4.7 Article

Developmental toxicity of cypermethrin in embryo-larval stages of zebrafish

Journal

CHEMOSPHERE
Volume 85, Issue 6, Pages 1010-1016

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2011.07.024

Keywords

Cypermethrin; Developmental toxicity; Zebrafish; Oxidative stress

Funding

  1. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  2. National Basic Research Program of China (973 Program) [2009CB941703]
  3. National Science Foundation of China [30901210]
  4. Natural Science Foundation of Jiangsu Province [BK2009422]
  5. Natural Science Foundation of the Jiangsu Higher Education Institutions of China [09KJB330002]
  6. Ministry of Education of China [20093234120001]

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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 400 mu g L-1) until 96 h. Among a suite of morphological abnormalities, the unique phenotype curvature was observed at concentrations as low as 25 mu g L-1. Studies revealed that 400 mu g L-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 400 mu g L-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. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.

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