4.7 Article

Presence of Titanium and Toxic Effects Observed in Rat Lungs, Kidneys, and Central Nervous System in vivo and in Cultured Astrocytes in vitro on on Exposure by Titanium Dioxide Nanorods

Journal

INTERNATIONAL JOURNAL OF NANOMEDICINE
Volume 15, Issue -, Pages 9939-9960

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S275937

Keywords

apoptosis; nanoparticles; neuro-functional changes; tissue damage; toxicity

Funding

  1. National Research, Development and Innovation Office-NKFIH [GINOP-2.3.2-15 -2016 -00038, EFOP -3.6.1 -162016-00008]
  2. New National Excellence Program of the Ministry for Innovation and Technology [UNKP-19-4-SZ 1E-14, UNKP-20-5-SZTE-655]
  3. Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences [BO/00878/19/8]

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Background: Non-spherical titanium dioxide (TiO2) nanoparticles have been increasingly applied in various biomedical and technological fields. Their toxicological characterization is, however, less complete than that of roundish nanoparticles. Materials and Methods: Anatase form TiO2 nanorods, ca. 15x65 nm in size, were applied to cultured astrocytes in vitro and to the airways of young adult Wistar rats in vivo in 5, 10, and 8 mg/kg BW dose for altogether 28 days. Presence of nanorods and cellular damage was investigated in the astrocytes and in rat lungs and kidneys. Functional damage of the nervous system was studied by electrophysiological methods. Results: The treated astrocytes showed loss of viability without detectable apoptosis. In rats, TiO2 nanorods applied to the airways reached the blood and various organs including the lungs, kidneys, and the central nervous system. In lung and kidney samples, nanorods were observed within (partly damaged) phagolysosomes and attached to organelles, and apoptotic cell death was also detected. In cortical and peripheral electrophysiological activity, alterations corresponding to energy shortage (resulting possibly from mitochondria' damage) and astrocytic dysfunction were detected. Local titanium levels and relative weight of the investigated organs, apoptotic cell death in the lungs and kidneys, and changes in the central and peripheral nervous activity were mostly proportional to the applied doses, and viability loss of the cultured astrocytes was also dose-dependent, suggesting causal relationship of treatments and effects. Conclusion: Based on localization of the visualized nanorods, on neuro-functional changes, and on literature data, the toxic mechanism involved mitochondrial damage, oxidative stress, and apoptotic cell death. These indicate potential human toxicity and occupational risk in case of exposure to rod-shaped TiO2 nanoparticles.

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