Polystyrene micro- and nanoplastics cause placental dysfunction in mice

Author:

Dibbon Katherine C1,Mercer Grace V1,Maekawa Alexandre S1,Hanrahan Jenna1,Steeves Katherine L1,Ringer Lauren C M1,Simpson André J2,Simpson Myrna J2,Baschat Ahmet A34,Kingdom John C567,Macgowan Christopher K89,Sled John G58910,Jobst Karl J1,Cahill Lindsay S111

Affiliation:

1. Department of Chemistry, Memorial University of Newfoundland , St. John’s, Newfoundland and Labrador , Canada

2. Environmental NMR Centre and Department of Physical and Environmental Sciences, University of Toronto , Toronto, Ontario , Canada

3. Department of Gynecology & Obstetrics , Johns Hopkins Center for Fetal Therapy, , Baltimore, MD , USA

4. Johns Hopkins University , Johns Hopkins Center for Fetal Therapy, , Baltimore, MD , USA

5. Department of Obstetrics and Gynaecology, University of Toronto , Toronto, Ontario , Canada

6. Maternal-Fetal Medicine Division , Department of Obstetrics and Gynaecology, , Toronto, Ontario , Canada

7. Mount Sinai Hospital , Department of Obstetrics and Gynaecology, , Toronto, Ontario , Canada

8. Translational Medicine, Hospital for Sick Children , Toronto, Ontario, Canada

9. Department of Medical Biophysics, University of Toronto , Toronto, Ontario , Canada

10. Mouse Imaging Centre, Hospital for Sick Children , Toronto, Ontario, Canada

11. Discipline of Radiology, Memorial University of Newfoundland , St. John’s, Newfoundland and Labrador , Canada

Abstract

Abstract 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.

Funder

Government of Canada’s New Frontiers in Research Fund

Canadian Foundation for Innovation

Newfoundland and Labrador Department of Industry, Energy and Technology

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,General Medicine,Reproductive Medicine

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