Oxidative Stress and Genotoxicity of Zinc Oxide Nanoparticles to Pseudomonas Species, Human Promyelocytic Leukemic (HL-60), and Blood Cells
Autor: | Deepa Gandhi, Deepika Soni, R.A. Pandey, Prashant Tarale, Amit Bafana, Saravanadevi Sivanesan |
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Rok vydání: | 2017 |
Předmět: |
DNA damage
Endocrinology Diabetes and Metabolism Clinical Biochemistry HL-60 Cells 02 engineering and technology 010501 environmental sciences Biology medicine.disease_cause 01 natural sciences Biochemistry Inorganic Chemistry Pseudomonas medicine Humans Viability assay Cytotoxicity 0105 earth and related environmental sciences chemistry.chemical_classification Reactive oxygen species Biochemistry (medical) General Medicine 021001 nanoscience & nanotechnology Molecular biology Anti-Bacterial Agents Comet assay Oxidative Stress chemistry Leukocytes Mononuclear Nanoparticles DNA fragmentation Zinc Oxide 0210 nano-technology Oxidative stress Genotoxicity DNA Damage |
Zdroj: | Biological Trace Element Research. 178:218-227 |
ISSN: | 1559-0720 0163-4984 |
DOI: | 10.1007/s12011-016-0921-y |
Popis: | In the present study, toxicity of commercial zinc oxide nanoparticles (ZnO NPs) was studied on the bacterium Pseudomonas sp., human promyelocytic leukemia (HL-60) cells, and peripheral blood mononuclear cells (PBMC). The toxicity was assessed by measuring growth, cell viability, and protein expression in bacterial cell. The bacterial growth and viability decreased with increasing concentrations of ZnO NP. Three major proteins, ribosomal protein L1 and L9 along with alkyl hydroperoxides reductase, were upregulated by 1.5-, 1.7-, and 2.0-fold, respectively, after ZnO NP exposure. The results indicated oxidative stress as the leading cause of toxic effect in bacteria. In HL-60 cells, cytotoxic and genotoxic effects along with antioxidant enzyme activity and reactive oxygen species (ROS) generation were studied upon ZnO NP treatment. ZnO NP exhibited dose-dependent increase in cell death after 24-h exposure. The DNA-damaging potential of ZnO NP in HL-60 cells was maximum at 0.05 mg/L concentration. Comet assay showed 70-80% increase in tail DNA at 0.025 to 0.05 mg/L ZnO NP concentration. A significant increase of 1.6-, 1.4-, and 2.0-fold in ROS level was observed after 12 h. Genotoxic potential of ZnO NPs was also demonstrated in PBMC through DNA fragmentation. Thus, ZnO NP, besides being an essential element having antibacterial activity, also showed toxicity towards human cells (HL-60 and PBMC). |
Databáze: | OpenAIRE |
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