2017
DOI: 10.1016/j.jhazmat.2016.12.040
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Chronic exposure of zinc oxide nanoparticles causes deviant phenotype in Drosophila melanogaster

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Cited by 48 publications
(24 citation statements)
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“…Exposure to various types of nanoparticles (Ag, TiO 2 , Co, Au, ZnO, zirconia, and hydroxyapatite nanoparticles) is known to cause aberrant phenotypes with aberration observed in the wings, bristles, thorax, abdomen, eyes, cuticle development, and pigmentation 36 . While some of these aberrations are caused by mutations and are passed down onto successive generations 35,37 not all of them are inheritable. In a Drosophila model, nanoparticles can also cause somatic mutations 38,39 , induce alteration in a signaling pathway 40 resulting in a defective adult fly 36 , or cause developmental abnormalities 41,42 , any of which may be responsible for the aberrations observed.…”
Section: Discussionmentioning
confidence: 99%
“…Exposure to various types of nanoparticles (Ag, TiO 2 , Co, Au, ZnO, zirconia, and hydroxyapatite nanoparticles) is known to cause aberrant phenotypes with aberration observed in the wings, bristles, thorax, abdomen, eyes, cuticle development, and pigmentation 36 . While some of these aberrations are caused by mutations and are passed down onto successive generations 35,37 not all of them are inheritable. In a Drosophila model, nanoparticles can also cause somatic mutations 38,39 , induce alteration in a signaling pathway 40 resulting in a defective adult fly 36 , or cause developmental abnormalities 41,42 , any of which may be responsible for the aberrations observed.…”
Section: Discussionmentioning
confidence: 99%
“…Increased oxidative load with increasing concentration of ZnO NPs clearly indicates towards oxidative stress triggered by these NPs. In addition, this study has clearly shown that ZnO NPs cause phenotypic abnormalities, which might be transmitted to the progeny, while no phenotypic abnormality was reported in parent flies [18]. The genotoxic potential of ZnO NPs has been demonstrated in ovary cells of Chinese hamsters, by chromosome aberration test [19], in a human epidermal cell line [20], in primary human epidermal keratinocytes [21] and in human liver cells [22] by comet assay and in the human carcinoma cell line by comet and micronucleus assays [23].…”
Section: Discussionmentioning
confidence: 63%
“…Toxicity of ENMs has been observed in multiple animal models. For example, compared to control, decreased viability and transgenerational toxicity have been observed in D. melanogaster after ingestion of various ENMs (Anand et al, 2017;Raj et al, 2017), genotoxicity and increase in reactive oxygen species (ROS) in C. elegans (Gonzalez-Moragas et al, 2017;Kong et al, 2017;Rogers et al, 2015), and genotoxicity, developmental toxicity, and lung injury in rodents (Duke et al, 2017;Ho et al, 2017;Rahman et al, 2017;Wan et al, 2017;. A challenge in developing toxicity profiles is that novel ENMs can be developed quickly; therefore, ENM toxicity profiling must include predictive models that can link ENM characteristics with their toxicity.…”
Section: Introductionmentioning
confidence: 99%