Interaction of tributyltin with hepatic cytochrome P450 and uridine diphosphate-glucuronosyl transferase systems of fish: In vitro studies

• Published in: Environmental toxicology and chemistry 2004-04, Vol.23 (4), p.990-996
• Main Authors: Morcillo, Yolanda, Janer, Gemma, O'Hara, Sean C.M., Livingstone, David R., Porte, Cinta
• Format: Article
• Language: English
• Subjects: Agnatha. Pisces; Animal, plant and microbial ecology; Animals; Applied ecology; Benthic fish; Benzo[a]pyrene metabolism; Biological and medical sciences; Cytochrome P-450 CYP1A1 - pharmacology; Cytochrome P-450 Enzyme System - pharmacology; Ecotoxicology, biological effects of pollution; Effects of pollution and side effects of pesticides on vertebrates; Flounder - physiology; Fundamental and applied biological sciences. Psychology; General aspects; Glucuronosyltransferase - pharmacology; Microsomes, Liver - enzymology; Mullus barbatus; Platichthys flesus; Smegmamorpha - physiology; Testosterone - pharmacology; Trialkyltin Compounds - toxicity; Tributyltin; Uridine Diphosphate - pharmacology; Uridine diphosphate-glucuronyl transferase
• ISSN: 0730-7268; 1552-8618
• DOI: 10.1897/034-262

Hepatic microsomes of red mullet (Mullus barbatus) and flounder (Platichthys flesus) were preincubated in the presence of a concentration range of the antifouling agent tributyltin (TBT) chloride, and the interactions of TBT with cytochrome P450 and uridine diphosphate—glucuronyl transferase systems were investigated. The enzyme systems were examined in terms of cytochrome P4501A (CYP1A)‐catalyzed 7‐ethoxyresorufin O‐deethylase (EROD) activity and benzo[a]pyrene (BaP) metabolism and in terms of glucuronidation of testosterone and 17β‐estradiol, respectively. Ethoxyresorufin O‐deethylase and BaP hydroxylase (BPH) activities of both fish species were progressively inhibited by increasing concentrations of TBT, and the effects were more pronounced for EROD than for BPH (maximal inhibition at 100 μM TBT for EROD and 250–500 μM TBT for BPH). Hydroxylated metabolites of BaP (3‐hydroxy‐, 7,8‐dihydrodiol, and 9,10‐dihydrodiol), representing 95% of the total metabolites formed, were reduced up to 75 % in the presence of 100 to 500 μM TBT, whereas the formation of other metabolites was less affected. This may alter BaP toxicity and carcinogenicity. Overall, the results were consistent with a specific inhibitory effect of TBT on CYP1A in the two fish species. Additionally, the conjugation of testosterone was significantly inhibited (20%) at low TBT doses (5 μM), with no effect on the glucuronidation of estradiol.