Table 1.
Treatment | Cytosolic IκB-α/GAPDH | Proportion of Cytosolic Phosphorylated IκB-α | Nuclear p65/Oct1 |
---|---|---|---|
Vehicle | 0.92 ± 0.09, N = 7 | 0.55 ± 0.07, N = 4 | 0.26 ± 0.09, N = 7 |
1 uM BMS345541 | 0.74 ± 0.11, N = 7 | 0.68 ± 0.06, N = 4 | 0.46 ± 0.11, N = 7 |
Vehicle | 1.765 ± 0.47, N = 4 | 0.35 ± 0.9, N = 4 | 0.39 ± 0.05, N = 20 |
10 uM BMS345541 | 1.16 ± 0.20, N = 4 | 0.48 ± 0.08, N = 4 | 0.47 ± 0.08, N = 20 |
Vehicle | 1.39 ± 0.08, N = 12 | --------- | 1.20 ± 0.08, N = 6 |
50 uM BMS345541 | 1.1 ± 0.12, N = 13 | --------- | 1.12 ± 0.08, N = 7 |
Shown are the means ± SEM and N values for densitometric results obtained from the appropriate cell extracts of hemidiaphragm exposed to either vehicle or the indicated concentrations of BMS-345541. N represents the number of costal hemidiaphragms used to obtain the densitometric measurements from Western blots of the appropriate protein, using GAPDH as a loading control for cytosolic extracts and Oct 1 as a loading control for nuclear extracts. Separate vehicle controls were used for each concentration of BMS-345541 analyzed. BMS-345541 did not significantly influence cytosolic IκB-α expression, the proportion of phosphorylated IκB-α in the cytosol, or the nuclear expression of p65 at any concentration (1, 10, 50 μM).