PMID- 21840035 OWN - NLM STAT- MEDLINE DCOM- 20120222 LR - 20131121 IS - 1879-1298 (Electronic) IS - 0045-6535 (Linking) VI - 85 IP - 6 DP - 2011 Oct TI - Developmental toxicity of cypermethrin in embryo-larval stages of zebrafish. PG - 1010-6 LID - 10.1016/j.chemosphere.2011.07.024 [doi] AB - 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 mug L(-)(1)) until 96 h. Among a suite of morphological abnormalities, the unique phenotype curvature was observed at concentrations as low as 25 mug L(-)(1). Studies revealed that 400 mug 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 mug 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. CI - Crown Copyright (c) 2011. Published by Elsevier Ltd. All rights reserved. FAU - Shi, Xiangguo AU - Shi X AD - State Key Laboratory of Reproductive Medicine, Institute of Toxicology, Nanjing Medical University, Nanjing 210029, China. FAU - Gu, Aihua AU - Gu A FAU - Ji, Guixiang AU - Ji G FAU - Li, Yuan AU - Li Y FAU - Di, Jing AU - Di J FAU - Jin, Jing AU - Jin J FAU - Hu, Fan AU - Hu F FAU - Long, Yan AU - Long Y FAU - Xia, Yankai AU - Xia Y FAU - Lu, Chuncheng AU - Lu C FAU - Song, Ling AU - Song L FAU - Wang, Shoulin AU - Wang S FAU - Wang, Xinru AU - Wang X LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110812 PL - England TA - Chemosphere JT - Chemosphere JID - 0320657 RN - 0 (Antioxidants) RN - 0 (Pesticide Residues) RN - 0 (Pyrethrins) RN - 0 (RNA, Messenger) RN - 059QF0KO0R (Water) RN - 1TR49121NP (cypermethrin) RN - 4Y8F71G49Q (Malondialdehyde) RN - EC 3.4.22.- (Caspase 3) SB - IM MH - Animals MH - Antioxidants/metabolism MH - Apoptosis/drug effects MH - Caspase 3/metabolism MH - DNA Repair/drug effects MH - Embryo, Nonmammalian/cytology/*drug effects/enzymology/metabolism MH - Endpoint Determination MH - Larva/cytology/drug effects/genetics/metabolism MH - Lipid Peroxidation/drug effects MH - Malondialdehyde/metabolism MH - Oxidation-Reduction MH - Pesticide Residues/*toxicity MH - Pyrethrins/*toxicity MH - RNA, Messenger/genetics/metabolism MH - Toxicity Tests, Acute/*methods MH - Transcriptome/drug effects MH - Water/chemistry MH - Zebrafish/*embryology/genetics/metabolism EDAT- 2011/08/16 06:00 MHDA- 2012/02/23 06:00 CRDT- 2011/08/16 06:00 PHST- 2011/03/06 00:00 [received] PHST- 2011/06/27 00:00 [revised] PHST- 2011/07/18 00:00 [accepted] PHST- 2011/08/16 06:00 [entrez] PHST- 2011/08/16 06:00 [pubmed] PHST- 2012/02/23 06:00 [medline] AID - S0045-6535(11)00860-5 [pii] AID - 10.1016/j.chemosphere.2011.07.024 [doi] PST - ppublish SO - Chemosphere. 2011 Oct;85(6):1010-6. doi: 10.1016/j.chemosphere.2011.07.024. Epub 2011 Aug 12.