UMR BOREA (Biologie des ORganismes et Ecosystèmes Aquatiques), CNRS-7208/MNHN/UPMC/IRD-207/UCBN, Esplanade de la Paix, 14032 Caen Cedex, France; CERMN, UFR des Sciences Pharmaceutiques, UPRES EA4258 - FR CNRS INC3M - SF 4206 ICORE, Université de Caen Basse-Normandie, Bd Becquerel, 14032 Caen Cedex, France.
UMR BOREA (Biologie des ORganismes et Ecosystèmes Aquatiques), CNRS-7208/MNHN/UPMC/IRD-207/UCBN, Esplanade de la Paix, 14032 Caen Cedex, France; CERMN, UFR des Sciences Pharmaceutiques, UPRES EA4258 - FR CNRS INC3M - SF 4206 ICORE, Université de Caen Basse-Normandie, Bd Becquerel, 14032 Caen Cedex, France.
Chemosphere. 2014 Aug;108:314-9. doi: 10.1016/j.chemosphere.2014.01.057. Epub 2014 Feb 14.
Currently, the hazard posed by pharmaceutical residues is a major concern of ecotoxicology. Most of the antidepressants belong to a family named the Cationic Amphipathic Drugs known to have specific interactions with cell membranes. The present study assessed the impact of eight antidepressants belonging to selective serotonin reuptake inhibitors or serotonin norepinephrine reuptake inhibitors by the combination of multi-approaches (in vivo, in vitro, in silico) and gives some insights on the mode of action for these molecules. Antidepressants were from the most to the least toxic compound for Daphnia magna: Sertraline (EC50=1.15 mg L(-1))>Clomipramine (2.74 mg L(-1))>Amitriptyline (4.82 mg L(-1))>Fluoxetine (5.91 mg L(-1))>Paroxetine (6.24 mg L(-1))>Mianserine (7.81 mg L(-1))>Citalopram (30.14 mg L(-1)) and Venlafaxine (141.28 mg L(-1)). These acute toxicities were found correlated to Log Kow coefficients (R=0.93, p<0.001) and to cytotoxicity assessed on abalone hemocytes through the neutral red uptake assay (R=0.96, p<0.001). If narcosis as mode of action is typically expected during acute ecotoxicity bioassays, we showed by molecular modeling that particular interactions can exist between antidepressants and phosphatidylcholine, a major component of cell membranes, leading to a more specific mode of action corresponding to a potential acidic hydrolysis of ester functions.
目前,药物残留造成的危害是生态毒理学关注的主要问题。大多数抗抑郁药属于阳离子两亲性药物家族,已知其与细胞膜有特定的相互作用。本研究通过多途径(体内、体外、计算)评估了属于选择性 5-羟色胺再摄取抑制剂或 5-羟色胺去甲肾上腺素再摄取抑制剂的八种抗抑郁药的影响,并为这些分子的作用模式提供了一些见解。抗抑郁药对大型溞的毒性从大到小依次为:舍曲林(EC50=1.15mg/L)>氯米帕明(2.74mg/L)>阿米替林(4.82mg/L)>氟西汀(5.91mg/L)>帕罗西汀(6.24mg/L)>米氮平(7.81mg/L)>西酞普兰(30.14mg/L)和文拉法辛(141.28mg/L)。这些急性毒性与 Log Kow 系数(R=0.93,p<0.001)和通过中性红摄取试验评估的对鲍鱼血细胞的细胞毒性相关(R=0.96,p<0.001)。如果麻醉作用通常是急性生态毒性生物测定中的作用模式,我们通过分子建模表明,抗抑郁药与细胞膜的主要成分磷脂酰胆碱之间可能存在特定的相互作用,导致更特定的作用模式,对应于酯功能的潜在酸性水解。