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Comparison of metabolome profiles in zebrafish (Danio rerio) intestine induced by polystyrene microplastics with different sizes

Environmental Science and Pollution Research 2022 23 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 50 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Jing Yu, Jing Yu, Weiqing Gu, Jing Yu, Ling Chen, Weiqing Gu, Bing Wu Ling Chen, Ling Chen, Weiqing Gu, Ling Chen, Weiqing Gu, Ling Chen, Ling Chen, Weiqing Gu, Ling Chen, Ling Chen, Ling Chen, Bing Wu Bing Wu Weiqing Gu, Weiqing Gu, Weiqing Gu, Ling Chen, Jing Yu, Bing Wu Bing Wu Bing Wu Bing Wu Bing Wu Ling Chen, Ling Chen, Bing Wu Ling Chen, Ling Chen, Jing Yu, Ling Chen, Jing Yu, Bing Wu Bing Wu Bing Wu Bing Wu Bing Wu

Summary

Researchers compared metabolic profiles in zebrafish intestines after exposure to polystyrene microplastics of different sizes, finding that smaller particles caused more severe metabolic disruption including altered lipid metabolism and amino acid pathways in a size-dependent manner.

Polymers

Microplastics (MPs) are widespread in aquatic environments. They could induce intestinal toxicity in the fish. However, research on the metabolic toxicity of polystyrene microplastics (PS-MPs) with different particle sizes to the zebrafish intestine is still limited. Here, metabolomics using ultra-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was applied to characterize the metabolic disorders in zebrafish intestine after exposure to 500 μg/L PS-MPs with different sizes (100 nm, 5 μm, and 200 μm) for 21 days. Results showed that the 100 nm PS-MPs group increased glutathione content. A total of 35, 165, and 87 metabolites were significantly altered in zebrafish intestines of 100 nm, 5 μm, and 200 μm groups under positive ion mode, respectively. In comparison, 31, 115, and 45 metabolites were changed in the 100 nm, 5 μm, and 200 μm groups under negative ion mode, respectively. Metabolic pathway analysis indicated that carbohydrate metabolism, amino acid metabolism, and nucleotide metabolism were changed in all three groups. The greatest changes were found in the 5 μm group. Moreover, treatment with micro-sized PS-MP groups specifically changed lipid metabolism, which might be related to pathogenic bacteria (Streptococcus and Moraxella). In the 100 nm PS-MP group, S-adenosyl-L-methionine (SAM) was found to be markedly related to the intestinal microbiota. SAM level was significantly increased, which might account for the elevated glutathione content. To sum up, the mechanisms of nano-sized MPs (oxidative stress) and micro-sized MPs (lipid metabolism disorder) were distinct. This study provides novel insight into the toxicity mechanism of MPs in the zebrafish intestine.

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