Oxidative stress induced by pure and iron-doped amorphous silica nanoparticles in subtoxic conditions.

Napierska, Dorota;Rabolli, Virginie;Thomassen, Leen C J;Dinsdale, David;Hoet, Peter H;et.al.
(2012) Chemical Research in Toxicology — Vol. 25, n° 4, p. 828-837 (2012)

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Authors
  • Napierska, DorotaKUL
    Author
  • Rabolli, VirginieUCLouvain
    Author
  • Thomassen, Leen C JKUL
    Author
  • Dinsdale, David
    Author
  • Lison, Dominiqueorcid-logoUCLouvain
    Author
  • Hoet, Peter H
    Author
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Abstract
Amorphous silica nanoparticles (SiO₂-NPs) have found broad applications in industry and are currently intensively studied for potential uses in medical and biomedical fields. Several studies have reported cytotoxic and inflammatory responses induced by SiO₂-NPs in different cell types. The present study was designed to examine the association of oxidative stress markers with SiO₂-NP induced cytotoxicity in human endothelial cells. We used pure monodisperse amorphous silica nanoparticles of two sizes (16 and 60 nm; S16 and S60) and a positive control, iron-doped nanosilica (16 nm; SFe), to study the generation of hydroxyl radicals (HO·) in cellular-free conditions and oxidative stress in cellular systems. We investigated whether SiO₂-NPs could influence intracellular reduced glutathione (GSH) and oxidized glutathione (GSSG) levels, increase lipid peroxidation (malondialdehyde (MDA) and 4-hydroxyalkenal (HAE) concentrations), and up-regulate heme oxygenase-1 (HO-1) mRNA expression in the studied cells. None of the particles, except SFe, produced ROS in cell-free systems. We found significant modifications for all parameters in cells treated with SFe nanoparticles. At cytotoxic doses of S16 (40-50 μg/mL), we detected weak alterations of intracellular glutathione (4 h) and a marked induction of HO-1 mRNA (6 h). Cytotoxic doses of S60 elicited similar responses. Preincubation of cells being exposed to SiO₂-NPs with an antioxidant (5 mM N-acetylcysteine, NAC) significantly reduced the cytotoxic activity of S16 and SFe (when exposed up to 25 and 50 μg/mL, respectively) but did not protect cells treated with S60. Preincubation with NAC significantly reduced HO-1 mRNA expression in cells treated with SFe but did not have any effect on HO-1 mRNA level in cell exposed to S16 and S60. Our study demonstrates that the chemical composition of the silica nanoparticles is a dominant factor in inducing oxidative stress.
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Citations

Napierska, D., Rabolli, V., Thomassen, L. C. J., Dinsdale, D., Princen, C., Gonzalez, L., Poels, K. L. C., Kirsch-Volders, M., Lison, D., Martens, J. A., & Hoet, P. H. (2012). Oxidative stress induced by pure and iron-doped amorphous silica nanoparticles in subtoxic conditions. Chemical Research in Toxicology, 25(4), 828-837. https://doi.org/10.1021/tx200361v (Original work published 2012)