Nickel oxide nanoparticles are highly toxic to SH-SY5Y neuronal cells. (September 2017)
- Record Type:
- Journal Article
- Title:
- Nickel oxide nanoparticles are highly toxic to SH-SY5Y neuronal cells. (September 2017)
- Main Title:
- Nickel oxide nanoparticles are highly toxic to SH-SY5Y neuronal cells
- Authors:
- Abudayyak, Mahmoud
Guzel, Elif
Özhan, Gül - Abstract:
- Abstract: Nickel oxide nanoparticles (NiO-NPs) are used in many industrial sectors including printing inks, ceramics and catalysts, and electrical and electronics industry because of their magnetic and optical properties. However, there has been still a serious lack of information about their toxicity at the cellular and molecular levels on nervous system. For that, we aimed to investigate the in vitro toxic potentials of NiO-NPs in neuronal (SH-SY5Y) cells. The particle characterisation, cellular uptake and morphological changes were determined using Transmission Electron Microscopy, dynamic light scattering and Inductively Coupled Plasma-Mass Spectrometry. Then, the cytotoxicity was evaluated by MTT and neutral red uptake assays, the genotoxicity by comet assay, the oxidative potentials by the determination of malondialdehyde, 8-hydroxy deoxyguanosine, protein carbonyl, and glutathione levels with Enzyme-Linked Immune Sorbent Assays, and the apoptotic potentials by Annexin V-FITC apoptosis detection assay with propidium iodide. According to the results, it was observed that NiO-NPs (15.0 nm ± 4.2–38.1 nm); (i) were taken up by the cells in concentration dependent manner, (ii) caused 50% inhibition in cell viability at ≥229.34 μg/mL, (iii) induced some morphological changes, (iv) induced dose-dependent DNA damage (3.2–11.0 fold) and apoptosis (80–99%), (v) significantly induced oxidative damage. In conclusion, our results support the hypothesis that NiO-NPs affect humanAbstract: Nickel oxide nanoparticles (NiO-NPs) are used in many industrial sectors including printing inks, ceramics and catalysts, and electrical and electronics industry because of their magnetic and optical properties. However, there has been still a serious lack of information about their toxicity at the cellular and molecular levels on nervous system. For that, we aimed to investigate the in vitro toxic potentials of NiO-NPs in neuronal (SH-SY5Y) cells. The particle characterisation, cellular uptake and morphological changes were determined using Transmission Electron Microscopy, dynamic light scattering and Inductively Coupled Plasma-Mass Spectrometry. Then, the cytotoxicity was evaluated by MTT and neutral red uptake assays, the genotoxicity by comet assay, the oxidative potentials by the determination of malondialdehyde, 8-hydroxy deoxyguanosine, protein carbonyl, and glutathione levels with Enzyme-Linked Immune Sorbent Assays, and the apoptotic potentials by Annexin V-FITC apoptosis detection assay with propidium iodide. According to the results, it was observed that NiO-NPs (15.0 nm ± 4.2–38.1 nm); (i) were taken up by the cells in concentration dependent manner, (ii) caused 50% inhibition in cell viability at ≥229.34 μg/mL, (iii) induced some morphological changes, (iv) induced dose-dependent DNA damage (3.2–11.0 fold) and apoptosis (80–99%), (v) significantly induced oxidative damage. In conclusion, our results support the hypothesis that NiO-NPs affect human health especially neuronal system negatively and should raise the concern about the safety associated with their applications in consumer products. … (more)
- Is Part Of:
- Neurochemistry international. Volume 108(2017)
- Journal:
- Neurochemistry international
- Issue:
- Volume 108(2017)
- Issue Display:
- Volume 108, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 108
- Issue:
- 2017
- Issue Sort Value:
- 2017-0108-2017-0000
- Page Start:
- 7
- Page End:
- 14
- Publication Date:
- 2017-09
- Subjects:
- Nickel oxide nanoparticles -- Neurotoxicity -- Genotoxicity -- Oxidative stress -- Apoptosis
Neurochemistry -- Periodicals
Neurochemistry -- Periodicals
Neurochimie -- Périodiques
Neurochemistry
Periodicals
612.804205 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01970186 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuint.2017.01.017 ↗
- Languages:
- English
- ISSNs:
- 0197-0186
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.317000
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