0
Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Human Health Effects Reproductive & Development Sign in to save

Maternal exposure to polystyrene microplastics alters placental metabolism in mice

Metabolomics 2022 81 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.
Zahra Aghaei, Zahra Aghaei, Grace V. Mercer, Myrna J. Simpson, Paul A. Helm, Paul A. Helm, Grace V. Mercer, Grace V. Mercer, Paul A. Helm, Paul A. Helm, Grace V. Mercer, Paul A. Helm, Paul A. Helm, Paul A. Helm, Grace V. Mercer, Paul A. Helm, Paul A. Helm, Grace V. Mercer, Grace V. Mercer, Grace V. Mercer, Paul A. Helm, John G. Sled, Paul A. Helm, Lindsay S. Cahill Lindsay S. Cahill Paul A. Helm, Paul A. Helm, Paul A. Helm, Paul A. Helm, Paul A. Helm, John‏ Kingdom, André J. Simpson, C. Schneider, Paul A. Helm, Grace V. Mercer, Ahmet Baschat, John G. Sled, Paul A. Helm, Grace V. Mercer, Karl J. Jobst, Paul A. Helm, C. Schneider, Paul A. Helm, Paul A. Helm, Lindsay S. Cahill Paul A. Helm, Paul A. Helm, Karl J. Jobst, Zahra Aghaei, Paul A. Helm, Paul A. Helm, Christopher K. Macgowan, Paul A. Helm, John G. Sled, Paul A. Helm, Ahmet Baschat, Lindsay S. Cahill Karl J. Jobst, Christopher K. Macgowan, Zahra Aghaei, André J. Simpson, Myrna J. Simpson, John‏ Kingdom, Christopher K. Macgowan, Ahmet Baschat, Lindsay S. Cahill Karl J. Jobst, John‏ Kingdom, Lindsay S. Cahill Paul A. Helm, Lindsay S. Cahill Lindsay S. Cahill Ahmet Baschat, Myrna J. Simpson, Lindsay S. Cahill Paul A. Helm, André J. Simpson, Karl J. Jobst, Karl J. Jobst, Paul A. Helm, Karl J. Jobst, Paul A. Helm, Ahmet Baschat, John‏ Kingdom, André J. Simpson, André J. Simpson, André J. Simpson, Myrna J. Simpson, John‏ Kingdom, Myrna J. Simpson, Karl J. Jobst, Lindsay S. Cahill Myrna J. Simpson, Myrna J. Simpson, Karl J. Jobst, Christopher K. Macgowan, Karl J. Jobst, Karl J. Jobst, Paul A. Helm, John G. Sled, Lindsay S. Cahill Lindsay S. Cahill André J. Simpson, John G. Sled, Christopher K. Macgowan, Karl J. Jobst, Karl J. Jobst, Ahmet Baschat, Lindsay S. Cahill John‏ Kingdom, Lindsay S. Cahill Paul A. Helm, John G. Sled, Karl J. Jobst, Paul A. Helm, Lindsay S. Cahill

Summary

Researchers exposed pregnant mice to polystyrene microplastics and examined how placental metabolism was affected. The study found significant changes in placental metabolic pathways that could help explain the fetal growth restriction previously observed in microplastic-exposed pregnancies. These findings suggest that microplastic exposure during pregnancy may interfere with the placenta's ability to support normal fetal development.

Polymers
Body Systems
Models
Study Type Environmental

INTRODUCTION: The rapid growth in the worldwide use of plastics has resulted in a vast accumulation of microplastics in the air, soil and water. The impact of these microplastics on pregnancy and fetal development remains largely unknown. In pregnant mice, we recently demonstrated that exposure to micro- and nanoplastics throughout gestation resulted in significant fetal growth restriction. One possible explanation for reduced fetal growth is abnormal placental metabolism. OBJECTIVES: To evaluate the effect of maternal exposure to microplastics on placental metabolism. METHODS: In the present study, CD-1 pregnant mice were exposed to 5 μm polystyrene microplastics in filtered drinking water at one of four concentrations (0 ng/L (controls), 10 ng/L, 10 ng/L, 10 ng/L) throughout gestation (n = 7-11/group). At embryonic day 17.5, placental tissue samples were collected (n = 28-44/group). Metabolite profiles were determined using  H high-resolution magic angle spinning magnetic resonance spectroscopy. RESULTS: The relative concentration of lysine (p = 0.003) and glucose (p < 0.0001) in the placenta were found to decrease with increasing microplastic concentrations, with a significant reduction at the highest exposure concentration. Multivariate analysis identified shifts in the metabolic profile with MP exposure and pathway analysis identified perturbations in the biotin metabolism, lysine degradation, and glycolysis/gluconeogenesis pathways. CONCLUSION: Maternal exposure to microplastics resulted in significant alterations in placental metabolism. This study highlights the potential impact of microplastic exposure on pregnancy outcomes and that efforts should be made to minimize exposure to plastics, particularly during pregnancy.

Sign in to start a discussion.

Share this paper