PT  - JOURNAL ARTICLE
AU  - Yu-Li Lin
AU  - Jen-Kun Lin
TI  - (−)-Epigallocatechin-3-gallate Blocks the Induction of Nitric Oxide Synthase by Down-Regulating Lipopolysaccharide-Induced Activity of Transcription Factor Nuclear Factor-κB
AID  - 10.1124/mol.52.3.465
DP  - 1997 Sep 01
TA  - Molecular Pharmacology
PG  - 465--472
VI  - 52
IP  - 3
4099  - http://molpharm.aspetjournals.org/content/52/3/465.short
4100  - http://molpharm.aspetjournals.org/content/52/3/465.full
SO  - Mol Pharmacol1997 Sep 01; 52
AB  - Nitric oxide (NO) plays an important role in inflammation and multiple stages of carcinogenesis. We investigated the effect of various tea polyphenols and caffeine on the induction of NO synthase (NOS) in thioglycollate-elicited and lipopolysaccharide (LPS)-activated peritoneal macrophages. Gallic acid (GA), (−)-epigallocatechin (EGC), and (−)-epigallocatechin-3-gallate (EGCG), the major tea catechin, were found to inhibit inducible NOS (iNOS) protein in activated macrophages. EGCG, a potent antitumor agent with anti-inflammatory and antioxidant properties, inhibited NO generation, as measured by the amount of nitrite released into the culture medium. Inhibition of NO production was observed when cells were cotreated with EGCG and LPS. iNOS activity in soluble extracts of lipopolysaccharide-activated macrophages treated with EGCG (5 and 10 μm) for 6–24 hr was significantly lower than that in macrophages without EGCG treatment. Western blot, reverse transcription-polymerase chain reaction, and Northern blot analyses demonstrated that significantly reduced 130-kDa protein and 4.5-kb mRNA levels of iNOS were expressed in lipopolysaccharide-activated macrophages with EGCG compared with those without EGCG. Electrophoretic mobility shift assay indicated that EGCG blocked the activation of nuclear factor-κB, a transcription factor necessary for iNOS induction. EGCG also blocked disappearance of inhibitor κB from cytosolic fraction. These results suggest that EGCG decreases the activity and protein levels of iNOS by reducing the expression of iNOS mRNA and the reduction could occur through prevention of the binding of nuclear factor-κB to the iNOS promoter, thereby inhibiting the induction of iNOS transcription.