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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 Nanoplastics Reproductive & Development Sign in to save

Exposure to Polystyrene Nanoplastics Compromise Ovarian Reserve Function and Endometrial Decidualization in Early Pregnant Mice

Journal of Applied Toxicology 2025 9 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.
J. Li, Qian‐Feng Qiao, Qian‐Feng Qiao, J. Li, Liqing Wang, Liqing Wang, Qiongjun Xu, Qiongjun Xu, Qiongjun Xu, Qiongjun Xu, Xiaomei Wu, Xiaomei Wu, J. Li, Qi‐Duo Chen, Qi‐Duo Chen, Tao‐Yu Sheng, Tao‐Yu Sheng, Qian‐Feng Qiao, Man‐Xue Cui, Qian‐Feng Qiao, Man‐Xue Cui, J. Li, J. Li, Xuehong Pang, Yongjiang Zhou Yongjiang Zhou

Summary

Female mice exposed to polystyrene nanoplastics for 90 days before pregnancy had fewer successful pregnancies, smaller pups, and damaged ovaries with reduced egg counts. The nanoplastics disrupted key reproductive hormones and interfered with the uterine process needed for embryo implantation. This study raises concerns that nanoplastic exposure through food and water could harm female fertility and pregnancy outcomes in humans.

Polymers
Body Systems
Models

In the environment, nanoplastics (NPs) have been shown to adversely impact reproductive health, yet research on their effects during early pregnancy is scarce. This study investigated the impact of NPs on endometrial decidualization in early pregnant mice and fertility. Female mice were administered polystyrene nanoplastics (PS-NPs) orally for 90 days before pregnancy. Our findings indicated that PS-NPs exposure decreased the live birth rate and neonatal crown-rump length. Decreased embryo implantation sites and uterine wet weight were observed post PS-NPs exposure. Histological examination revealed structural defects in the uteri of early pregnant mice and a significant reduction in follicular count across all stages in the PS-NPs-treated groups. Serum levels of estradiol (E<sub>2</sub>) and progesterone (P) were elevated, while follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels were diminished post-exposure. Additionally, PS-NPs exposure upregulated the expression of the endometrial decidualization marker HOXA10 in uterine decidua. In conclusion, our results suggest that exposure to PS-NPs may disrupt endometrial decidualization during early pregnancy. This disruption is likely due to the perturbation of hormonal balance within the hypothalamic-pituitary-ovary including FSH, LH, E<sub>2</sub>, and P levels. These hormonal alterations may arrest follicular development, consequently leading to detrimental pregnancy outcomes and compromised neonatal birth conditions. Our study provided a new perspective on understanding the possible effects of microplastics on female fertility.

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