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Selective impairment of drug-metabolizing enzymes in pig liver during subchronic dietary exposure to aflatoxin B1.
Authors:Guylaine M Meissonnier  Joelle Laffitte  Nicolas Loiseau  Etienne Benoit  Isabelle Raymond  Philippe Pinton  Anne-Marie Cossalter  Gérard Bertin  Isabelle P Oswald  Pierre Galtier
Institution:Laboratoire de Pharmacologie-Toxicologie UR66, INRA, F-31931 Toulouse Cedex 9, France.
Abstract:Consequences of subchronic exposure to aflatoxin B1 (AFB1) on liver monooxygenase and transferase enzymes were compared in control pigs and pigs given 385, 867 or 1,807 microg AFB1/kg of feed for 4 weeks. Animals exposed to the highest dose of toxin developed clinical signs of aflatoxicosis, like liver fibrosis, hepatic dysfunction and decreased weight gain. This group had significantly lower levels of liver cytochrome P450, ethoxyresorufin O-deethylase (EROD) activity, testosterone metabolism, P450 1A and P450 3A protein expression. By comparison, mild degenerative hepatic changes, no hepatic dysfunction but a similar pattern of liver P450 enzymes activity without changes in P450 3A expression were observed in pigs exposed to 867 microg AFB1/kg of feed. Benzphetamine and aminopyrine N-demethylase activities were increased in pigs exposed to 867 or 1,807microg AFB1/kg of feed. Pigs exposed to 385 microg AFB1/kg of feed had low levels of EROD activity and all other biotransformation and clinical parameters remained at control levels. Aniline hydroxylase activity, P450 2C protein expression, UDP-glucuronosyl and glutathione S-transferase activities were unaffected at all doses of AFB1. In conclusion, P450 1A and P450 3A appear to be specific targets of AFB1 even if pig did not display clinical sign of liver toxicosis.
Keywords:AFB1  aflatoxin B1  ALP  alkaline phosphatase  AST  aspartate transaminase  ALT  alanine transaminase  CDNB  1-chloro-2  4-dinitrobenzene  EROD  ethoxyresorufin O-deethylase  GST  glutathione S-transferase  γ-GT  γ-glutamyl transpeptidase  H&  E  haematoxylin and eosin  PAS  periodic acid-Schiff reagent  PNP  p-nitrophenol  P450  cytochrome P450  SDS–PAGE  sodium dodecyl sulfate–polyacrylamide gel electrophoresis  UGT  UDP-glucuronosyl transferase
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