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Polystyrene microplastics induced disturbances in neuronal arborization and dendritic spine density in mice prefrontal cortex

Chemosphere 2024 28 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.
Anjali Suman, Priya Gupta, Priya Gupta, Anjali Suman, Anjali Suman, Anjali Suman, Priya Gupta, Archisman Mahapatra, Archisman Mahapatra, Archisman Mahapatra, Archisman Mahapatra, Archisman Mahapatra, Archisman Mahapatra, Anjali Suman, Anjali Suman, Anjali Suman, Priya Gupta, Priya Gupta, Priya Gupta, Anjali Suman, Anjali Suman, Shubhendu Shekhar Ray, Rahul Kumar Singh Shubhendu Shekhar Ray, Shubhendu Shekhar Ray, Anjali Suman, Shubhendu Shekhar Ray, Rahul Kumar Singh Shubhendu Shekhar Ray, Rahul Kumar Singh Rahul Kumar Singh Rahul Kumar Singh Rahul Kumar Singh

Summary

Mice that consumed polystyrene microplastics for 28 days showed significant damage to brain cells in the prefrontal cortex, the region responsible for decision-making and behavior. The neurons had shorter branches, fewer connections, and reduced levels of a key growth factor called BDNF. These findings suggest that microplastic exposure could affect brain structure and potentially cognitive function, raising concerns about the neurological effects of chronic microplastic ingestion in humans.

Polymers
Body Systems
Models

An increasing use of plastics in daily life leads to the accumulation of microplastics (MPs) in the environment, posing a serious threat to the ecosystem, including humans. It has been reported that MPs cause neurotoxicity, but the deleterious effect of polystyrene (PS) MPs on neuronal cytoarchitectural morphology in the prefrontal cortex (PFC) region of mice brain remains to be established. In the present study, Swiss albino male mice were orally exposed to 0.1, 1, and 10 ppm PS-MPs for 28 days. After exposure, we found a significant accumulation of PS-MPs with a decreased number of Nissl bodies in the PFC region of the entire treated group compared to the control. Morphometric analysis in the PFC neurons using Golgi-Cox staining accompanied by Sholl analysis showed a significant reduction in basal dendritic length, dendritic intersections, nodes, and number of intersections at seventh branch order in PFC neurons of 1 ppm treated PS-MPs. In neurons of 0.1 ppm treated mice, we found only decrease in the number of intersections at the seventh branch order. While 10 ppm treated neurons decreased in basal dendritic length, dendritic intersections, followed by the number of intersections at the third and seventh branch order were observed. As well, spine density on the apical secondary branches along with mRNA level of BDNF was significantly reduced in all the PS-MPs treated PFC neurons, mainly at 1 ppm versus control. These results suggest that PS-MPs exposure affects overall basal neuronal arborization, with the highest levels at 1 and 10 ppm, followed by 0.1 ppm treated neurons, which may be related to the down-regulation of BDNF expression in PFC.

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