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Microplastic polyethylene induced inner ear dysfunction in murine model

Journal of Hazardous Materials 2024 8 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Javeria Zaheer, Javeria Zaheer, Javeria Zaheer, Hyeongi Kim, Seungyoun Kim, Javeria Zaheer, Hyeongi Kim, Hyeongi Kim, Hyeongi Kim, Javeria Zaheer, Jin Su Kim, Seungyoun Kim, Ho‐Sun Lee, Javeria Zaheer, Javeria Zaheer, Javeria Zaheer, Seungyoun Kim, Jin Su Kim, Javeria Zaheer, Jaehee Jang, Seungyoun Kim, Jaehee Jang, Seungyoun Kim, Seungyoun Kim, Jaehee Jang, Jonghoon Choi Jaehee Jang, Jin Su Kim, Jin Su Kim, Jin Su Kim, Jin Su Kim, Jonghoon Choi Jonghoon Choi Jonghoon Choi Jonghoon Choi Jonghoon Choi Jonghoon Choi Jonghoon Choi Hyeongi Kim, Jonghoon Choi Jonghoon Choi Jin Su Kim, Jonghoon Choi Min‐Hyun Park, Jin Su Kim, Jonghoon Choi Jonghoon Choi Seungyoun Kim, Jin Su Kim, Jonghoon Choi Jonghoon Choi Jin Su Kim, Jin Su Kim, Jonghoon Choi Jin Su Kim, Jin Su Kim, Jonghoon Choi

Summary

Researchers exposed mice to polyethylene microplastics and found evidence of inner ear dysfunction, including hearing loss and balance problems. The microplastics triggered changes in gene activity and brain metabolism associated with auditory processing. The study provides the first evidence suggesting that microplastic exposure may affect hearing and balance, opening a new area of health concern.

Polymers
Body Systems
Models

While the hazardous effects of microplastics (MPs) are increasingly reported, it remains uncertain if MPs induce inner ear dysfunction. Nonetheless, prevalence of inner ear dysfunction was observed across all age groups. In this study, we investigated whether MP polyethylene affect inner ear function in a murine model. To detect hearing loss and balance defect after polyethylene (PE) exposure, we evaluated hearing threshold levels, assessed cerebral glucose metabolism, conducted transcriptome analysis, and performed behavioral studies. C57BL/6 J mice (5-week-old) were grouped into control (n = 10) and PE-fed groups (n = 10). Mice were orally administered 100 ppm/100 μL (equivalent to 10 μg) of PE every day for 4 months. We identified the accumulation of PE in the cochlea and vestibular region. The fragmented PE in inner ear was 3.00 ± 0.38 µm in size; the administered PE concentration was 1.14 ± 1.06 mg/g. Fourier transform infrared spectrometry confirmed that the properties of the MP were identical with those of PE fed to the mice. Transcriptomic analysis showed up-regulation of PER1, NR4A3 and CEBPB at the PE exposed inner ear tissue and it was confirmed using qRT-PCR, western blotting, and immunofluorescence staining. We observed abnormalities in balance related behavior assessment in the PE group. Exposure to PE increased the hearing thresholds and decreased glucose metabolism in the bilateral lateral entorhinal cortex, right primary auditory cortex, and right secondary auditory cortex. We can conclude that PE exposure induced inner ear dysfunction such as hearing loss and balance disorder.

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