虹鳟鱼接触特定药物后的急性暴露和生物标志物评估

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
C. André, J. Auclair, F. Gagné
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引用次数: 0

摘要

城市污水中排放的药物对水生生物构成风险。我们评估了 5 种具有不同治疗作用的药物对虹鳟鱼的毒性:奥氮平(抗精神病药)、红霉素(抗生素)、霉酚酸盐(免疫抑制药)、匹维林(消炎药)和曲唑酮(镇静药)。将幼体暴露于这些药物中 96 小时,药物浓度从 64 微克/升到 40 毫克/升不等,以达到致死目的。在亚致死浓度下,测定存活率并分析药物生物转化、氧化应激/损伤和代谢活动的一系列生物标志物。数据显示了以下毒性:奥氮平>曲唑酮>霉酚酸酯>匹维林∼红霉素(基于死亡率)。数据还显示,毒性与质量、pKa 和疏水性以及以下亚致死效应有关:GST、LPO 和 DNA 链断裂。一般来说,分子量较低、pKa 为生理 pKa、疏水性适中、生物转化率低和 DNA 链断裂的药物对鱼类的毒性更大。不过,这应被视为确定非目标生物中有毒药物的一般指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute exposure and biomarkers assessment in rainbow trout exposed to selected pharmaceuticals

Pharmaceuticals released from municipal effluents discharges pose a risk to aquatic organisms. The toxicity of 5 pharmaceuticals with distinct therapeutic actions were assessed in rainbow trout: olanzapine (antipsychotic), erythromycin (antibiotic), mycophenoate (immunosuppression), pinaverium (anti-inflammatory) and trazodone (sedative). Juveniles were exposed to these drugs for 96 h at concentrations between 64 µg/L up to 40 mg/L to reach lethality. Survival was determined and a suite of biomarkers was analyzed for drug biotransformation, oxidative stress/damage and metabolic activity at sublethal concentrations. The data revealed the following toxicity: olanzapine >trazodone>mycophenolate>pinaverium∼erythromycin based on mortality. The data also revealed that toxicity was associated to mass, pKa and hydrophobicity and the following sublethal effects: GST, LPO and DNA strand breaks. Pharmaceuticals with lower molecular weight, physiological pKa, moderate hydrophobicity, low biotransformation and DNA strand breaks were generally more toxic to fish. However, this should be considered as a general guide in identifying toxic pharmaceuticals in non-target organisms.

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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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