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Maternal exposure to polystyrene microplastics impairs social behavior in mouse offspring with a potential neurotoxicity

NeuroToxicology 2023 43 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.
Yun Hee So, Hyun Seung Shin, Seung‐Hyun Lee, Ha Jung Moon, Hyeon Jung Jang, Eun‐Hee Lee, Eui‐Man Jung

Summary

When pregnant mice were exposed to polystyrene microplastics, their offspring showed impaired social behavior even though the plastics did not reach the brain directly. The microplastics accumulated in the mothers' digestive organs and caused changes in brain cell growth and survival in isolated neurons. This study suggests that microplastic exposure during pregnancy could affect brain development and social behavior in offspring through indirect mechanisms.

Polymers
Models

As plastic production has been increasing steadily, environmental pollution resulting from microplastics (MPs) continues to draw considerable attention of the researchers. Several studies have reported that MPs are risk factors for various cellular and systemic dysfunctions. However, the effects of chronic MP exposure from the embryonic stage to adulthood on mouse brain remain unclear. Accordingly, determining the impacts of maternal exposure to MPs on mouse offspring was the main goal of this study. To this end, single cells of primary cortical neurons were isolated from mouse embryos. Subsequently, the cells were exposed to 2 µm polystyrene microplastics (PS-MPs), which resulted in a notable reduction in dendritic length, and PS-MPs cannot pass through the cellular membrane of neurons. Moreover, exposure to PS-MPs caused the proliferation increase and apoptosis in primary cortical neuronal cells. We then evaluated the neurotoxicity associated with chronic PS-MP exposure from the embryonic stage to adulthood in C57BL/6 J mouse offspring. PS-MPs were found to accumulate in the digestive and excretory organs of the offspring but not in the brain tissue. However, offspring exposed to PS-MPs exhibited no differences in the levels of expression of genes related to brain cell markers or synaptic organization. Nevertheless, PS-MP-exposed mice exhibited impaired social novelty preferences; however, no changes were observed in the emotional, compulsive, or cognitive behaviors. Taken together, these results demonstrate the potential neurotoxic effects of chronic exposure to PS-MPs in mouse offspring.

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