Aquatic Ecology and Toxicology Section, Centre for Organismal Studies, University of Heidelberg, Im Neuenheimer Feld 504, Heidelberg D-69120, Germany.
Environmental Analytical Chemistry, Center for Applied Geosciences, Eberhard Universität Tübingen, Tübingen 72074, Germany.
Environ Sci Technol. 2020 Apr 7;54(7):4200-4209. doi: 10.1021/acs.est.9b07618. Epub 2020 Mar 13.
Fluoxetine has been recognized as one of the most toxic pharmaceuticals in the aquatic environment. Since there is growing evidence that the toxic potential of fluoxetine in surface waters is markedly influenced by its own metabolism in aquatic species, this study investigated the biotransformation of fluoxetine in the zebrafish embryo - an aquatic model organism of intermediate complexity. Zebrafish embryos were exposed to 0.1, 1.0, 10, 50, and 5000 μg/L of fluoxetine from 48 to 120 h post-fertilization (hpf), and the accumulation of fluoxetine and its metabolites was analyzed over time. Additionally, depuration of fluoxetine and its metabolites from 96 to 120 hpf was investigated, and autoinhibitory effects of fluoxetine on phase I biotransformation were analyzed. Exposure to 5000 μg/L fluoxetine resulted in elevated 7-ethoxyresorufin--deethylase (EROD) activity of cytochrome P450 enzymes and continuous accumulation of fluoxetine and 11 fluoxetine metabolites. Embryos exposed to 10 and 50 μg/L fluoxetine were able to reduce fluoxetine accumulation from 94 to 120 hpf. During depuration, accumulation of fluoxetine and most metabolites was clearly reduced, and biotransformation shifted in favor of norfluoxetine, the primary fluoxetine metabolite in humans. Findings demonstrated that norfluoxetine is the only metabolite of fluoxetine that accumulates in zebrafish embryos at environmentally relevant exposure scenarios.
氟西汀已被认为是水生环境中毒性最大的药物之一。由于越来越多的证据表明,氟西汀在地表水中的毒性潜力明显受到其在水生物种中自身代谢的影响,因此本研究调查了氟西汀在斑马鱼胚胎中的生物转化,斑马鱼胚胎是一种具有中等复杂程度的水生模式生物。斑马鱼胚胎从受精后 48 小时到 120 小时(hpf)暴露于 0.1、1.0、10、50 和 5000μg/L 的氟西汀中,并且随着时间的推移分析氟西汀及其代谢物的积累。此外,还研究了从 96 小时到 120 小时氟西汀及其代谢物的排泄情况,并分析了氟西汀对 I 相生物转化的自动抑制作用。暴露于 5000μg/L 的氟西汀导致细胞色素 P450 酶的 7-乙氧基resorufin-O-脱乙基酶(EROD)活性升高和氟西汀及其 11 种代谢物的持续积累。暴露于 10 和 50μg/L 氟西汀的胚胎能够从 94 小时到 120 小时减少氟西汀的积累。在排泄过程中,氟西汀和大多数代谢物的积累明显减少,生物转化向人类中氟西汀的主要代谢物去甲氟西汀倾斜。研究结果表明,去甲氟西汀是在环境相关暴露情况下在斑马鱼胚胎中积累的唯一氟西汀代谢物。