The aim of this study was to investigate the interaction of a common polycyclic musk fragrance, namely tonalide (AHTN), with the detoxification gene family CYP1A, by looking at both gene transcription (cyp1a) and enzyme activity (7-ethoxyresorufin-O-deethylase; EROD) in the PLHC-1 fish cell line. Time-dependent (6 and 24 h) exposure experiments with three doses of AHTN (1 nM, 10 nM and 2 μM) were performed. Co-exposure with known CYP1A inducers such as benzo[a]pyrene (B[a]P) and 3,3′-4,4′,5-pentachlorobiphenyl (PCB 126) was also investigated. A slight induction of cyp1a gene transcription was observed after 6 h, but not at 24 h. At 6 h, 40-45% of reduction of cyp1a transcription was observed in co-exposure with B[a]P and PCB 126 compared with single inducers. Complete recovery was observed after 24 h. No effect on EROD activity by AHTN was observed in either single exposure and co-exposure. AHTN seemed not to affect CYP1A at the gene or enzyme level, but in co-exposure with inducers ATHN seems able to reduce detoxification capability within a short time. © 2011 Copyright Taylor and Francis Group, LLC.
DELLA TORRE, C., Biagini, T., Corsi, I., Focardi, S. (2011). Effects on CYP1A of the polycyclic musk tonalide (AHTN) in single and co-exposure with benzo(a)pyrene and 3,3-4,4,5-pentachlorobiphenyl in the PLHC-1 fish cell line. CHEMISTRY IN ECOLOGY, 27(suppl. 2), 57-65 [10.1080/02757540.2011.625935].
Effects on CYP1A of the polycyclic musk tonalide (AHTN) in single and co-exposure with benzo(a)pyrene and 3,3-4,4,5-pentachlorobiphenyl in the PLHC-1 fish cell line
CORSI, I.;FOCARDI, S.
2011-01-01
Abstract
The aim of this study was to investigate the interaction of a common polycyclic musk fragrance, namely tonalide (AHTN), with the detoxification gene family CYP1A, by looking at both gene transcription (cyp1a) and enzyme activity (7-ethoxyresorufin-O-deethylase; EROD) in the PLHC-1 fish cell line. Time-dependent (6 and 24 h) exposure experiments with three doses of AHTN (1 nM, 10 nM and 2 μM) were performed. Co-exposure with known CYP1A inducers such as benzo[a]pyrene (B[a]P) and 3,3′-4,4′,5-pentachlorobiphenyl (PCB 126) was also investigated. A slight induction of cyp1a gene transcription was observed after 6 h, but not at 24 h. At 6 h, 40-45% of reduction of cyp1a transcription was observed in co-exposure with B[a]P and PCB 126 compared with single inducers. Complete recovery was observed after 24 h. No effect on EROD activity by AHTN was observed in either single exposure and co-exposure. AHTN seemed not to affect CYP1A at the gene or enzyme level, but in co-exposure with inducers ATHN seems able to reduce detoxification capability within a short time. © 2011 Copyright Taylor and Francis Group, LLC.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/26053
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