Literature DB >> 32036646

Biotransformation Changes Bioaccumulation and Toxicity of Diclofenac in Aquatic Organisms.

Qiuguo Fu1, Davide Fedrizzi1, Verena Kosfeld2,3, Christian Schlechtriem2,3, Vera Ganz1,4, Samuel Derrer1, Daniel Rentsch5, Juliane Hollender1,4.   

Abstract

Biotransformation plays a crucial role in regulating the bioaccumulation potential and toxicity of organic compounds in organisms but is, in general, poorly understood for emerging contaminants. Here, we have used diclofenac as a model compound to study the impact of biotransformation on the bioaccumulation potential and toxicity in two keystone aquatic invertebrates: Gammarus pulex and Hyalella azteca. In both species, diclofenac was transformed into several oxidation products and conjugates, including two novel products, that is, diclofenac taurine conjugate (DCF-M403) and unexpected diclofenac methyl ester (DCF-M310.03). The ratios of biotransformation products to parent compound were 12-17 for DCF-M403 and 0.01-0.7 for DCF-M310.03 after 24 h exposure. Bioconcentration factors (BCFs) of diclofenac were 0.5 and 3.2 L kgww-1 in H. azteca and G. pulex, respectively, whereas BCFs of DCF-M310.03 was 164.5 and 104.7 L kgww-1, respectively, representing a 25- to 110-fold increase. Acute toxicity of DCF-M310.03 was also higher than the parent compound in both species, which correlated well with the increased bioconcentration potential. The LC50 of diclofenac in H. azteca was 216 mg L-1, while that of metabolite DCF-M310.03 was reduced to only 0.53 mg L-1, representing a 430-fold increase in acute toxicity compared to diclofenac. DCF-M403 is less toxic than its parent compound toward H. azteca, which may be linked to its slightly lower hydrophobicity. Furthermore, the transformation of diclofenac to its methyl ester derivative was explored in crude invertebrate extracts spiked with an S-adenosylmethionine cofactor, revealing possible catalysis by an S-adenosylmethionine-dependent carboxylic acid methyltransferase. Methylation of diclofenac was further detected in fish hepatocytes and human urine, indicating a broader relevance. Therefore, potentially methylated metabolites of polar contaminants should be considered for a comprehensive risk assessment in the future.

Entities:  

Year:  2020        PMID: 32036646     DOI: 10.1021/acs.est.9b07127

Source DB:  PubMed          Journal:  Environ Sci Technol        ISSN: 0013-936X            Impact factor:   9.028


  4 in total

Review 1.  Non-steroidal anti-inflammatory drugs in the era of the Covid-19 pandemic in the context of the human and the environment.

Authors:  Danuta Wojcieszyńska; Henryk Guzik; Urszula Guzik
Journal:  Sci Total Environ       Date:  2022-04-19       Impact factor: 10.753

2.  Diclofenac Degradation-Enzymes, Genetic Background and Cellular Alterations Triggered in Diclofenac-Metabolizing Strain Pseudomonas moorei KB4.

Authors:  Joanna Żur; Artur Piński; Danuta Wojcieszyńska; Wojciech Smułek; Urszula Guzik
Journal:  Int J Mol Sci       Date:  2020-09-16       Impact factor: 5.923

Review 3.  Transformation Products of Emerging Pollutants Explored Using Non-Target Screening: Perspective in the Transformation Pathway and Toxicity Mechanism-A Review.

Authors:  Thodhal-Yoganandham Suman; Soo-Yeon Kim; Dong-Hyuk Yeom; Junho Jeon
Journal:  Toxics       Date:  2022-01-24

4.  Development of a method for assessing the accumulation and metabolization of antidepressant drugs in zebrafish (Danio rerio) eleutheroembryos.

Authors:  Noemí Molina-Fernández; Sandra Rainieri; Riansares Muñoz-Olivas; Paloma de Oro-Carretero; Jon Sanz-Landaluze
Journal:  Anal Bioanal Chem       Date:  2021-06-30       Impact factor: 4.142

  4 in total

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