The novel flavonoid compound 3'-hydroxyfarrerol (IdB 1031) was tested
in a number of in vitro experiments in order to ascertain its effects
on some functions and products of human phagocytes. We found that IdB
1031 did not depress neutrophil phagocytosis and chemotaxis, whereas a
t a concentration of 10(-4) M it significantly (p < 0.05) reduced the
fMLP-triggered neutrophil production of superoxide anion. At the same
concentration, the compound decreased the release of neutrophil elasta
se and myeloperoxidase from neutrophils (p < 0.05). We also found evid
ence that IdB 1031 is a non competitive, reversible inhibitor of human
neutrophil elastase (K-i 200 mu m) Finally, IdB 1031 at the concentra
tion of 10(-5) M significantly reduced the release of tumor necrosis f
actor-alpha and interleukin-8 from monocytes (p < 0.05). We conclude t
hat in spite of the moderate activity displayed by IdB 1031, these fin
dings add to our current knowledge on the spectrum of the antiinflamma
tory activities of flavonoids.