Environmental Nuclear Magnetic Resonance Centre and Department of Physical and Environmental Sciences, University of Toronto Scarborough, Toronto, Ontario, Canada.
Faculty of Science, Ontario Tech University, Oshawa, Ontario, Canada.
Environ Toxicol Chem. 2024 Jun;43(6):1339-1351. doi: 10.1002/etc.5876. Epub 2024 Apr 25.
Pharmaceuticals are found in aquatic environments due to their widespread use and environmental persistence. To date, a range of impairments to aquatic organisms has been reported with exposure to pharmaceuticals; however, further comparisons of their impacts across different species on the molecular level are needed. In the present study, the crustacean Daphnia magna and the freshwater fish Japanese medaka, common model organisms in aquatic toxicity, were exposed for 48 h to the common analgesics acetaminophen (ACT), diclofenac (DCF), and ibuprofen (IBU) at sublethal concentrations. A targeted metabolomic-based approach, using liquid chromatography-tandem mass spectrometry to quantify polar metabolites from individual daphnids and fish was used. Multivariate analyses and metabolite changes identified differences in the metabolite profile for D. magna and medaka, with more metabolic perturbations for D. magna. Pathway analyses uncovered disruptions to pathways associated with protein synthesis and amino acid metabolism with D. magna exposure to all three analgesics. In contrast, medaka exposure resulted in disrupted pathways with DCF only and not ACT and IBU. Overall, the observed perturbations in the biochemistry of both organisms were different and consistent with assessments using other endpoints reporting that D. magna is more sensitive to pollutants than medaka in short-term studies. Our findings demonstrate that molecular-level responses to analgesic exposure can reflect observations of other endpoints, such as immobilization and mortality. Thus, environmental metabolomics can be a valuable tool for selecting sentinel species for the biomonitoring of freshwater ecosystems while also uncovering mechanistic information. Environ Toxicol Chem 2024;43:1339-1351. © 2024 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
由于广泛使用和环境持久性,药品在水生环境中被发现。迄今为止,已有报道称,接触药品会对水生生物造成一系列损害;然而,需要在分子水平上进一步比较它们对不同物种的影响。在本研究中,使用常见的水生毒性模型生物——甲壳类动物大型溞和淡水鱼类日本青鳉,在亚致死浓度下暴露于常见的镇痛药对乙酰氨基酚(ACT)、双氯芬酸(DCF)和布洛芬(IBU)48 小时。使用基于靶向代谢组学的方法,使用液相色谱-串联质谱法从单个大型溞和鱼类中定量测定极性代谢物。多变量分析和代谢物变化确定了大型溞和青鳉的代谢物图谱存在差异,大型溞的代谢紊乱更为严重。途径分析发现,与蛋白质合成和氨基酸代谢相关的途径被扰乱,所有三种镇痛药暴露于大型溞时都会发生这种情况。相比之下,只有 DCF 暴露于青鳉会导致途径紊乱,而 ACT 和 IBU 则不会。总的来说,两种生物体的生物化学观察到的扰动是不同的,这与使用其他终点报告的评估结果一致,即在短期研究中,大型溞比青鳉对污染物更敏感。我们的研究结果表明,对镇痛药暴露的分子水平反应可以反映其他终点(如固定和死亡)的观察结果。因此,环境代谢组学可以成为监测淡水生态系统的生物监测的有价值的工具,同时也揭示了机制信息。Environ Toxicol Chem 2024;43:1339-1351. © 2024 作者。环境毒理化学由 Wiley Periodicals LLC 代表 SETAC 出版。