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Polystyrene nanoparticles aggravate the adverse effects of di-(2-ethylhexyl) phthalate on different segments of intestine in mice

Chemosphere 2022 17 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 45 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Ziying Yu, Ziying Yu, Lixiao Zhou, Yinyin Xia, Ziying Yu, Ziying Yu, Wei Sun, Shixin Tang, Shuqun Cheng, Xuejun Jiang Yinyin Xia, Ziying Yu, Lejiao Mao, Lejiao Mao, Ziying Yu, Yinyin Xia, Yinyin Xia, Shiyue Luo, Shiyue Luo, Shixin Tang, Shixin Tang, Shuqun Cheng, Shuqun Cheng, Wei Sun, Lejiao Mao, Xuejun Jiang Wei Sun, Lejiao Mao, Xuejun Jiang Shiyue Luo, Shiyue Luo, Zhen Zou, Lejiao Mao, Shixin Tang, Zhen Zou, Lejiao Mao, Shixin Tang, Chengzhi Chen, Chengzhi Chen, Zhen Zou, Jingfu Qiu, Zhen Zou, Jingfu Qiu, Chengzhi Chen, Jingfu Qiu, Lixiao Zhou, Chengzhi Chen, Jingfu Qiu, Lixiao Zhou, Xuejun Jiang

Summary

Researchers exposed mice to polystyrene nanoparticles and the plasticizer DEHP simultaneously, finding that co-exposure caused greater intestinal damage — including shorter villi, disrupted tight junctions, and reduced mucus coverage — than either contaminant alone, with gut microbiota alterations likely contributing to the enhanced toxicity.

Emerging evidence indicates that nanoplastics (NPs) can transport organic pollutants such as di-(2-ethylhexyl) phthalate (DEHP) into organisms and induce adverse health effects. Nevertheless, the toxic effects of NPs combined with DEHP on mammalian intestine are still unclear. In this study, the C57BL6J mice were exposed to polystyrene nanoparticles (PSNPs), DEHP or them both for 30 days to determine their effects on different segments of intestine and the gut microbiota. As a result, DEHP alone or co-exposure to DEHP and PSNPs induced histological damages in all intestinal parts, mainly manifested as the decreased villus lengths, increased crypt depths in the duodenum, jejunum and ileum and decreased villus counts accompanied with decreased epithelial area in the colon. Moreover, decreased mucus coverage, down-regulated Muc2 expression levels as well as the broken tight junctions were observed in intestinal epithelium of mice, particularly obvious in the co-treatment groups. In general, as manifested by greater alterations in most of the parameters mentioned above, simultaneously exposed to PSNPs and DEHP seemed to induce enhanced toxic effects on intestine of mouse when compared with DEHP alone. Furthermore, the altered community composition of gut microbiota might at least partially contribute to these abnormalities. Overall, our results highlight the aggravated toxicity on different segments of intestine in mammalians due to co-exposure of PSNPs and DEHP, and these findings will provide valuable insights into the health risk of NPs and plastic additives.

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