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Chronic Exposure to Microplastics Induces Blood–Brain Barrier Impairment, Oxidative Stress, and Neuronal Damage in Rats

Molecular Neurobiology 2025 7 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 63 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Ghasem Forutan, Ghasem Forutan, Reza Dehbandi Yaghoob Farbood, Reza Dehbandi Reza Dehbandi Alireza Sarkaki, Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Samireh Ghafouri, Somayeh Hajipour, Reza Dehbandi Reza Dehbandi Reza Dehbandi Yaghoob Farbood, Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi Reza Dehbandi

Summary

Rats that were fed low-density polyethylene microplastics for up to six weeks developed significant brain damage, including a weakened blood-brain barrier (the protective shield that keeps harmful substances out of the brain), increased oxidative stress, and neuron death. The longer the exposure lasted, the worse the damage became, with a key brain-health protein called BDNF declining significantly by week six. This study provides strong evidence that chronic microplastic exposure could harm brain health by allowing toxic substances to enter the brain more easily.

Polymers
Body Systems
Models

The widespread prevalence of plastics and in particular, microplastics (MPs) raises concerns about their potential toxic effects. MPs, defined as particles smaller than 5 mm, are distributed throughout ecosystem and can enter the human body through the food chain. There is a lack of knowledge regarding MP potential harmful effects on the mammal's body, especially the brain. This study aimed to examine the impact of low-density polyethylene (LDPE) MPs (< 30 μm) on blood-brain barrier (BBB) integrity, oxidative stress, and neuronal health. Male rats were exposed to LDPE MPs via oral administration for 3 and 6 weeks. The results revealed no significant changes in brain water content across groups. However, BBB integrity was significantly compromised after both 3 and 6 weeks of exposure. Oxidative stress increased in MP-treated groups, evidenced by decreased superoxide dismutase (SOD) levels and elevated malondialdehyde (MDA). Additionally, brain-derived neurotrophic factor (BDNF) levels significantly declined in the 6-week group. Histological analysis indicated neuronal damage and death in both treatment durations. These findings demonstrate that chronic exposure to LDPE MPs impairs BBB integrity, increases oxidative stress, and induces neuronal damage in rats. The results highlight the neurotoxic potential of MPs and emphasize the need for further research to address their possible health risks.

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