Tuning the inflammatory response to silver nanoparticles via quercetin in Caco-2 (co-)cultures as model of the human intestinal mucosa

Martirosyan, Alina;Grintzalis, Konstantinos;Polet, Madeleine;Laloux, Laurie;Schneider, Yves-Jacques
(2016) Toxicology Letters — Vol. 253, p. 36-45 (2016)

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Authors
  • Martirosyan, AlinaUCLouvain
    Author
  • Grintzalis, KonstantinosUCLouvain
    Author
  • Polet, MadeleineUCLouvain
    Author
  • Laloux, LaurieUCLouvain
    Author
  • Schneider, Yves-JacquesUCLouvain
    Author
Abstract
Interaction of nanoparticles with food matrix components may cause unpredictable health complications. Using an improved Caco-2 cell-based in vitro (co-)culture model the potential of quercetin as one of the major food flavonoids to alter the effect of silver nanoparticles (Ag-NPs) <20 nm in the human intestinal mucosa at real life concentrations was investigated. Ag-NPs (15–90 mg/ml) decreased cell viability and reduced thiol groups, induced oxidative/nitrosative stress and lipid peroxidation and led to activity changes of various antioxidant enzymes after 3 h exposure. The contribution of Ag+ ions within the concentrations released from nanoparticles was shown to be less important, compared to Ag-NPs. While leading to inflammatory response in the intestines, Ag-NPs, paradoxically, also showed a potential anti-infammatory effect manifested in down-regulated IL-8 levels. Quercetin, co-administered with Ag-NPs, led to a reduction of cytotoxicity, oxidative stress, and recovered metabolic activity of Caco-2 cells, suggesting the protective effects of this flavonoid against the harmful effect of Ag-NPs. Quercetin not only alleviated the effect of Ag-NPs on the gastrointestinal cells, but also demonstrated a potential to serve as a tool for reversible modulation of intestinal permeability.
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Citations

Martirosyan, A., Grintzalis, K., Polet, M., Laloux, L., & Schneider, Y.-J. (2016). Tuning the inflammatory response to silver nanoparticles via quercetin in Caco-2 (co-)cultures as model of the human intestinal mucosa. Toxicology Letters, 253, 36-45. https://doi.org/10.1016/j.toxlet.2016.04.018 (Original work published 2016)