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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. Detection Methods Environmental Sources Gut & Microbiome Human Health Effects Nanoplastics Policy & Risk Reproductive & Development Sign in to save

Consequences of nano and microplastic exposure in rodent models: the known and unknown

Particle and Fibre Toxicology 2022 163 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.
Walison Augusto da Silva Brito, Fiona Mutter, Kristian Wende, Alessandra Lourenço Cecchini, Anke Schmidt, Sander Bekeschus

Summary

This review summarizes what rodent studies have revealed about the health effects of micro and nanoplastic exposure, including inflammation, oxidative stress, metabolic disruption, and reproductive harm. Researchers found that toxic effects depend heavily on particle size, polymer type, shape, and exposure route, making it difficult to draw broad conclusions. The study highlights major gaps in current knowledge and calls for more standardized research to better assess human health risks.

The ubiquitous nature of micro- (MP) and nanoplastics (NP) is a growing environmental concern. However, their potential impact on human health remains unknown. Research increasingly focused on using rodent models to understand the effects of exposure to individual plastic polymers. In vivo data showed critical exposure effects depending on particle size, polymer, shape, charge, concentration, and exposure routes. Those effects included local inflammation, oxidative stress, and metabolic disruption, leading to gastrointestinal toxicity, hepatotoxicity, reproduction disorders, and neurotoxic effects. This review distillates the current knowledge regarding rodent models exposed to MP and NP with different experimental designs assessing biodistribution, bioaccumulation, and biological responses. Rodents exposed to MP and NP showed particle accumulation in several tissues. Critical responses included local inflammation and oxidative stress, leading to microbiota dysbiosis, metabolic, hepatic, and reproductive disorders, and diseases exacerbation. Most studies used MP and NP commercially provided and doses higher than found in environmental exposure. Hence, standardized sampling techniques and improved characterization of environmental MP and NP are needed and may help in toxicity assessments of relevant particle mixtures, filling knowledge gaps in the literature.

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