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Gastrointestinal Incomplete Degradation Exacerbates Neurotoxic Effects of PLA Microplastics via Oligomer Nanoplastics Formation

Advanced Science 2024 35 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 65 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Boxuan Liang, Yanhong Deng, Yanhong Deng, Yizhou Zhong, Xiaohong Chen, Yuji Huang, Yuji Huang, Zhiming Li, Xiyun Huang, Xiaohong Yang, Xiaohong Yang, Jiaxin Du, Rongyi Ye, Hongyi Xian, Hongyi Xian, Yujie Feng, Ruobing Bai, Bingchi Fan, Xingfen Yang, Zhenlie Huang

Summary

This study found that when PLA microplastics -- a common biodegradable plastic -- are partially broken down in the digestive system, they form smaller oligomer nanoplastics that are actually more toxic to the brain than the original particles. Mice exposed to these digestive breakdown products showed worse neurological effects, challenging the assumption that biodegradable plastics are inherently safer for human health.

Polymers
Models
Study Type In vivo

Biodegradable plastics, hailed for their environmental friendliness, may pose unforeseen risks as they undergo gastrointestinal degradation, forming oligomer nanoplastics. Despite this, the influence of gastrointestinal degradation on the potential human toxicity of biodegradable plastics remains poorly understood. To this end, the impact of the murine in vivo digestive system is investigated on the biotransformation, biodistribution, and toxicity of PLA polymer and PLA oligomer MPs. Through a 28-day repeated oral gavage study in mice, it is revealed that PLA polymer and oligomer microplastics undergo incomplete and complete degradation, respectively, in the gastrointestinal tract. Incompletely degraded PLA polymer microplastics transform into oligomer nanoplastics, heightening bioavailability and toxicity, thereby exacerbating overall toxic effects. Conversely, complete degradation of PLA oligomer microplastics reduces bioavailability and mitigates toxicity, offering a potential avenue for toxicity reduction. Additionally, the study illuminates shared targets and toxicity mechanisms in Parkinson's disease-like neurotoxicity induced by both PLA polymer and PLA oligomer microplastics. This involves the upregulation of MICU3 in midbrains, leading to neuronal mitochondrial calcium overload. Notably, neurotoxicity is mitigated by inhibiting mitochondrial calcium influx with MCU-i4 or facilitating mitochondrial calcium efflux with DBcAMP in mice. These findings enhance the understanding of the toxicological implications of biodegradable microplastics on human health.

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Gastrointestinal Incomplete Degradation Exacerbates Neurotoxic Effects of PLA Microplastics via Oligomer Nanoplastics Formation (Adv. Sci. 28/2024)

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