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淡水蜗牛椎实螺对水生污染物双氯芬酸的代谢

Metabolism of the aquatic pollutant diclofenac in the Lymnaea stagnalis freshwater gastropod.

作者信息

Bouly Lucie, Fenet Hélène, Carayon Jean-Luc, Gomez Elena, Géret Florence, Courant Frédérique

机构信息

Biochimie Et Toxicologie Des Substances Bioactives, EA 7417, INU Champollion, Albi, France.

HydroSciences Montpellier, University of Montpellier, IRD, CNRS, 15 avenue Charles Flahault, 34093, Montpellier, France.

出版信息

Environ Sci Pollut Res Int. 2022 Dec;29(56):85081-85094. doi: 10.1007/s11356-022-21815-5. Epub 2022 Jul 6.

Abstract

The metabolism of organic contaminants in Lymnaea stagnalis freshwater gastropod remains unknown. Yet, pharmaceuticals-like the NSAID diclofenac-are continuously released in the aquatic environment, thereby representing a risk to aquatic organisms. In addition, lower invertebrates may be affected by this pollution since they are likely to bioaccumulate contaminants. The metabolism of pharmaceuticals in L. stagnalis requires further investigation to understand their detoxification mechanisms and characterized the risk posed by contaminant exposure in this species. In this study, a non-targeted strategy using liquid chromatography combined with high-resolution mass spectrometry was applied to highlight metabolites formed in L. stagnalis freshwater snails exposed to 300 µg/L diclofenac for 3 and 7 days. Nineteen metabolites were revealed by this approach, 12 of which were observed for the first time in an aquatic organism exposed to diclofenac. Phase I metabolism involved hydroxylation, with detection of 3'-, 4'-, and 5-hydroxydiclofenac and three dihydroxylated metabolites, as well as cyclization, oxidative decarboxylation, and dehydrogenation, while phase II metabolism consisted of glucose and sulfate conjugation. Among these reactions, the two main DCF detoxification pathways detected in L. stagnalis were hydroxylation (phase I) and glucosidation (phase II).

摘要

椎实螺(Lymnaea stagnalis)这种淡水腹足纲动物体内有机污染物的代谢情况仍不清楚。然而,像非甾体抗炎药双氯芬酸这类药物不断释放到水生环境中,对水生生物构成了风险。此外,较低等的无脊椎动物可能会受到这种污染的影响,因为它们可能会生物累积污染物。椎实螺体内药物的代谢情况需要进一步研究,以了解其解毒机制,并确定该物种接触污染物所带来的风险。在本研究中,采用了液相色谱结合高分辨率质谱的非靶向策略,以突出暴露于300μg/L双氯芬酸3天和7天的椎实螺淡水蜗牛体内形成的代谢产物。通过这种方法揭示了19种代谢产物,其中12种是首次在暴露于双氯芬酸的水生生物中观察到的。I相代谢包括羟基化反应,检测到了3' -、4' -和5 -羟基双氯芬酸以及三种二羟基化代谢产物,还有环化、氧化脱羧和脱氢反应,而II相代谢则包括葡萄糖和硫酸盐结合反应。在这些反应中,在椎实螺中检测到的两种主要双氯芬酸解毒途径是羟基化(I相)和葡萄糖苷化(II相)。

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