Challenge | Compound | Dose | n | Cell Number (×104/animal) | |
---|---|---|---|---|---|
Total Cells | Eosinophils | ||||
mg/kg | |||||
Pretreatment | |||||
Saline | 6 | 10.9 ± 2.7 | 1.4 ± 0.4 | ||
Antigen | Vehicle | 12 | 60.2 ± 9.03-167 | 38.4 ± 6.63-167 | |
S-5751 | 1 | 9 | 36.0 ± 6.73-150 | 22.0 ± 4.7 | |
3 | 10 | 24.9 ± 5.53-160 | 14.0 ± 3.63-160 | ||
10 | 12 | 17.5 ± 3.73-160 | 8.9 ± 2.03-160 | ||
Saline | 5 | 6.8 ± 1.2 | 1.1 ± 0.2 | ||
Antigen | Vehicle | 11 | 22.4 ± 4.53-159 | 13.4 ± 3.53-159 | |
BW A868C | 1 | 11 | 9.1 ± 2.23-150 | 3.8 ± 1.03-150 | |
Post-treatment | |||||
Saline | 8 | 4.1 ± 1.0 | 0.4 ± 0.1 | ||
Antigen | Vehicle | 8 | 54.5 ± 11.03-167 | 34.1 ± 7.43-167 | |
S-5751 | 1 | 8 | 27.7 ± 4.03-150 | 15.8 ± 2.43-160 | |
3 | 8 | 19.1 ± 2.53-160 | 8.1 ± 1.53-160 | ||
10 | 8 | 12.1 ± 2.93-160 | 5.7 ± 1.63-160 |
Nasal lavage was performed 5 h after the last antigen challenge. S-5751 was orally administered 1 h before antigen challenge and BW A868C was intravenously given 10 min before challenge. In the study for investigating the inhibitory action of post-treatment with S-5751 on inflammatory cell infiltration, S-5751 was administered 2 h after the antigen challenge.