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所选精神药物和抗生素对蓝贻贝(紫贻贝)血细胞的遗传毒性和免疫毒性潜在影响。

Genotoxic and immunotoxic potential effects of selected psychotropic drugs and antibiotics on blue mussel (Mytilus edulis) hemocytes.

作者信息

Lacaze Emilie, Pédelucq Julie, Fortier Marlène, Brousseau Pauline, Auffret Michel, Budzinski Hélène, Fournier Michel

机构信息

INRS, Institut Armand-Frappier, 531 des Prairies Blvd., Laval, H7V 1B7 QC, Canada.

INRS, Institut Armand-Frappier, 531 des Prairies Blvd., Laval, H7V 1B7 QC, Canada; EPOC-LPTC, UMR 5805, Université Bordeaux 1, 351 Cours de la Libération, 33405 Talence, France.

出版信息

Environ Pollut. 2015 Jul;202:177-86. doi: 10.1016/j.envpol.2015.03.025. Epub 2015 Mar 30.

Abstract

The potential toxicity of pharmaceuticals towards aquatic invertebrates is still poorly understood and sometimes controversial. This study aims to document the in vitro genotoxicity and immunotoxicity of psychotropic drugs and antibiotics on Mytilus edulis. Mussel hemocytes were exposed to fluoxetine, paroxetine, venlafaxine, carbamazepine, sulfamethoxazole, trimethoprim and erythromycin, at concentrations ranging from μg/L to mg/L. Paroxetine at 1.5 μg/L led to DNA damage while the same concentration of venlafaxine caused immunomodulation. Fluoxetine exposure resulted in genotoxicity, immunotoxicity and cytotoxicity. In the case of antibiotics, trimethoprim was genotoxic at 200 μg/L and immunotoxic at 20 mg/L whereas erythromycin elicited same detrimental effects at higher concentrations. DNA metabolism seems to be a highly sensitive target for psychotropic drugs and antibiotics. Furthermore, these compounds affect the immune system of bivalves, with varying intensity. This attests the relevance of these endpoints to assess the toxic mode of action of pharmaceuticals in the aquatic environment.

摘要

药物对水生无脊椎动物的潜在毒性仍知之甚少,有时还存在争议。本研究旨在记录精神药物和抗生素对紫贻贝的体外遗传毒性和免疫毒性。将贻贝血细胞暴露于氟西汀、帕罗西汀、文拉法辛、卡马西平、磺胺甲恶唑、甲氧苄啶和红霉素中,浓度范围为μg/L至mg/L。1.5μg/L的帕罗西汀导致DNA损伤,而相同浓度的文拉法辛引起免疫调节。氟西汀暴露导致遗传毒性、免疫毒性和细胞毒性。就抗生素而言,200μg/L的甲氧苄啶具有遗传毒性,20mg/L时具有免疫毒性,而红霉素在较高浓度下产生相同的有害影响。DNA代谢似乎是精神药物和抗生素的一个高度敏感靶点。此外,这些化合物以不同强度影响双壳贝类的免疫系统。这证明了这些终点对于评估药物在水生环境中的毒性作用模式的相关性。

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