Normandie Université, F-14032 Caen, France; Centre d'Etudes et de Recherche sur le Médicament de Normandie, UPRES EA-4258, INC3M FR CNRS 3038, SFR ICORE, Université de Caen Basse-Normandie, UFR des Sciences pharmaceutiques, Boulevard Becquerel, F-14032 Caen cedex, France.
Normandie Université, F-14032 Caen, France; Centre d'Etudes et de Recherche sur le Médicament de Normandie, UPRES EA-4258, INC3M FR CNRS 3038, SFR ICORE, Université de Caen Basse-Normandie, UFR des Sciences pharmaceutiques, Boulevard Becquerel, F-14032 Caen cedex, France; CNRS INEE, FRE3484 BioMEA, SFR ICORE, IBFA Université de Caen Basse-Normandie, IBFA, Esplanade de la Paix, F-14032 Caen, France.
Chemosphere. 2014 Sep;110:120-8. doi: 10.1016/j.chemosphere.2014.02.023. Epub 2014 Mar 13.
The present study was conducted to determine the toxicity of different polychlorinated biphenyls (PCBs) on the green algae, Pseudokirchneriella subcapitata and the haemocytes from the European abalone, Haliotis tuberculata. Using the algal growth inhibition test, the green algae median Effective Concentration (EC50) values ranged from 0.34μM for PCB28 to more than 100μM for PCBs 101 and 153. Considering the MTT viability test, the abalone EC50 values ranged from 1.67μM for PCB153 to 89μM for PCB28. Our results in contrast to previous observation in vertebrates did not show significant differences between the dioxin like- and non dioxin like-PCBs toxicities regardless of the model used. However, our results demonstrated that the toxicities of PCBs were species dependent. For example, PCB28 was the most toxic compound for P. subcapitata whereas PCBs 1, 180 and 153 were less toxic for that species. On the contrary, PCB153 was reported as the most toxic for H. tuberculata haemocytes and PCB28 the least toxic. To investigate the mode of action of these compounds, we used an in silico method. Our results suggested that PCBs have a non-specific mode of action (e.g., narcosis) on green algae, and another mode of action, probably more specific than narcosis, was reported for PCBs on the abalone haemocytes.
本研究旨在确定不同多氯联苯(PCBs)对绿藻假鱼腥藻和欧洲鲍血细胞的毒性。采用藻类生长抑制试验,绿藻半数有效浓度(EC50)值范围从 PCB28 的 0.34μM 到 PCB101 和 PCB153 的 100μM 以上。根据 MTT 活力试验,鲍血细胞 EC50 值范围从 PCB153 的 1.67μM 到 PCB28 的 89μM。与以往在脊椎动物中的观察结果相反,无论使用哪种模型,我们的结果都没有显示出类似二恶英和非类似二恶英 PCBs 毒性之间的显著差异。然而,我们的结果表明,PCBs 的毒性具有物种依赖性。例如,PCB28 对假鱼腥藻的毒性最大,而对该物种而言,PCB1、180 和 153 的毒性较小。相反,据报道,PCB153 对 H. tuberculata 血细胞的毒性最大,而 PCB28 的毒性最小。为了研究这些化合物的作用模式,我们使用了一种计算机模拟方法。我们的结果表明,PCBs 对绿藻具有非特异性的作用模式(例如,麻醉),而对鲍血细胞而言,PCBs 可能具有比麻醉更特异性的作用模式。