Effects of chronic exposure to tributyltin on tissue-specific cytochrome P450 1 regulation in juvenile common carp
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- Klíčová slova
- CYP450 1 family genes, EROD, fish, tissue-specific response, tributyltin,
- MeSH
- cytochrom P-450 CYP1A1 metabolismus MeSH
- kapři genetika MeSH
- lineární modely MeSH
- messenger RNA genetika metabolismus MeSH
- orgánová specificita účinky léků MeSH
- regulace genové exprese enzymů účinky léků MeSH
- systém (enzymů) cytochromů P-450 genetika metabolismus MeSH
- trialkylcínové sloučeniny toxicita MeSH
- vystavení vlivu životního prostředí * MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cytochrom P-450 CYP1A1 MeSH
- messenger RNA MeSH
- systém (enzymů) cytochromů P-450 MeSH
- trialkylcínové sloučeniny MeSH
- tributyltin MeSH Prohlížeč
1. The purpose of this study was to compare tributyltin (TBT)-induced cytochrome P450 1 (CYP450 1) regulation in liver, gills and muscle of juvenile common carp (Cyprinus carpio). 2. Fish were exposed to sublethal concentrations of TBT (75, 0.75 and 7.5 μg/L) for 60 days. CYP450 1A was measured at the enzyme activity level as 7-ethoxyresorufin-O-deethylase (EROD) activity, as well as the mRNA expression of CYP450 1 family genes (CYP1A, CYP1B, CYP1C1 and CYP1C2) in fish tissues. 3. Based on the results, the liver displayed the highest absolute levels of EROD activity, both under nonexposed and exposed conditions. Additional, EROD activities and CYP1A gene levels showed a good correlation in all three organs. According to the mRNA expression of CYP450 1 family genes, it suggested that CYP1A was to accommodate most EROD activity in fish, but other CYP450 forms also involved in this proceeding. 4. Overall, the study revealed both similarities and differences in the concentration-dependent CYP450 1 responses of the three target organs, which could provide useful information to better understand the mechanisms of TBT-induced bio-toxicity.
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