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Synergistic toxic mechanisms of microplastics and triclosan via multixenobiotic resistance (MXR) inhibition–mediated autophagy in the freshwater water flea Daphnia magna

The Science of The Total Environment 2023 30 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.
Jin-Sol Lee, Yunmoon Oh, Hae Eun Park, Jae‐Seong Lee, Jae-Seong Lee, Hyung Sik Kim, Hyung Sik Kim

Summary

Researchers exposed water fleas to microplastics and triclosan, a common antimicrobial chemical, and found that the combination was more toxic than either pollutant alone. Microplastics interfered with the organisms' natural defense system for expelling foreign chemicals, allowing triclosan to accumulate and trigger harmful autophagy. This suggests that microplastics may amplify the toxicity of other environmental contaminants in aquatic ecosystems.

Models
Study Type In vivo

Since a mixed state of environmental contaminants, including microplastics (MPs), heavy metals, pharmaceuticals, and personal care products (PPCPs), exists in aquatic ecosystems, it is necessary to evaluate not only the adverse effects of exposure to a single stressor but to combined stressors. In this study, we exposed the freshwater water flea Daphnia magna to 2 μm MPs and triclosan (TCS), one of PPCPs, for 48 h to investigate the synergistic toxic consequences of simultaneous exposure to both pollutants. We measured in vivo endpoints, antioxidant responses, multixenobiotic resistance (MXR) activity, and autophagy-related protein expression via the PI3K/Akt/mTOR and MAPK signaling pathways. While MPs single exposure did not show toxic effects in water fleas, simultaneous exposure to TCS and MPs was associated with significantly greater deleterious effects in the form of increased mortality and alterations in antioxidant enzymatic activities compared with water fleas exposed to TCS alone. In addition, MXR inhibition was confirmed by measurement of the expression of P-glycoproteins and multidrug-resistance proteins in MPs-exposed groups, which led to the accumulation of TCS. Overall, these results suggest that simultaneous exposure to MPs and TCS resulted in higher TCS accumulation via MXR inhibition, leading to synergistic toxic effects such as autophagy in D. magna.

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