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Received for publication September 7, 2004.
Revised November 4, 2004.
Accepted for publication November 9, 2004.
Glabridin, a flavonoid present in licorice extract, is
known to have antimicrobial, anti-inflammatory and
cardiovascular protective activities. In the present
study, we report the inhibitory effect of glabridin on
nitric oxide (NO) production and inducible nitric oxide
(iNOS) gene expression in murine macrophages. Glabridin
attenuated lipopolysaccharide (LPS)-induced NO
production in isolated mouse peritoneal macrophages and
RAW 264.7 cells, a mouse macrophage-like cell line.
Moreover, iNOS mRNA expression was also blocked by
glabridin treatment in LPS-stimulated RAW 264.7 cells.
Further study demonstrated that the LPS-induced NF-&
[kappa]B/Rel DNA binding activity and NF-
B/Rel-
dependent reporter gene activity were significantly
inhibited by glabridin in RAW 264.7 cells and that this
effect was mediated through the inhibition of inhibitory
factor-
B degradation and p65 nuclear
translocation. Moreover, reactive oxygen species
generation was also suppressed by glabridin treatment in
RAW 264.7 cells. In contrast, the activity of mitogen-
activated protein kinases was unaffected by glabridin
treatment. In animal model, in vivo administration of
glabridin increased the rate of survival of LPS-treated
mice and inhibited LPS-induced increase in plasma
concentrations of nitrite/nitrate and tumor necrosis
factor-
. Collectively, these data suggest that
glabridin inhibits NO production and iNOS gene
expression by blocking NF-
B/Rel activation and
that this effect was mediated, at least in part, by
inhibiting reactive oxygen species generation.
Furthermore, in vivo anti-inflammatory effect of
glabridin suggests a possible therapeutic application of
this agent in inflammatory diseases.
Key words:
NF-
B/Rel, glabridin, iNOS, licorice, nitric oxide, reactive oxygen species
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