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Effects of nano- and microplastics on kidney: Physicochemical properties, bioaccumulation, oxidative stress and immunoreaction

Chemosphere 2021 213 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 60 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Xuemei Meng, Xuemei Meng, Xuemei Meng, Xuemei Meng, Xuemei Meng, Xuemei Meng, Xuemei Meng, Jiawei Zhang, Wenjing Wang, Wenjing Wang, Jiawei Zhang, Jiawei Zhang, Wenjing Wang, Zhenyu Li G. González-Gil, Johannes S. Vrouwenvelder, G. González-Gil, Wenjing Wang, Johannes S. Vrouwenvelder, Johannes S. Vrouwenvelder, Wenjing Wang, Zhenyu Li Zhenyu Li Wenjing Wang, Zhenyu Li

Summary

Researchers exposed mice to polystyrene nano- and microplastics of varying sizes and tracked their accumulation and effects in the kidneys. They found that the particles changed their physical properties during digestion, accumulated in kidney tissue, and caused oxidative stress and immune responses. The study suggests that plastic particle size plays an important role in determining the extent of kidney-related harm.

Polymers
Models

The potential toxicity of nanoplastics (NPs) and microplastics (MPs) has raised concerns. However, knowledge of the effects of NPs/MPs on the health of mammals is still limited. Here we investigated the alteration of the physicochemical properties of polystyrene NPs (PS-NPs: 50 nm) and MPs (PS-MPs: 300 nm, 600 nm, 4 μm) in the gastrointestinal tract. Moreover, we investigated the uptake and bioaccumulation and the toxic effects of these plastic particles in the kidneys of mice. The results revealed that their digestion promoted the aggregation of PS-NPs and PS-MPs and increased the Zeta-potential value. Both PS-NPs and PS-MPs bioaccumulated in the kidneys, and the aggregation of 600 nm PS-MPs exacerbated their biotoxicity. The PS-NPs and PS-MPs caused mice weight loss, increased their death rate, significantly alternated several biomarkers, and resulted in histological damage of the kidney. We also found that exposure to PS-NPs and PS-MPs induced oxidative stress and the development of inflammation. These findings provide new insights into the toxic effects of NPs and MPs on mice.

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