From mRNA Expression of Drug Disposition Genes to In Vivo Assessment of CYP-Mediated Biotransformation during Zebrafish Embryonic and Larval Development

International Journal of Molecular Sciences

Evy Verbueken¹  Chloé Bars¹  ChrisJ. Van Ginneken¹  StevenJ. Van Cruchten¹  Anna Tochwin²  JonathanS. Ball²  WaleedF. A. Marei³  EllenD. G. Michiels⁴  IsabelleJ. Gabriëls⁴  Jelena Periz-Stanacev⁴  Evelyn Stinckens⁴  Lucia Vergauwen⁴  Dries Knapen⁴ 

[1] Applied Veterinary Morphology, Department of Veterinary Sciences, University of Antwerp, 2610 Wilrijk, Antwerp, Belgium;Biosciences, College of Life and Environmental Sciences, University of Exeter, EX4 4QD Exeter, UK;Gamete Research Centre, Veterinary Physiology and Biochemistry, Department of Veterinary Sciences, University of Antwerp, 2610 Wilrijk, Antwerp, Belgium;Zebrafishlab, Veterinary Physiology and Biochemistry, Department of Veterinary Sciences, University of Antwerp, 2610 Wilrijk, Antwerp, Belgium;

关键词: zebrafish;    embryo;    larva;    development;    cytochrome P450;    phase II;    drug transporter;    biotransformation;    activity;    and expression;   

DOI  :  10.3390/ijms19123976

来源: DOAJ

【 摘 要 】

The zebrafish (Danio rerio) embryo is currently explored as an alternative for developmental toxicity testing. As maternal metabolism is lacking in this model, knowledge of the disposition of xenobiotics during zebrafish organogenesis is pivotal in order to correctly interpret the outcome of teratogenicity assays. Therefore, the aim of this study was to assess cytochrome P450 (CYP) activity in zebrafish embryos and larvae until 14 d post-fertilization (dpf) by using a non-specific CYP substrate, i.e., benzyloxy-methyl-resorufin (BOMR) and a CYP1-specific substrate, i.e., 7-ethoxyresorufin (ER). Moreover, the constitutive mRNA expression of CYP1A, CYP1B1, CYP1C1, CYP1C2, CYP2K6, CYP3A65, CYP3C1, phase II enzymes uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) and sulfotransferase 1st1 (SULT1ST1), and an ATP-binding cassette (ABC) drug transporter, i.e., abcb4, was assessed during zebrafish development until 32 dpf by means of quantitative PCR (qPCR). The present study showed that trancripts and/or the activity of these proteins involved in disposition of xenobiotics are generally low to undetectable before 72 h post-fertilization (hpf), which has to be taken into account in teratogenicity testing. Full capacity appears to be reached by the end of organogenesis (i.e., 120 hpf), although CYP1—except CYP1A—and SULT1ST1 were shown to be already mature in early embryonic development.

【 授权许可】

Unknown