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April 7, 2026International Journal of Molecular Sciences4 citationsOpen Access

Micro- and Nanoplastics as Disruptors of Digestive and Hepatopancreatic Homeostasis: Insights into the Plastic-Gut-Liver Axis

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NCNicoletta CapuanoMLMartina LombardiNCNoemi Cafà

Key Points

  • The review aims to explore how micro- and nanoplastics affect gastrointestinal and liver homeostasis and their underlying mechanisms.
  • Critical examination of existing literature on micro- and nanoplastics.
  • Analysis of primary exposure routes, including ingestion and inhalation.
  • Discussion of mechanisms affecting intestinal integrity and liver function.
  • Highlighting multi-organ interactions and dysbiosis propagation.
  • Micro- and nanoplastics compromise intestinal barrier integrity and induce oxidative stress.
  • Dysbiosis and inflammatory signaling are linked to metabolic reprogramming and insulin resistance.
  • Emerging evidence indicates pancreatic dysfunction due to micro- and nanoplastics exposure.
  • Human evidence is limited, highlighting a need for more standardized research approaches.

Abstract

Micro- and nanoplastics (MPs/NPs) have emerged as pervasive environmental contaminants with increasing implications for human health, particularly within the digestive system. This review critically examines the role of MPs/NPs as disruptors of gastrointestinal and liver homeostasis through the lens of the plastic–gut–liver axis. We synthesize current evidence on primary exposure routes—including ingestion, inhalation, dermal contact, and transplacental transfer—and highlight their intestinal uptake, systemic dissemination, and tissue accumulation. Mechanistically, MPs/NPs compromise intestinal barrier integrity, promote oxidative stress, and induce microbiota dysbiosis, facilitating the translocation of microbial-derived signals to the liver via the portal circulation. This process triggers inflammatory signaling cascades, metabolic reprogramming, and immune dysregulation, contributing to hepatic steatosis, insulin resistance, and potential carcinogenic processes. Emerging evidence also implicates pancreatic dysfunction and β-cell stress within a broader gut–liver axis context. We further discuss the systemic propagation of MPs/NPs-induced dysbiosis along multi-organ axes, including gut–lung and gut–brain interactions. Despite robust preclinical data, human evidence remains limited due to methodological heterogeneity and the lack of standardized biomarkers. This review underscores critical knowledge gaps and emphasizes the need for integrative, translational approaches to clarify long-term health risks and inform regulatory strategies within the environmental exposome framework.

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Cite This Study

Capuano et al. (2026) studied this question.

synapsesocial.com/papers/69d49fe5b33cc4c35a228551https://doi.org/10.3390/ijms27073272
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