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Pulmonary inflammation and tumor induction in lung tumor susceptible A/J and resistant C57BL/6J mice exposed to welding fume

Authors :
Reynolds Steven H
Roberts Jenny R
Erdely Aaron
Young Shih-Houng
Battelli Lori A
Kashon Michael L
Zeidler-Erdely Patti C
Antonini James M
Source :
Particle and Fibre Toxicology, Vol 5, Iss 1, p 12 (2008)
Publication Year :
2008
Publisher :
BMC, 2008.

Abstract

Abstract Background Welding fume has been categorized as "possibly carcinogenic" to humans. Our objectives were to characterize the lung response to carcinogenic and non-carcinogenic metal-containing welding fumes and to determine if these fumes caused increased lung tumorigenicity in A/J mice, a lung tumor susceptible strain. We exposed male A/J and C57BL/6J, a lung tumor resistant strain, by pharyngeal aspiration four times (once every 3 days) to 85 μg of gas metal arc-mild steel (GMA-MS), GMA-stainless steel (SS), or manual metal arc-SS (MMA-SS) fume, or to 25.5 μg soluble hexavalent chromium (S-Cr). Shams were exposed to saline vehicle. Bronchoalveolar lavage (BAL) was done at 2, 7, and 28 days post-exposure. For the lung tumor study, gross tumor counts and histopathological changes were assessed in A/J mice at 48 and 78 weeks post-exposure. Results BAL revealed notable strain-dependent differences with regards to the degree and resolution of the inflammatory response after exposure to the fumes. At 48 weeks, carcinogenic metal-containing GMA-SS fume caused the greatest increase in tumor multiplicity and incidence, but this was not different from sham. By 78 weeks, tumor incidence in the GMA-SS group versus sham approached significance (p = 0.057). A significant increase in perivascular/peribronchial lymphoid infiltrates for the GMA-SS group versus sham and an increased persistence of this fume in lung cells compared to the other welding fumes was found. Conclusion The increased persistence of GMA-SS fume in combination with its metal composition may trigger a chronic, but mild, inflammatory state in the lung possibly enhancing tumorigenesis in this susceptible mouse strain.

Details

Language :
English
ISSN :
17438977
Volume :
5
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Particle and Fibre Toxicology
Publication Type :
Academic Journal
Accession number :
edsdoj.362db125d842a99540d456a95a7324
Document Type :
article
Full Text :
https://doi.org/10.1186/1743-8977-5-12