Toxicity and cytochrome P450 1A mRNA induction by 6-formylindolo[3,2-b]carbazole (FICZ) in chicken and Japanese quail embryos

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• 作者：Maria E. Jö ; nsson ; ^{maria.jonsson@ebc.uu.se" class="auth_mail" title="E-mail the corresponding author} ; Anna Mattsson ; Siraz Shaik¹ ; Bjö ; rn Brunströ ; m
• 关键词：AHR ; aryl hydrocarbon receptor ; CYP ; cytochrome P450 ; CYP1 ; cytochrome P450 family 1 ; E ; PCR efficiency ; EROD ; 7-ethoxyresorufin-O-deethylase ; FICZ ; formylindolo[3 ; 2-b]carbazole ; KCZ ; ketoconazole ; PCBs ; polychlorinated biphenyls ; PCB126 ; 3 ; 3&prime ; 4 ; 4&prime ; 5-pentachlorobiphenyl ; qPCR ; quantitative real time RT-PCR ; TCDD ; 2 ; 3 ; 7 ; 8-tetrachlorodibenzo-p-dioxin
• 刊名：Comparative Biochemistry and Physiology, Part C
• 出版年：2016
• 出版时间：January 2016
• 年：2016
• 卷：179
• 期：Complete
• 页码：125-136
• 全文大小：1984 K

文摘

The tryptophan derivative formylindolo[3,2-b]carbazole (FICZ) binds with high ligand affinity to the aryl hydrocarbon receptor (AHR) and is readily degraded by AHR-regulated cytochrome P450 family 1 (CYP1) enzymes. Whether in vivo exposure to FICZ can result in toxic effects has not been examined and the main objective of this study was to determine if FICZ is embryotoxic in birds. We examined toxicity and CYP1 mRNA induction of FICZ in embryos from chicken (Gallus domesticus) and Japanese quail (Coturnix japonica) exposed to FICZ (2–200 μg kg^− 1) by yolk and air sac injections. FICZ caused liver toxicity, embryo mortality, and CYP1A4 and CYP1A5 induction in both species with similar potency. This is in stark contrast to the very large difference in sensitivity of these species to halogenated AHR agonists. We also exposed chicken embryos to a low dose of FICZ (4 μg kg^− 1) in combination with a CYP inhibitor, ketoconazole (KCZ). The mixture of FICZ and KCZ was lethal while FICZ alone had no effect at 4 μg kg^− 1. Furthermore, mixed exposure to FICZ and KCZ caused stronger and more long-lasting hepatic CYP1A4 induction than exposure to each compound alone. These findings indicate reduced biotransformation of FICZ by co-treatment with KCZ as a cause for the enhanced effects although additive AHR activation is also possible. To conclude, FICZ is toxic to bird embryos and it seems reasonable that the toxicity by FICZ involves AHR activation. However, the molecular targets and biological events leading to hepatic damage and mortality are unknown.