Low dose of fine particulate matter (PM2.5) can induce acute oxidative stress, inflammation and pulmonary impairment in healthy mice

• Published in: Inhalation toxicology 2011-04, Vol.23 (5), p.257-267
• Main Authors: Riva, D.R., Magalhães, C.B., Lopes, A.A., Lanças, T., Mauad, T., Malm, O., Valença, S.S., Saldiva, P.H., Faffe, D.S., Zin, W.A.
• Format: Article
• Language: English
• Subjects: Animals; Cities; Dose-Response Relationship, Drug; Glutathione Disulfide - metabolism; Lung - drug effects; Lung - metabolism; Lung - pathology; lung injury; Lung Injury - chemically induced; Lung Injury - metabolism; Lung Injury - physiopathology; Male; Mice; Mice, Inbred BALB C; oxidative stress; Oxidative Stress - drug effects; Oxidoreductases - metabolism; Particle Size; Particulate matter; Particulate Matter - chemistry; Particulate Matter - toxicity; PM2.5; Respiratory Function Tests; respiratory mechanics
• ISSN: 0895-8378; 1091-7691
• DOI: 10.3109/08958378.2011.566290

Air pollution is associated with morbidity and mortality induced by respiratory diseases. However, the mechanisms therein involved are not yet fully clarified. Thus, we tested the hypothesis that a single acute exposure to low doses of fine particulate matter (PM2.5) may induce functional and histological lung changes and unchain inflammatory and oxidative stress processes. PM2.5 was collected from the urban area of São Paulo city during 24 h and underwent analysis for elements and polycyclic aromatic hydrocarbon contents. Forty-six male BALB/c mice received intranasal instillation of 30 μL of saline (CTRL) or PM2.5 at 5 or 15 μg in 30 μL of saline (P5 and P15, respectively). Twenty-four hours later, lung mechanics were determined. Lungs were then prepared for histological and biochemical analysis. P15 group showed significantly increased lung impedance and alveolar collapse, as well as lung tissue inflammation, oxidative stress and damage. P5 presented values between CTRL and P15: higher mechanical impedance and inflammation than CTRL, but lower inflammation and oxidative stress than P15. In conclusion, acute exposure to low doses of fine PM induced lung inflammation, oxidative stress and worsened lung impedance and histology in a dose-dependent pattern in mice.