Pulmonary toxicity following acute coexposures to diesel particulate matter and α-quartz crystalline silica in the Sprague-Dawley rat. (7th June 2017)

• Record Type: Journal Article
• Authors: Farris, Breanne Y.; Antonini, James M.; Fedan, Jeffrey S.; Mercer, Robert R.; Roach, Katherine A.; Chen, Bean T.; Schwegler-Berry, Diane; Kashon, Michael L.; Barger, Mark W.; Roberts, Jenny R.
• Is Part Of: Inhalation toxicology. Volume 29:Number 7(2017)
• Page Start: 322
• Page End: 339
• Publication Date: 2017-06-07
• Subjects: Crystalline silica -- diesel exhaust particulate matter -- immune response -- occupational exposure -- pulmonary fibrosis; Pulmonary toxicology -- Animal models -- Periodicals; Pulmonary toxicology -- Periodicals; Air -- Pollution -- Health aspects -- Periodicals; 616.200471
• DOI: 10.1080/08958378.2017.1361487
• Languages: English
• ISSNs: 0895-8378

Abstract

Abstract: The effects of acute pulmonary coexposures to silica and diesel particulate matter (DPM), which may occur in various mining operations, were investigated in vivo . Rats were exposed by intratracheal instillation (IT) to silica (50 or 233 µg), DPM (7.89 or 50 µg) or silica and DPM combined in phosphate-buffered saline (PBS) or to PBS alone (control). At one day, one week, one month, two months and three months postexposure bronchoalveolar lavage and histopathology were performed to assess lung injury, inflammation and immune response. While higher doses of silica caused inflammation and injury at all time points, DPM exposure alone did not. DPM (50 µg) combined with silica (233 µg) increased inflammation at one week and one-month postexposure and caused an increase in the incidence of fibrosis at one month compared with exposure to silica alone. To assess susceptibility to lung infection following coexposure, rats were exposed by IT to 233 µg silica, 50 µg DPM, a combination of the two or PBS control one week before intratracheal inoculation with 5 × 10 5 Listeria monocytogenes . At 1, 3, 5, 7 and 14 days following infection, pulmonary immune response and bacterial clearance from the lung were evaluated. Coexposure to DPM and silica did not alter bacterial clearance from the lung compared to control. Although DPM and silica coexposure did not alter pulmonary susceptibility to infection in this model, the study showed that noninflammatory doses of DPM had the capacity to increase silica-induced lung injury, inflammation and onset/incidence of fibrosis.