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Lung exposure to nanoparticles modulates an asthmatic response in a mouse model
The European respiratory journal, 2011-02, Vol.37 (2), p.299
[Peer Reviewed Journal]
EISSN: 1399-3003 ;DOI: 10.1183/09031936.00168509 ;PMID: 20530043
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Title:
Lung exposure to nanoparticles modulates an asthmatic response in a mouse model
Author:
Hussain, S
;
Vanoirbeek, J A J
;
Luyts, K
;
De Vooght, V
;
Verbeken, E
;
Thomassen, L C J
;
Martens, J A
;
Dinsdale, D
;
Boland, S
;
Marano, F
;
Nemery, B
;
Hoet, P H M
Subjects:
Animals
;
Asthma - chemically induced
;
Asthma - physiopathology
;
Bronchial Hyperreactivity
;
Bronchoalveolar Lavage Fluid
;
Disease Models, Animal
;
Eosinophils
;
Gold - adverse effects
;
Immunoglobulin E - blood
;
Lung - physiopathology
;
Macrophages
;
Male
;
Mice
;
Mice, Inbred BALB C
;
Nanoparticles - adverse effects
;
Neutrophils
;
Pulmonary Edema - chemically induced
;
Pulmonary Edema - physiopathology
;
Titanium - adverse effects
;
Toluene 2,4-Diisocyanate - toxicity
Is Part Of:
The European respiratory journal, 2011-02, Vol.37 (2), p.299
Description:
The aim of this study was to investigate the modulation of an asthmatic response by titanium dioxide (TiO₂) or gold (Au) nanoparticles (NPs) in a murine model of diisocyanate-induced asthma. On days 1 and 8, BALB/c mice received 0.3% toluene diisocyanate (TDI) or the vehicle acetone-olive oil (AOO) on the dorsum of both ears (20 μL). On day 14, the mice were oropharyngeally dosed with 40 μL of a NP suspension (0.4 mg·mL⁻¹ (∼0.8 mg·kg⁻¹) TiO₂ or Au). 1 day later (day 15), the mice received an oropharyngeal challenge with 0.01% TDI (20 μL). On day 16, airway hyperreactivity (AHR), bronchoalveolar lavage (BAL) cell and cytokine analysis, lung histology, and total serum immunoglobulin E were assessed. NP exposure in sensitised mice led to a two- (TiO₂) or three-fold (Au) increase in AHR, and a three- (TiO₂) or five-fold (Au) increase in BAL total cell counts, mainly comprising neutrophils and macrophages. The NPs taken up by BAL macrophages were identified by energy dispersive X-ray spectroscopy. Histological analysis revealed increased oedema, epithelial damage and inflammation. In conclusion, these results show that a low, intrapulmonary doses of TiO₂ or Au NPs can aggravate pulmonary inflammation and AHR in a mouse model of diisocyanate-induced asthma.
Publisher:
England
Language:
English
Identifier:
EISSN: 1399-3003
DOI: 10.1183/09031936.00168509
PMID: 20530043
Source:
MEDLINE
Alma/SFX Local Collection
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