Gould Sophie L, Winter Matthew J, Trznadel Maciej, Lange Anke, Hamilton Charles M, Boreham Rebekah J, Hetheridge Malcolm J, Young Andrew, Norton William H J, Tyler Charles R
Biosciences, Faculty of Health and Life Sciences, University of Exeter, Stocker Road, Exeter, Devon EX4 4QD, U.K.
Department of Genetics and Genome Biology, College of Life Sciences, University of Leicester, University Rd., Leicester LE1 7RH, U.K.
Environ Sci Technol. 2024 Jul 17;58(30):13194-204. doi: 10.1021/acs.est.3c08126.
Antidepressants are one of the most globally prescribed classes of pharmaceuticals, and drug target conservation across phyla means that nontarget organisms may be at risk from the effects of exposure. Here, we address the knowledge gap for the effects of chronic exposure (28 days) to the tricyclic antidepressant amitriptyline (AMI) on fish, including for concentrations with environmental relevance, using zebrafish () as our experimental model. AMI was found to bioconcentrate in zebrafish, was readily transformed to its major active metabolite nortriptyline, and induced a pharmacological effect (downregulation of the gene encoding the serotonin transporter; ) at environmentally relevant concentrations (0.03 μg/L and above). Exposures to AMI at higher concentrations accelerated the hatch rate and reduced locomotor activity, the latter of which was abolished after a 14 day period of depuration. The lack of any response on the features of physiology and behavior we measured at concentrations found in the environment would indicate that AMI poses a relatively low level of risk to fish populations. The pseudopersistence and likely presence of multiple drugs acting via the same mechanism of action, however, together with a global trend for increased prescription rates, mean that this risk may be underestimated using current ecotoxicological assessment paradigms.
抗抑郁药是全球处方量最大的一类药物,不同门类生物间药物靶点的保守性意味着非靶标生物可能会因接触这些药物而受到影响。在此,我们以斑马鱼()作为实验模型,填补了关于三环类抗抑郁药阿米替林(AMI)对鱼类慢性暴露(28天)影响的知识空白,包括与环境相关浓度的影响。研究发现,AMI可在斑马鱼体内生物富集,很容易转化为其主要活性代谢产物去甲替林,并在与环境相关的浓度(0.03μg/L及以上)下诱导产生药理效应(下调编码5-羟色胺转运体的基因;)。较高浓度的AMI暴露会加快孵化率并降低运动活性,在14天的净化期后,后者的影响消失。在环境中发现的浓度下,我们所测量的生理和行为特征未出现任何反应,这表明AMI对鱼类种群构成的风险相对较低。然而,AMI的假持久性以及可能存在多种通过相同作用机制起作用的药物,再加上全球处方率上升的趋势,意味着使用当前的生态毒理学评估范式可能会低估这种风险。