Titanium Dioxide Nanoparticles Modulate Systemic Immune Response and Increase Levels of Reduced Glutathione in Mice after Seven-Week Inhalation

. 2023 Feb 18 ; 13 (4) : . [epub] 20230218

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid36839135

Grantová podpora
No. 214547-2 European Commission
No. P503/12/G147 the Czech Science Foundation
P503/20/02203S Czech Science Foundation
COOPERATIO/LF1 Charles University
the Czech MEYS: LM2018121 RECETOX
the Czech MEYS: CZ.02.1.01/0.0/0.0/15_003/0000469 CETOCOEN PLUS
the Czech MEYS: CZ.02.1.01/0.0/0.0/17_043/0009632 CETOCOEN Excellence
No 857560 European Union's Horizon
RECOOP Research Centers Cedars - Sinai Medical Center's International Research and Innovation in Medicine Program

Titanium dioxide nanoparticles (TiO2 NPs) are used in a wide range of applications. Although inhalation of NPs is one of the most important toxicologically relevant routes, experimental studies on potential harmful effects of TiO2 NPs using a whole-body inhalation chamber model are rare. In this study, the profile of lymphocyte markers, functional immunoassays, and antioxidant defense markers were analyzed to evaluate the potential adverse effects of seven-week inhalation exposure to two different concentrations of TiO2 NPs (0.00167 and 0.1308 mg TiO2/m3) in mice. A dose-dependent effect of TiO2 NPs on innate immunity was evident in the form of stimulated phagocytic activity of monocytes in low-dose mice and suppressed secretory function of monocytes (IL-18) in high-dose animals. The effect of TiO2 NPs on adaptive immunity, manifested in the spleen by a decrease in the percentage of T-cells, a reduction in T-helper cells, and a dose-dependent decrease in lymphocyte cytokine production, may indicate immunosuppression in exposed mice. The dose-dependent increase in GSH concentration and GSH/GSSG ratio in whole blood demonstrated stimulated antioxidant defense against oxidative stress induced by TiO2 NP exposure.

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