Figures & data
TABLE 1 Concentrations of welding fume sample (mg/instillate)
FIG. 1 Pulmonary clearance of bacteria by rats pre-exposed to (A) 2 mg of manual metal arc, stainless steel (MMA-SS) welding fume or (B) 0.82 mg insoluble Fe2O3, 0.60 mg soluble Cr2Na2O7, or 0.06 mg insoluble NiO alone or in combination. The MMA-SS and metal samples were intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means in Log10 base units ± standard error of measurement (n = 4–12); *significantly greater than corresponding saline control at each timepoint (p < 0.05).
![FIG. 1 Pulmonary clearance of bacteria by rats pre-exposed to (A) 2 mg of manual metal arc, stainless steel (MMA-SS) welding fume or (B) 0.82 mg insoluble Fe2O3, 0.60 mg soluble Cr2Na2O7, or 0.06 mg insoluble NiO alone or in combination. The MMA-SS and metal samples were intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means in Log10 base units ± standard error of measurement (n = 4–12); *significantly greater than corresponding saline control at each timepoint (p < 0.05).](/cms/asset/8a18e562-4371-413c-8392-0125664c3a26/iimt_a_233589_uf0001_b.gif)
FIG. 2 Percent change in body weight of rats pre-exposed to (A) 2 mg of manual metal arc, stainless steel (MMA-SS) welding fume or (B) 0.82 mg insoluble Fe2O3, 0.60 mg soluble Cr2Na2O7, or 0.06 mg insoluble NiO alone or in combination. The MMA-SS and metal samples were intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–12); *significantly reduced than corresponding saline control at each time point (p < 0.05).
![FIG. 2 Percent change in body weight of rats pre-exposed to (A) 2 mg of manual metal arc, stainless steel (MMA-SS) welding fume or (B) 0.82 mg insoluble Fe2O3, 0.60 mg soluble Cr2Na2O7, or 0.06 mg insoluble NiO alone or in combination. The MMA-SS and metal samples were intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–12); *significantly reduced than corresponding saline control at each time point (p < 0.05).](/cms/asset/15f8f02f-99ef-4948-8cf1-54050fcfbf80/iimt_a_233589_uf0002_b.gif)
TABLE 2 Lung inflammation and injury
FIG. 3 Zymosan-stimulated chemiluminescence of macrophages recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled three days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly greater than corresponding saline control at Day 6 (p < 0.05).
![FIG. 3 Zymosan-stimulated chemiluminescence of macrophages recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled three days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly greater than corresponding saline control at Day 6 (p < 0.05).](/cms/asset/f991ead4-97ab-4960-a3af-b3ce93a8886c/iimt_a_233589_uf0003_b.gif)
FIG. 4 TNFα measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly less than corresponding saline control at Days 3 and 6 (p < 0.05).
![FIG. 4 TNFα measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly less than corresponding saline control at Days 3 and 6 (p < 0.05).](/cms/asset/ae0d52b8-2aca-46d3-8e5d-f5fddfbcee14/iimt_a_233589_uf0004_b.gif)
FIG. 5 IL-6 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly greater than corresponding saline control at Days 3 and 6 (p < 0.05); n.d. = not detected.
![FIG. 5 IL-6 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly greater than corresponding saline control at Days 3 and 6 (p < 0.05); n.d. = not detected.](/cms/asset/3a60ed9b-6e68-4a70-a97c-b365a7bfdde2/iimt_a_233589_uf0005_b.gif)
FIG. 6 IL-10 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7).
![FIG. 6 IL-10 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7).](/cms/asset/b0aac8bf-29f8-4019-9e5c-cbe8d5668d3d/iimt_a_233589_uf0006_b.gif)
FIG. 7 IL-2 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled three days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly less than corresponding saline control at Days 3 and 6 (p < 0.05).
![FIG. 7 IL-2 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled three days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly less than corresponding saline control at Days 3 and 6 (p < 0.05).](/cms/asset/89613dbe-5d5d-475b-b8c7-d154042f9f34/iimt_a_233589_uf0007_b.gif)
FIG. 8 IL-12p70 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly greater than corresponding saline control at Day 6 (p < 0.05).
![FIG. 8 IL-12p70 measured within the bronchoalveolar lavage fluid (BALF) recovered from rats pre-exposed to 0.60 mg soluble Cr2Na2O7. The Cr sample was intratracheally instilled 3 days prior to intratracheal inoculation with 5 × 103 L. monocytogenes. Control animals were pretreated with saline. Values are means ± standard error of measurement (n = 4–7); *significantly greater than corresponding saline control at Day 6 (p < 0.05).](/cms/asset/841e3b27-41ba-4895-9566-149d3dd98377/iimt_a_233589_uf0008_b.gif)