4.7 Article

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

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 896, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2023.165214

Keywords

Water flea; Polystyrene plastics; PPCPs; Enhanced toxicity; Simultaneous exposure

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In this study, the combined toxic effects of simultaneous exposure to microplastics and triclosan on Daphnia magna were investigated. It was found that simultaneous exposure resulted in increased mortality and altered antioxidant enzymatic activities compared to single exposure to triclosan. The accumulation of triclosan was also observed due to the inhibition of the multixenobiotic resistance activity by microplastics. These findings suggest the synergistic toxic effects of simultaneous exposure to microplastics and triclosan.
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 & mu;m 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 MPsexposed 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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