Airway irritation, inflammation, and toxicity in mice following inhalation of metal oxide nanoparticles

Abstract

<p>Metal oxide nanoparticles are used in a broad range of industrial processes and workers may be exposed to aerosols of the particles both during production and handling. Despite the widespread use of these particles, relatively few studies have been performed to investigate the toxicological effects in the airways following inhalation. In the present study, the acute (24 h) and persistent (13 weeks) effects in the airways after a single exposure to metal oxide nanoparticles were studied using a murine inhalation model. Mice were exposed 60 min to aerosols of either ZnO, TiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub> or CeO<sub>2</sub> and the deposited doses in the upper and lower respiratory tracts were calculated. Endpoints were acute airway irritation, pulmonary inflammation based on analyses of bronchoalveolar lavage (BAL) cell composition, DNA damage assessed by the comet assay and pulmonary toxicity assessed by protein level in BAL fluid and histology. All studied particles reduced the tidal volume in a concentration-dependent manner accompanied with an increase in the respiratory rate. In addition, ZnO and TiO<sub>2</sub> induced nasal irritation. BAL cell analyses revealed both neutrophilic and lymphocytic inflammation 24-h post-exposure to all particles except TiO<sub>2</sub>. The ranking of potency regarding induction of acute lung inflammation was Al<sub>2</sub>O<sub>3</sub> = TiO<sub>2 </sub><<sub> </sub>CeO<sub>2</sub> ≪ ZnO. Exposure to CeO<sub>2</sub> gave rise to a more persistent inflammation; both neutrophilic and lymphocytic inflammation was seen 13 weeks after exposure. As the only particles, ZnO caused a significant toxic effect in the airways while TiO<sub>2</sub> gave rise to DNA-strand break as shown by the comet assay.</p

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Last time updated on 12/02/2018

This paper was published in FigShare.

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