Table 1.
Effect of NFκB inhibitors (and control drugs) on endothelial TF expression in the NYIDD sickle mouse*
| Condition or Agent | n | TF expression (%) | P# |
|---|---|---|---|
| NY1DD at ambient air | 10 | 12.8 ± 2.9 | |
| NY1DD post-HR | 27 | 34.7 ± 6.3 | <0.001 |
| + andrographolide | 6 | 18.0 ± 2.1 | <0.001 |
| + curcumin | 10 | 23.2 ± 7.3 | <0.001 |
| + didox | 6 | 14.3 ± 2.3 | <0.001 |
| + trimidox | 12 | 17.5 ±6.9 | <0.001 |
| + isohelenin | 5 | 10.8 ± 3.0 | <0.001 |
| + sulfasalazine | 5 | 25.2 ± 3.0 | <0.05 |
| + salsalate | 6 | 29.3 ± 5.7 | ns |
| + 4H-andrographolide§ | 6 | 31.3 ±2.1 | ns |
| + hydroxyurea§ | 6 | 35.6 ± 4.8 | ns |
TF is expressed as percentage of pulmonary veins being TF positive, and data are shown as mean ± SD.
Post-H/R is compared to ambient air; all others are compared to post-HR with vehicle but without the active drug.
These agents are control drugs; all others are known NFκB inhibitors.