D'Iglio Claudio, Famulari Sergio, Capparucci Fabiano, Gervasi Claudio, Cuzzocrea Salvatore, Spanò Nunziacarla, Di Paola Davide
Department of Chemical, Biological, Pharmaceutical, and Environmental Science, University of Messina, 98166 Messina, Italy.
Department of Pharmacological and Physiological Science, Saint Louis University School of Medicine, 1402 S. Grand Blvd., St. Louis, MO 63104, USA.
Toxics. 2023 Jun 20;11(6):544. doi: 10.3390/toxics11060544.
Pharmaceuticals are widely recognized as potentially hazardous to aquatic ecosystems. In the last two decades, the constant intake of biologically active chemicals used in human healthcare has been related to the growing release of these agents into natural environments. As reported by several studies, various pharmaceuticals have been detected, mainly in surface water (seas, lakes, and rivers), but also in groundwater and drinking water. Moreover, these contaminants and their metabolites can show biological activity even at very low concentrations. This study aimed to evaluate the developmental toxicity of exposure to the chemotherapy drugs gemcitabine and paclitaxel in aquatic environments. Zebrafish () embryos were exposed to doses of gemcitabine 15 μM in combination with paclitaxel 1 μM from 0 to 96 h post-fertilization (hpf) using a fish embryo toxicity test (FET). This study highlights that both gemcitabine and paclitaxel exposure at single non-toxic concentrations affected survival and hatching rate, morphology score, and body length after exposure in combination. Additionally, exposure significantly disturbed the antioxidant defense system and increased ROS in zebrafish larvae. Gemcitabine and paclitaxel exposure caused changes in the expression of inflammation-related, endoplasmic reticulum stress-related (ERS), and autophagy-related genes. Taken together, our findings underline that gemcitabine and paclitaxel increase developmental toxicity in zebrafish embryos in a time-dependent manner.
药物被广泛认为对水生生态系统具有潜在危害。在过去二十年中,人类医疗保健中使用的生物活性化学物质的持续摄入与这些物质向自然环境中的释放不断增加有关。几项研究报告称,已检测到多种药物,主要存在于地表水(海洋、湖泊和河流)中,但也存在于地下水和饮用水中。此外,这些污染物及其代谢物即使在极低浓度下也可能表现出生物活性。本研究旨在评估在水生环境中接触化疗药物吉西他滨和紫杉醇的发育毒性。使用鱼类胚胎毒性试验(FET),将斑马鱼()胚胎在受精后0至96小时(hpf)暴露于15 μM吉西他滨与1 μM紫杉醇的组合剂量下。本研究强调,在单一无毒浓度下接触吉西他滨和紫杉醇都会影响联合暴露后的存活率、孵化率、形态评分和体长。此外,暴露显著扰乱了斑马鱼幼虫的抗氧化防御系统并增加了活性氧。吉西他滨和紫杉醇暴露导致炎症相关、内质网应激相关(ERS)和自噬相关基因的表达发生变化。综上所述,我们的研究结果强调吉西他滨和紫杉醇以时间依赖性方式增加斑马鱼胚胎的发育毒性。