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Microplastic particles cause intestinal damage and other adverse effects in zebrafish Danio rerio and nematode Caenorhabditis elegans

  • Lili Lei
  • , Siyu Wu
  • , Shibo Lu
  • , Mengting Liu
  • , Yang Song
  • , Zhenhuan Fu
  • , Huahong Shi
  • , Kathleen M. Raley-Susman
  • , Defu He*
  • *此作品的通讯作者
  • East China Normal University
  • Vassar College

科研成果: 期刊稿件文章同行评审

摘要

Microplastics have been frequently detected in aquatic environments, and there are increasing concerns about potential effects on biota. In this study, zebrafish Danio rerio and nematode Caenorhabditis elegans were used as model organisms for microplastic exposure in freshwater pelagic (i.e. water column) and benthic (i.e. sediment) environments. We investigated the toxic effects of five common types of microplastics: polyamides (PA), polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC) and polystyrene (PS) particles. Results showed no or low lethality in D. rerio after exposure for 10 d at 0.001–10.0 mg L− 1 microplastics. The PA, PE, PP and/or PVC microplastics with ~ 70 μm size caused intestinal damage including cracking of villi and splitting of enterocytes. Exposure to 5.0 mg m− 2 microplastics for 2 d significantly inhibited survival rates, body length and reproduction of C. elegans. Moreover, exposure to microplastics reduced calcium levels but increased expression of the glutathione S-transferase 4 enzyme in the intestine, which indicates intestinal damage and oxidative stress are major effects of microplastic exposure. Among 0.1, 1.0 and 5.0 μm sizes of fluorescently labeled PS, 1.0 μm particles caused the highest lethality, the maximum accumulation, the lowest Ca2 + level in the intestine and the highest expression of glutathione S-transferase 4 in nematodes. Taken together, these findings suggest that intestinal damage is a key effect of microplastics; and that the toxicity of microplastics is closely dependent on their size, rather than their composition.

源语言英语
页(从-至)1-8
页数8
期刊Science of the Total Environment
619-620
DOI
出版状态已出版 - 1 4月 2018
已对外发布

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