Developmental toxicity of cypermethrin in embryo-larval stages of zebrafish

  • Xiangguo Shi
  • , Aihua Gu
  • , Guixiang Ji
  • , Yuan Li
  • , Jing Di
  • , Jing Jin
  • , Fan Hu
  • , Yan Long
  • , Yankai Xia
  • , Chuncheng Lu
  • , Ling Song
  • , Shoulin Wang
  • , Xinru Wang

Research output: Contribution to journalArticlepeer-review

145 Scopus citations

Abstract

Cypermethrin, a type II pyrethroid insecticide, is widely used throughout the world in agriculture, forestry, horticulture and homes. Though the neurotoxicity of cypermethrin has been thoroughly studied in adult rodents, little is so far available regarding the developmental toxicity of cypermethrin to fish in early life stages. To explore the potential developmental toxicity of cypermethrin, 4-h post-fertilization (hpf) zebrafish embryos were exposed to various concentrations of cypermethrin (0, 25, 50, 100, 200 and 400μgL-1) until 96h. Among a suite of morphological abnormalities, the unique phenotype curvature was observed at concentrations as low as 25μgL-1. Studies revealed that 400μgL-1 cypermethrin significantly increased malondialdehyde production. In addition, activity of antioxidative enzymes including superoxide dismutase and catalase were significantly induced in zebrafish larvae in a concentration-dependent manner. To further investigate the toxic effects of cypermethrin on fish, acridine orange (AO) staining was performed at 400μgL-1 cypermethrin and the result showed notable signs of apoptosis mainly in the nervous system. Cypermethrin also down-regulated ogg1 and increased p53 gene expression as well as the caspase-3 activity. Our results demonstrate that cypermethrin was able to induce oxidative stress and produce apoptosis through the involvement of caspases in zebrafish embryos. In this study, we investigated the developmental toxicity of cypermethrin using zebrafish embryos, which could be helpful in fully understanding the potential mechanisms of cypermethrin exposure during embryogenesis and also suggested that zebrafish could serve as an ideal model for studying developmental toxicity of environmental contaminants.

Original languageEnglish (US)
Pages (from-to)1010-1016
Number of pages7
JournalChemosphere
Volume85
Issue number6
DOIs
StatePublished - Oct 2011

All Science Journal Classification (ASJC) codes

  • Environmental Engineering
  • Environmental Chemistry
  • General Chemistry
  • Pollution
  • Public Health, Environmental and Occupational Health
  • Health, Toxicology and Mutagenesis

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