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Micro-sized polyethylene particles affect cell viability and oxidative stress responses in human colorectal adenocarcinoma Caco-2 and HT-29 cells
被引:32
作者:
Herrala, Mikko
[1
]
Huovinen, Marjo
[1
]
Jarvela, Essi
[1
]
Hellman, Julia
[1
]
Tolonen, Pauliina
[1
]
Lahtela-Kakkonen, Maija
[1
]
Rysa, Jaana
[1
]
机构:
[1] Univ Eastern Finland, Sch Pharm, Kuopio, Finland
关键词:
Polyethylene;
Microplastics;
Toxicity;
In vitro;
Reactive oxygen species;
Ethanol-extraction;
IN-VITRO TOXICITY;
MICROPLASTICS;
CHEMICALS;
LEAD;
D O I:
10.1016/j.scitotenv.2023.161512
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Plastic isa widely utilized material and polyethylene is one of the most used plastic types. Microplastics are plastic par-ticles (size <5 mm) which are primarily a micro-size range or results from degeneration of larger plastic pieces in the environment. Drinking water and food are two main human exposure sources for microplastics and consequently ef-fects of microplastics in gastrointestinal tract are considered important. Still, only little is known how microplastics and plastic associated chemicals affect the human health. The aim of our study was to evaluate the ability of micro-sized polyethylene to cause harmful effects in human intestinal cells. Raw ultra-high molecular-weight polyethylene (size 5-60 mu m) was used. In addition, polyethylene particles were extracted with ethanol to determine the effect of ex-traction process on toxicity of the particles. In the experiments, human colorectal adenocarcinoma Caco-2 and HT-29 cells were exposed to polyethylene (0.25-1.0 mg/ml) or extracts for 48 h. After exposure, cell viability and cytotoxicity were assessed with MTT and lactate dehydrogenase assay. Reactive oxygen species (ROS) production was measured with dichlorofluorescin diacetate and cytoplasmic production of superoxide with dihydroethidium and mitochondrial superoxide production with MitoSOX. The 48-h exposure to polyethylene decreased dose-dependently cell viability and increased oxidative stress, especially mitochondrial superoxide production, in both cell lines. Effects on ROS or cy-tosolic superoxide production were not observed. Also, exposure to extracts decreased cell viability and increased ox-idative stress in cell cultures, but there were differences between cell lines. These effects were most probably caused by the remaining particles rather than the compounds released from the plastic during the extraction. In conclusion, our study shows that micro-sized polyethylene and ethanol-extracted polyethylene in high concentrations decreased cell viability and increased oxidative stress responses in intestinal cells. These results contribute to the existing evidence on potential adverse human health effects of microplastics.
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