Rodrigues P, Cunha V, Oliva-Teles L, Ferreira M, Guimarães L
CIIMAR/CIMAR - Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Avenida General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal.
CIIMAR/CIMAR - Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Avenida General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal; Faculdade de Ciências da Universidade do Porto, Rua do Campo Alegre, s/n, 4169-007, Porto, Portugal.
J Hazard Mater. 2020 Dec 5;400:123171. doi: 10.1016/j.jhazmat.2020.123171. Epub 2020 Jun 17.
Antidepressant metabolites are found in natural and waste waters. However, investigation of their toxic effects on aquatic animals, single or in mixture with other occurring psychoactive drugs, has been neglected. Here, effects of 80hpf exposure to norfluoxetine (0.64-400 ng/L), venlafaxine (16-10000 ng/L) or their combination (3.2 ng/L +2000 ng/L, respectively) were investigated in embryos and zebrafish larvae. Mortality, embryonic malformations, sensorymotor reflexes and the expression of 34 genes involved in the toxicants mode-of-action (MoA) and metabolism were evaluated (i.e. monoamine receptors and transporters, nuclear receptors, and detoxification transporters and enzymes). Compared to controls, norfluoxetine treatments only caused depigmentation of embryos and larvae. Venlafaxine-exposed larvae exhibited depigmentation and spinal deformities, impaired sensorymotor reflexes, alterations in the expression of genes belonging to the serotonergic, noradrenergic and dopaminergic pathways, as well as nuclear receptors related to lipid and drug metabolism. The mixture elicited distinct interaction effects, depending on the level of biological organisation analysed and the neurotransmitter pathways affected; synergism (lethality), no interaction (sensorymotor reflexes), antagonism and inverse agonism (gene expression). The results call for investigation of the toxicity of pharmaceutical metabolites single and in mixture, as well as their risk assessment in approaches accounting for possible interactions with other endocrine-disrupting compounds.
抗抑郁药代谢产物存在于天然水体和废水中。然而,关于它们对水生动物的毒性影响,无论是单独的还是与其他共存的精神活性药物混合后的影响,都一直被忽视。在此,研究了在胚胎和斑马鱼幼体中暴露于去甲氟西汀(0.64 - 400纳克/升)、文拉法辛(16 - 10000纳克/升)或它们的组合(分别为3.2纳克/升 + 2000纳克/升)80小时后的影响。评估了死亡率、胚胎畸形、感觉运动反射以及34个参与毒物作用模式(MoA)和代谢的基因的表达(即单胺受体和转运体、核受体以及解毒转运体和酶)。与对照组相比,去甲氟西汀处理仅导致胚胎和幼体色素脱失。暴露于文拉法辛的幼体表现出色素脱失和脊柱畸形、感觉运动反射受损以及属于血清素能、去甲肾上腺素能和多巴胺能途径的基因表达改变,以及与脂质和药物代谢相关的核受体改变。该混合物根据所分析的生物组织水平和受影响的神经递质途径产生了不同的相互作用效应;协同作用(致死性)、无相互作用(感觉运动反射)、拮抗作用和反向激动作用(基因表达)。这些结果呼吁对药物代谢产物单独和混合时的毒性进行研究,以及在考虑与其他内分泌干扰化合物可能相互作用的方法中对它们进行风险评估。