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Polystyrene micro- and nanoplastics cause placental dysfunction in mice

Biology of Reproduction 2023 45 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.
Katherine Dibbon, Katherine Dibbon, Jenna Hanrahan, Grace V. Mercer, Myrna J. Simpson, Katherine Dibbon, Katherine Dibbon, Jenna Hanrahan, Grace V. Mercer, Grace V. Mercer, Grace V. Mercer, John G. Sled, Lauren C.M. Ringer, Jenna Hanrahan, Katherine L. Steeves, Grace V. Mercer, Grace V. Mercer, Grace V. Mercer, Katherine L. Steeves, Jenna Hanrahan, Lauren C.M. Ringer, Grace V. Mercer, Lindsay S. Cahill Alexandre S Maekawa, Katherine L. Steeves, Jenna Hanrahan, André J. Simpson, Jenna Hanrahan, John‏ Kingdom, Katherine L. Steeves, Alexandre S Maekawa, Alexandre S Maekawa, Lindsay S. Cahill Alexandre S Maekawa, Karl J. Jobst, Ahmet Baschat, Katherine L. Steeves, Jenna Hanrahan, Lindsay S. Cahill John G. Sled, Grace V. Mercer, Jenna Hanrahan, Katherine L. Steeves, Grace V. Mercer, Alexandre S Maekawa, Katherine L. Steeves, John G. Sled, Jenna Hanrahan, Karl J. Jobst, Christopher K. Macgowan, Alexandre S Maekawa, Katherine L. Steeves, Jenna Hanrahan, Christopher K. Macgowan, Karl J. Jobst, Ahmet Baschat, Lindsay S. Cahill Lauren C.M. Ringer, Lauren C.M. Ringer, Lindsay S. Cahill Myrna J. Simpson, Karl J. Jobst, John‏ Kingdom, Ahmet Baschat, Christopher K. Macgowan, André J. Simpson, Lindsay S. Cahill Myrna J. Simpson, John‏ Kingdom, Ahmet Baschat, Lindsay S. Cahill Lindsay S. Cahill Lindsay S. Cahill André J. Simpson, Karl J. Jobst, Ahmet Baschat, John‏ Kingdom, André J. Simpson, Karl J. Jobst, Karl J. Jobst, John‏ Kingdom, André J. Simpson, Myrna J. Simpson, Myrna J. Simpson, André J. Simpson, Lindsay S. Cahill Karl J. Jobst, Myrna J. Simpson, Karl J. Jobst, Karl J. Jobst, Christopher K. Macgowan, Karl J. Jobst, Myrna J. Simpson, Christopher K. Macgowan, André J. Simpson, John G. Sled, John G. Sled, Lindsay S. Cahill Lindsay S. Cahill Ahmet Baschat, Karl J. Jobst, Karl J. Jobst, Lindsay S. Cahill Lindsay S. Cahill John‏ Kingdom, John G. Sled, Karl J. Jobst, Lindsay S. Cahill

Summary

Pregnant mice exposed to polystyrene micro- and nanoplastics in drinking water showed signs of placental dysfunction, with nanoplastics causing more severe effects than microplastics. Both sizes triggered a brain-sparing response in fetuses, where blood flow is redirected to protect the brain from low oxygen, a sign of fetal distress. These findings suggest that nanoplastic exposure during pregnancy could disrupt normal placental function and potentially affect fetal brain development.

Polymers
Models
Study Type Environmental

Maternal exposure to microplastics and nanoplastics has been shown to result in fetal growth restriction in mice. In this study, we investigated the placental and fetal hemodynamic responses to plastics exposure in mice using high-frequency ultrasound. Healthy, pregnant CD-1 dams were given either 106 ng/L of 5 μm polystyrene microplastics or 106 ng/L of 50 nm polystyrene nanoplastics in drinking water throughout gestation and were compared with controls. Maternal exposure to both microplastics and nanoplastics resulted in evidence of placental dysfunction that was highly dependent on the particle size. The umbilical artery blood flow increased by 48% in the microplastic-exposed group and decreased by 25% in the nanoplastic-exposed group compared to controls (p < 0.05). The microplastic- and nanoplastic-exposed fetuses showed a significant decrease in the middle cerebral artery pulsatility index of 10% and 13%, respectively, compared to controls (p < 0.05), indicating vasodilation of the cerebral circulation, a fetal adaptation that is part of the brain sparing response to preserve oxygen delivery. Hemodynamic markers of placental dysfunction and fetal hypoxia were more pronounced in the group exposed to polystyrene nanoplastics, suggesting nanoplastic exposure during human pregnancy has the potential to disrupt fetal brain development, which in turn may cause suboptimal neurodevelopmental outcomes.

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