Microplastics and nanoplastics co-exposure modulates chromium bioaccumulation and physiological responses in ratsShow others and affiliations
2025 (English)In: Environment International, ISSN 0160-4120, E-ISSN 1873-6750, Vol. 198, article id 109421Article in journal (Refereed) Published
Abstract [en]
The environmental fragmentation of plastics generates a mixture of plastic particles of various sizes, which frequently co-occur with other mobile and persistent environmental pollutants. Despite the prevalence of such scenarios, the interaction between micro- and nanoplastics (MNPs) and their combined effects with environmental pollutants, such as highly toxic hexavalent chromium (Cr(VI)), remain almost entirely unexplored in mammalian species. This study demonstrated that nanoplastic and microplastic particles co-aggregate and together influence Cr bioaccumulation patterns and related physiological alterations in rats. Following a four-week repeated intragastric exposure of Wistar rats to MNPs and Cr(VI), either alone or in combination, MNPs significantly enhanced Cr bioaccumulation in the liver, heart, brain, and skin. Under co-exposure conditions, Cr(VI) was the primary driver of cellular effects observed in the blood, including shifts in immune cell subpopulations (e.g., neutrophils, lymphocytes) and alterations in red blood cell indices, while serum biochemistry reflected limited physiological stress. MNPs per se decreased creatine kinase activity and increased cholesterol levels. In summary, polystyrene MNPs increase Cr(VI) distribution and bioavailability, but co-exposure does not uniformly exacerbate toxicity. Instead, their interaction may selectively alter physiological responses, emphasizing the need for a deeper understanding of their combined effects and potential health risks.
Place, publisher, year, edition, pages
Elsevier, 2025. Vol. 198, article id 109421
Keywords [en]
Polystyrene particles, Heavy metals, Mixture toxicity, Liver, Brain
National Category
Environmental Sciences
Identifiers
URN: urn:nbn:se:oru:diva-120353DOI: 10.1016/j.envint.2025.109421ISI: 001460484400001Scopus ID: 2-s2.0-105001261838OAI: oai:DiVA.org:oru-120353DiVA, id: diva2:1949213
Funder
Knowledge Foundation, 20160019; 20220122, 20230020; 20200017
Note
This work was supported by the Swedish Knowledge Foundation [Grants No. 20160019; 20220122, 20230020]. We acknowledge scientific support from the Exploring Inflammation in Health and Disease (X-HiDE) Consortium, which is a strategic research profile at Örebro University funded by the Knowledge Foundation [Grant No. 20200017].
2025-04-022025-04-022025-04-15Bibliographically approved