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Polystyrene micro- and nanoplastics cause placental dysfunction in mice†
Katherine C Dibbon1, Grace V Mercer1, Alexandre S Maekawa1
1Department of Chemistry, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, Canada.
Maternal exposure to microplastics and nanoplastics impacts fetal development. Nanoplastics, specifically, show a greater potential to disrupt fetal brain development and may lead to adverse neurodevelopmental outcomes.
Area of Science:
- Environmental Health
- Toxicology
- Developmental Biology
Background:
- Maternal exposure to microplastics and nanoplastics is a growing concern.
- Previous studies indicate potential for fetal growth restriction in mice.
Purpose of the Study:
- To investigate placental and fetal hemodynamic responses to microplastic and nanoplastic exposure in mice.
- To assess the impact of particle size on these responses.
Main Methods:
- Healthy pregnant CD-1 mice were exposed to polystyrene microplastics (5 μm) or nanoplastics (50 nm) via drinking water throughout gestation.
- High-frequency ultrasound was used to measure placental and fetal hemodynamic parameters.
- Control groups received no plastic exposure.
Main Results:
- Both microplastic and nanoplastic exposure caused placental dysfunction, with effects dependent on particle size.
- Microplastic exposure increased umbilical artery blood flow by 48%, while nanoplastic exposure decreased it by 25%.
- Fetuses exposed to both particle types showed reduced middle cerebral artery pulsatility index, indicating fetal brain adaptation to hypoxia. Nanoplastic exposure showed more pronounced effects.
Conclusions:
- Placental dysfunction and fetal hypoxia markers were more severe with nanoplastic exposure.
- Nanoplastic exposure during pregnancy may disrupt fetal brain development, potentially impacting neurodevelopmental outcomes.
- Particle size is a critical factor in the adverse effects of plastic exposure on maternal-fetal hemodynamics.
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