Figure 1
The effect of loss of histamine signaling in particulate matter–induced thrombin generation. Fine urban particulate matter (National Institute of Standards and Technology Standard Reference Material, SRM 1649a 200 μg/mouse in 50 μL PBS) or vehicle was administered intratracheally to 20-25 g, 6-8 week old male C57BL/6 mice as previously described.4 (A) After 24 hours BAL fluid was obtained and histamine levels were measured using a commercially available assay (EIA Histamine IM2015, Beckman Coulter). (B) Mice were treated with famotidine (10 mg/kg) and desloratadine (10 mg/kg) in 150 μL of PBS 4 hours before treatment with PM followed by an additional dose of famotidine 8 hours later. Twenty-four hours after PM administration, BAL fluid was obtained and IL-6 levels were measured as previously described (ELISA).3 (C,D) H1R and H2R receptor double knockout mice (H1R−/−/H2R−/−) or littermate controls were treated with PM and 24 hours later IL-6 and TAT were measured in BAL fluid and citrated plasma as previously described.3 The protocol for the use of mice was approved by the Animal Care and Use Committee at Northwestern University. N = 4 or 5 animals for each group. *P < .05 compared with PBS control; and NS, not significant using ANOVA with Bonferroni posttest comparison.

The effect of loss of histamine signaling in particulate matter–induced thrombin generation. Fine urban particulate matter (National Institute of Standards and Technology Standard Reference Material, SRM 1649a 200 μg/mouse in 50 μL PBS) or vehicle was administered intratracheally to 20-25 g, 6-8 week old male C57BL/6 mice as previously described. (A) After 24 hours BAL fluid was obtained and histamine levels were measured using a commercially available assay (EIA Histamine IM2015, Beckman Coulter). (B) Mice were treated with famotidine (10 mg/kg) and desloratadine (10 mg/kg) in 150 μL of PBS 4 hours before treatment with PM followed by an additional dose of famotidine 8 hours later. Twenty-four hours after PM administration, BAL fluid was obtained and IL-6 levels were measured as previously described (ELISA). (C,D) H1R and H2R receptor double knockout mice (H1R−/−/H2R−/−) or littermate controls were treated with PM and 24 hours later IL-6 and TAT were measured in BAL fluid and citrated plasma as previously described. The protocol for the use of mice was approved by the Animal Care and Use Committee at Northwestern University. N = 4 or 5 animals for each group. *P < .05 compared with PBS control; and NS, not significant using ANOVA with Bonferroni posttest comparison.

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