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A preliminary study about the potential risks of the UV-weathered microplastic: The proteome-level changes in the brain in response to polystyrene derived weathered microplastics

Environmental Research 2023 38 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Hee-Yeon Kim, Janbolat Ashim, Song Park, Wan-Soo Kim, Sangho Ji, Seoung-Woo Lee, Yi-Rang Jung, Sang Won Jeong, Se-Guen Lee, Hyun-Chul Kim, Young Jae Lee, Mi Kyung Kwon, Junseong Hwang, Jung Min Shin, Sungjun Lee, Wookyung Yu, Jin-Kyu Park, Jin‐Kyu Park, Seong‐Kyoon Choi

Summary

Researchers found that UV-weathered microplastics, which more closely resemble real-world plastic pollution, caused greater changes to brain proteins in mice than pristine microplastics. The weathered particles triggered alterations in proteins related to nerve signaling and cellular stress responses. This suggests that the microplastics people actually encounter in the environment may be more neurotoxic than the pristine particles typically used in lab studies.

Polymers
Body Systems
Models
Study Type In vitro

The growing use of plastic materials has resulted in a constant increase in the risk associated with microplastics (MPs). Ultra-violet (UV) light and wind break down modify MPs in the environment into smaller particles known as weathered MPs (WMPs) and these processes increase the risk of MP toxicity. The neurotoxicity of weathered polystyrene-MPs remains unclear. Therefore, it is important to understand the risks posed by WMPs. We evaluated the chemical changes of WMPs generated under laboratory-synchronized environmentally mimetic conditions and compared them with virgin MPs (VMPs). We found that WMP had a rough surface, slight yellow color, reduced molecular weight, and structural alteration compared with those of VMP. Next, 2 μg of ∼100 μm in size of WMP and VMP were orally administered once a day for one week to C57BL/6 male mice. Proteomic analysis revealed that the WMP group had significantly increased activation of immune and neurodegeneration-related pathways compared with that of the VMP group. Consistently, in in vitro experiments, the human brain-derived microglial cell line (HMC-3) also exhibited a more severe inflammatory response to WMP than to VMP. These results show that WMP is a more profound inflammatory factor than VMP. In summary, our findings demonstrate the toxicity of WMPs and provide theoretical insights into their potential risks to biological systems and even humans in the ecosystem.

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