Developmental toxicity of penconazole in Zebrfish (Danio rerio) embryos

Penconazole is a widely used fungicide that is toxic to a variety of organisms including fish. In the present study, we investigated the developmental toxicity of penconazole on zebrafish embryos by exposing to different concentrations of penconazole (0.8, 1.6 and 2.4 mg/L) from 4-h post-fertilizati...

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Bibliographic Details
Published inChemosphere (Oxford) Vol. 200; pp. 8 - 15
Main Authors Icoglu Aksakal, Feyza, Ciltas, Abdulkadir
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.06.2018
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Summary:Penconazole is a widely used fungicide that is toxic to a variety of organisms including fish. In the present study, we investigated the developmental toxicity of penconazole on zebrafish embryos by exposing to different concentrations of penconazole (0.8, 1.6 and 2.4 mg/L) from 4-h post-fertilization (hpf). Hatching, survival, and heart rates, body length, malformation and expression of several genes were detected. The results showed that penconazole exposure induced developmental toxicity, including delayed hatching, reduced survival, and heart rate. In addition to this, exposure to penconazole caused malformations, including pericardial edema, yolk sac edema, axial malformation, tail malformation and spinal curvature. Furthermore, RT-PCR results showed that mRNA levels of antioxidant genes were down-regulated after penconazole exposure. On the other hand, mRNA levels of interleukin 1 beta and interferon in embryos were up-regulated after exposure to penconazole. In summary, our data indicated that penconazole cause embryonic development toxicity on zebrafish embryos. •Penconazole induced developmental toxicity in zebrafish embryos.•Penconazole inhibited the survival rate and hatching rate of zebrafish embryos.•Exposure to penconazole caused several developmental abnormalities in zebrafish embryos.•Penconazole at 0.8–2.4 mg/L altered the mRNA levels of some oxidative stress and immune related genes.
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2018.02.094