首页> 外文期刊>Aquatic Toxicology >Transcriptional and cellular effects of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in experimentally exposed mussels, Mytilus galloprovincialis
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Transcriptional and cellular effects of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in experimentally exposed mussels, Mytilus galloprovincialis

机译:非甾体抗炎药(NSAIDs)在实验暴露的贻贝Mytilus galloprovincialis中的转录和细胞作用

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The aim of the present investigation was to provide new insights on accumulation and possible adverse effects of various non-steroidal anti-inflammatory drugs (NSAIDs) in mussels, Mytilus gallo-provincialis, exposed to an environmentally realistic concentration (0.5 mu g/L) of individual compounds, Acetaminophen (AMP), Diclofenac (DIC), Ibuprofen (IBU), Ketoprofen (KET) or Nimesulide (NIM). The measurement of drugs in mussel tissues was integrated with both functional alterations at cellular level and transcriptomic responses. Results indicated the capability of mussels to accumulate DIC and NIM, while AMP, IBU and KET were always below detection limit. A large panel of ecotoxicological biomarkers revealed the early onset of alterations induced by tested NSAIDs on immunological responses, lipid metabolism and DNA integrity. The gene transcription analysis through DNA microarrays, supported cellular biomarker results, with clear modulation of a large number of genes involved in the arachidonic acid and lipid metabolism, immune responses, cell cycle and DNA repair. The overall results indicated an ecotoxicological concern for pharmaceuticals in M. galloprovincialis, with transcriptional responses appearing as sensitive exposure biomarkers at low levels of exposure: such changes, however, are not always paralleled by corresponding functional effects, suggesting caution when interpreting observed effects in terms of perturbed cellular pathways. Fascinating similarities can also be proposed in the mode of action of NSAIDs between bivalves and vertebrate species. (C) 2016 Elsevier B.V. All rights reserved.
机译:本研究的目的是就暴露于环境中实际浓度(0.5μg / L)的贻贝(Mytilus gallo-provincialis)贻贝中各种非甾体类抗炎药(NSAIDs)的蓄积和可能的不良影响提供新的见解。对乙酰氨基酚(AMP),双氯芬酸(DIC),布洛芬(IBU),酮洛芬(KET)或尼美舒利(NIM)的化合物。贻贝组织中药物的测量与细胞水平上的功能改变和转录组反应相结合。结果表明贻贝积累DIC和NIM的能力,而AMP,IBU和KET始终低于检出限。大量生态毒理学生物标志物揭示了受试NSAID在免疫应答,脂质代谢和DNA完整性方面引起的改变的早期发作。通过DNA芯片进行的基因转录分析,支持了细胞生物标志物的结果,对涉及花生四烯酸和脂质代谢,免疫反应,细胞周期和DNA修复的大量基因进行了清晰的调节。总体结果表明,对于在墨西哥省分枝杆菌中的药物而言,存在一种生态毒理学问题,其转录反应在低暴露水平下表现为敏感的暴露生物标志物;但是,这种变化并不总是与相应的功能作用平行,建议在解释观察到的作用时要谨慎扰动的细胞途径。在双壳类和脊椎动物之间的非甾体抗炎药的作用方式上也可以提出令人着迷的相似性。 (C)2016 Elsevier B.V.保留所有权利。

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