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. Gut & Microbiome Human Health Effects Nanoplastics Sign in to save

Early-life exposure to polystyrene micro- and nanoplastics disrupts metabolic homeostasis and gut microbiota in juvenile mice with a size-dependent manner

The Science of The Total Environment 2024 15 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.
Hao Lu, Peng Xu, Guobing Sun, Bingxie Chen, Yuncan Zheng, Jiaqi Zhang, Guoxiu Wang

Summary

Pregnant mice given polystyrene micro or nanoplastics in their drinking water passed the particles to their pups through the placenta and breast milk, with smaller nanoplastics accumulating more heavily in organs. The nanoplastics (0.05 micrometers) caused more severe gut damage, liver dysfunction, and metabolic disruption in the young mice than the larger microplastics (5 micrometers). This study demonstrates that early-life exposure to nanoplastics, even before birth, can disrupt development in a size-dependent way, with the smallest particles posing the greatest risk.

Polymers
Models
Study Type Environmental

Early-life exposure to different sizes of micro- and nanoplastics (MNPs) affects biotoxicity, which is related not only to the dose but also directly to particle size. In this study, pregnant ICR mice received drinking water containing 5 μm polystyrene microplastics (5 μm PS-MPs) or 0.05 μm polystyrene nanoplastics (0.05 μm PS-NPs) from pregnancy to the end of lactation. Histopathological and molecular biological detection, 16s rRNA sequencing for intestinal flora analysis, and targeted metabolomics analysis were used to look into how early-life exposure to MNPs of various sizes affects young mice's growth and development, gut flora, and metabolism. The outcomes showed that 0.05 μm and 5 μm PS-MNPs can pass through the placental and mammary barriers, and MNPs accumulating in various organs were size-dependent: the greater the accumulation in organs, the smaller the particle size. Further studies found that the larger 5 μm PS-MPs caused only small accumulation in organs, with the main health hazard being the disruption of intestinal barrier and liver function, indirectly causing gut dysbiosis and metabolic disorders. In contrast, the smaller 0.05 μm PS-NPs caused excessive accumulation in organs, not only impaired the function of the intestine and liver, but also caused direct mechanical damage to physical tissues, and ultimately resulted in more severe intestinal and metabolic disorders. Our findings underline the size-dependent risks associated with micro- and nanoplastics exposure early in life and highlight the necessity for tailored approaches to address health damages from early MNPs exposure.

Sign in to start a discussion.

More Papers Like This

Article Tier 2

The role of gut microbiota in mediating increased toxicity of nano-sized polystyrene compared to micro-sized polystyrene in mice

This mouse study found that nano-sized polystyrene plastics were significantly more toxic than micro-sized ones, causing greater gut inflammation, liver damage, and metabolic disruption. The key difference was driven by how each size affected gut bacteria: nanoplastics caused a more severe shift toward harmful bacteria and away from beneficial ones. The findings suggest that the smallest plastic particles may pose the greatest health risk because they more dramatically disrupt the gut microbiome.

Article Tier 2

Polystyrene microplastics exposure: Disruption of intestinal barrier integrity and hepatic function in infant mice

Researchers found that even low concentrations of polystyrene microplastics caused significant gut barrier damage and liver injury in infant mice. The microplastics disrupted the intestinal lining, allowed particles to leak into the bloodstream, and triggered liver fat accumulation and altered gut bacteria colonization. The study raises concerns about microplastic exposure during early life, when developing digestive and liver systems may be especially vulnerable.

Article Tier 2

Polystyrene microplastics induce size-dependent multi-organ damage in mice: Insights into gut microbiota and fecal metabolites

A mouse study found that microplastics of different sizes cause damage to multiple organs, but in different ways. Smaller particles (0.5 micrometers) spread more widely through the body and caused more inflammation in the spleen, kidneys, heart, lungs, and liver, while larger particles (5 micrometers) caused worse gut damage and disrupted gut bacteria linked to brain inflammation. This suggests that the size of microplastics we are exposed to matters for which organs are most affected.

Article Tier 2

Maternal exposure to different sizes of polystyrene microplastics during gestation causes metabolic disorders in their offspring

Researchers exposed pregnant mice to polystyrene microplastics of two different sizes during gestation and examined metabolic effects in their offspring. They found that maternal microplastic exposure altered cholesterol, triglyceride levels, and amino acid metabolism in the offspring, with larger 5-micrometer particles causing more pronounced effects. The study suggests that prenatal microplastic exposure may increase the risk of metabolic disorders in the next generation.

Article Tier 2

Negative impact of oral exposure to polystyrene microplastics on glucose tolerance and intestinal environment in mice is independent of particle size

Researchers fed mice on a high-fat diet polystyrene microplastics of three different sizes and found that all sizes impaired glucose tolerance, regardless of particle dimensions. The microplastics caused intestinal inflammation, altered gut bacteria, and damaged the lining of the intestinal tract. The study suggests that the harmful metabolic effects of ingesting microplastics may occur broadly and are not limited to one particular particle size.

Share this paper