Effects of HO-1 products, bilirubin, CO, and Fe2+ on IFN-γ-induced
iNOS expression/NO release. Primary microglia were treated with 20 ng/ml IFN-γ
for 12 h (A) or 72 h (B)
in the absence or presence of the indicated amount of BR, CORM, and
FeSO4. iNOS protein expression was measured by Western blotting
(A) and the amount of nitrite converted from NO in
the media was measured using the Griess reagents (B).
Values in B are mean ± SEM of three samples.
*p < 0.05 compared with IFN-γ. The data are
representative of three independent experiments.