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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 Human Health Effects Marine & Wildlife Nanoplastics Reproductive & Development Sign in to save

Developmental toxicity and mechanism of polychlorinated biphenyls 126 and nano-polystyrene combined exposure to zebrafish larvae

Ecotoxicology and Environmental Safety 2024 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Yao Hu, Fang‐Hong Nie, Min Zhang, Qing-Lang Song, Wan Wei, Guang-Zhou Lv, Yun-Li Wei, Danju Kang, Zhibao Chen, Hong‐Ying Lin, Jinjun Chen

Summary

Researchers exposed zebrafish embryos to a combination of a toxic industrial chemical (PCB126) and nanoplastics and found that the mixture caused more severe developmental problems than either pollutant alone. The nanoplastics appeared to increase the absorption and toxic effects of PCB126, leading to greater heart defects and developmental abnormalities. The study suggests that nanoplastics may worsen the impact of existing chemical pollutants on aquatic life.

Polymers
Body Systems
Study Type In vivo

3,3',4,4',5-Pentachlorobiphenyl (PCB126) is the most toxic congener of dioxin-like polychlorinated biphenyls (DL PCBs), while nanoplastics (NPs) have recently emerged as significant marine pollutants, both posing threats to aquatic organisms and human health. They coexist in the environment, but their comprehensive toxicological effects remain unclear. In this study, zebrafish embryos were simultaneously exposed to PCB126 and 80-nanometer nanoplastyrene (NPS). Researchers utilized fluorescence microscopy, qPCR, histopathological examination, and transcriptomic sequencing to investigate the developmental toxicity of different concentrations of PCB126 and NPS individually or in combination on zebrafish embryos and larvae. Results indicate that the chorion significantly impedes the accumulation of NPS (p < 0.05). It is noteworthy that this barrier effect diminishes upon simultaneous exposure to PCB126. In this experiment, the semi-lethal concentration of PCB126 for larvae was determined to be 6.33 μg/L. Exposure to PCB126 induces various deformities, primarily mediated through the aryl hydrocarbon receptor (AHR). Similarly, exposure to NPS also activates AHR, leading to developmental impairments. Furthermore, transcriptomic sequencing revealed similar effects of PCB126 and NPS on the gene expression trends in zebrafish larvae, but combined exposure to both exacerbates the risk of cancer and induces more severe cardiac toxicity. At this level, co-exposure to PCB126 and NPS adversely affects the development of zebrafish larvae. This study contributes to a deeper understanding of the in vivo accumulation of DL polychlorinated biphenyls and microplastics in actual aquatic environments and their impact on fish development.

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