a person or animal. Diets
D000097202 ATP-Binding Cassette Sub-Family B Member 4 An ATP-binding cassette, sub-family B protein that functions in translocating PHOSPHATIDYLCHOLINES from the inner to the outer leaflet of the canalicular membrane of the HEPATOCYTES. MDR2 Protein,Multidrug Resistance Protein 2,P-Glycoprotein 2,Pgp2 protein,Phosphatidylcholine Translocator ABCB4,2, P-Glycoprotein,ABCB4, Phosphatidylcholine Translocator,ATP Binding Cassette Sub Family B Member 4,P Glycoprotein 2,Translocator ABCB4, Phosphatidylcholine,protein, Pgp2
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA

Related Publications

A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
October 1988, Poultry science,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
September 1973, Poultry science,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
December 2000, Food additives and contaminants,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
January 1983, National Institute of Animal Health quarterly,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
January 2016, Journal of agricultural and food chemistry,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
September 2009, Environmental toxicology and pharmacology,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
June 2016, Journal of animal physiology and animal nutrition,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
June 2007, Poultry science,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
August 2014, Journal of veterinary pharmacology and therapeutics,
A Osselaere, and S J Li, and L De Bock, and M Devreese, and J Goossens, and V Vandenbroucke, and J Van Bocxlaer, and K Boussery, and F Pasmans, and A Martel, and P De Backer, and S Croubels
April 1983, Canadian journal of comparative medicine : Revue canadienne de medecine comparee,
Copied contents to your clipboard!