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Effects of polystyrene micro- and nanoplastics on androgen- and estrogen receptor activity and steroidogenesis in vitro
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Researchers tested how polystyrene micro and nanoplastics of various sizes affect hormone receptor activity and steroid hormone production in human cells grown in the lab. Smaller nanoplastics (50-1000 nm) were taken up into cells and interfered with both estrogen and androgen receptor signaling, while also altering the production of key hormones. This study provides direct evidence that nanoplastics can disrupt the human endocrine system at the cellular level, which could have implications for reproductive health.
While many plastic additives show endocrine disrupting properties, this has not been studied for micro- and nanoplastics (MNPs) particles despite their ubiquitous presence in humans. The objective of this study was to determine the effects of various sizes and concentrations of polystyrene (PS)-MNPs (50-10,000 nm, 0.01-100 μg/mL) on estrogen- and androgen receptor (ER and AR) activity and steroidogenesis in vitro. Fluorescent (F)PS-MNPs of ≤1000 nm were internalized in VM7 and H295R cells and FPS-MNPs ≤200 nm in AR-ecoscreen cells. H295R cells displayed the highest uptake and particles were closer to the nucleus than other cell types. None of the sizes and concentrations PS-MNPs tested affected ER or AR activity. In H295R cells, PS-MNPs caused some statistically significant changes in hormone levels, though these showed no apparent concentration or size-dependent patterns. Additionally, PS-MNPs caused a decrease in estriol (E3) with a maximum of 37.5 % (100 μg/mL, 50 nm) and an increase in gene expression of oxidative stress markers GPX1 (1.26-fold) and SOD1 (1.23-fold). Taken together, our data show limited endocrine-disrupting properties of PS-MNPs in vitro. Nevertheless the importance of E3 in the placenta warrants further studies in the potential effects of MNPs during pregnancy.
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Researchers exposed mouse Leydig cells to carboxylated polystyrene nanoplastics and found that testosterone production was suppressed at all tested concentrations — including doses too low to affect cell viability — while higher doses also reduced metabolic activity, suggesting endocrine disruption as a primary mode of toxicity.
Limited passage and functional effects of polystyrene micro- and nanoplastics in a physiologically-relevant in vitro human placental co-culture model
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Researchers developed a placental co-culture model to study how polystyrene micro- and nanoplastics cross the placental barrier. The study found that smaller nanoplastics (50 nm) crossed more readily than larger particles, and while most cellular functions remained unaffected, exposure to the smallest nanoplastics caused a 17% decrease in estradiol hormone levels, suggesting potential endocrine effects.
Nanoplastics Impair GnRH Neuron Migration and Neuroendocrine Function: Emerging Players in the Pathogenesis of Reproductive Disorders
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Researchers found that polystyrene nanoplastics can enter reproductive hormone-producing neurons and disrupt their function, impairing both hormone secretion and cell migration in laboratory models. The study also identified genetic variants in nanoplastic-affected genes in patients with reproductive hormone deficiency, suggesting that nanoplastics may act as endocrine disruptors contributing to reproductive disorders.
Exposure of the human placental primary cells to nanoplastics induces cytotoxic effects, an inflammatory response and endocrine disruption
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Scientists exposed human placental cells to polystyrene nanoparticles at concentrations found in human blood and observed cell death, inflammation, and disrupted hormone production, with smaller 20-nanometer particles causing more damage than larger ones. This is significant because the placenta is the critical barrier protecting developing babies, and these findings suggest nanoplastics may interfere with pregnancy hormones and placental function at real-world exposure levels.
Effects of polystyrene nanoplastics on the female reproductive system in mice: Implications for ovarian function and follicular development
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Researchers exposed female mice to polystyrene nanoplastics orally for 29 days and examined the effects on their reproductive systems. They found that nanoplastic exposure disrupted estrous cycles, impaired follicle development, and altered hormone levels in a dose-dependent manner. The study suggests that nanoplastics, due to their extremely small size, may cross biological barriers and accumulate in reproductive tissues, raising concerns about potential effects on fertility.
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