Surface area- and mass-based comparison of fine and ultrafine nickel oxide lung toxicity and augmentation of allergic response in an ovalbumin asthma model

Background: The correlation of physico-chemical properties with mechanisms of toxicity has been proposed as an approach to predict the toxic potential of the vast number of emerging nanomaterials. Although relationships have been established between properties and the acute pulmonary inflammation in...

Full description

Saved in:
Bibliographic Details
Published in:Inhalation toxicology 2019-07, Vol.31 (8), p.299-324
Main Authors: Roach, Katherine A., Anderson, Stacey E., Stefaniak, Aleksandr B., Shane, Hillary L., Kodali, Vamsi, Kashon, Michael, Roberts, Jenny R.
Format: Article
Language:English
Subjects:
Animals
Asthma - chemically induced
Bronchoalveolar Lavage Fluid - chemistry
Bronchoalveolar Lavage Fluid - cytology
Cytokines - immunology
Female
hypersensitivity
Hypersensitivity - physiopathology
immune response
Immunoglobulin E - blood
Immunophenotyping
Lung - drug effects
Lung - physiopathology
Lymphocytes - immunology
Mice
Mice, Inbred BALB C
Nanotoxicology
Nickel - toxicity
nickel oxide nanoparticles
Ovalbumin
ovalbumin allergy model
Particle Size
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background: The correlation of physico-chemical properties with mechanisms of toxicity has been proposed as an approach to predict the toxic potential of the vast number of emerging nanomaterials. Although relationships have been established between properties and the acute pulmonary inflammation induced by nanomaterials, properties' effects on other responses, such as exacerbation of respiratory allergy, have been less frequently explored. Methods: In this study, the role of nickel oxide (NiO) physico-chemical properties in the modulation of ovalbumin (OVA) allergy was examined in a murine model. Results: 181 nm fine (NiO-F) and 42 nm ultrafine (NiO-UF) particles were characterized and incorporated into a time course study where measured markers of pulmonary injury and inflammation were associated with NiO particle surface area. In the OVA model, exposure to NiO, irrespective of any metric was associated with elevated circulating total IgE levels. Serum and lung cytokine levels were similar with respect to NiO surface area. The lower surface area was associated with an enhanced Th2 profile, whereas the higher surface area was associated with a Th1-dominant profile. Surface area-normalized groups also exhibited similar alterations in OVA-specific IgE levels and lung neutrophil number. However, lung eosinophil number and allergen challenge-induced alterations in lung function related more to particle size, wherein NiO-F was associated with an increased enhanced pause response and NiO-UF was associated with increased lung eosinophil burden. Conclusions: Collectively, these findings suggest that although NiO surface area correlates best with acute pulmonary injury and inflammation following respiratory exposure, other physico-chemical properties may contribute to the modulation of immune responses in the lung.
ISSN:0895-8378
1091-7691
DOI:10.1080/08958378.2019.1680775