Theaflavin, a black tea extract, is a novel anti-inflammatory compound

OBJECTIVE:Tea has been around for centuries, and its medicinal properties have been purported in the literature but never fully confirmed. Interleukin-8 is a principle neutrophil chemoattractant and activator in humans. We determined the effects of theaflavin, a black tea-derived polyphenol, on tumo...

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Veröffentlicht in:Critical care medicine 2004-10, Vol.32 (10), p.2097-2103
Hauptverfasser: Aneja, Rajesh, Odoms, Kelli, Denenberg, Alvin G, Wong, Hector R
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Sprache:eng
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Zusammenfassung:OBJECTIVE:Tea has been around for centuries, and its medicinal properties have been purported in the literature but never fully confirmed. Interleukin-8 is a principle neutrophil chemoattractant and activator in humans. We determined the effects of theaflavin, a black tea-derived polyphenol, on tumor necrosis factor-α-mediated expression of the interleukin-8 gene in A549 cells. DESIGN:Prospective laboratory study. SETTING:University laboratory. SUBJECTS:A549 cells. INTERVENTIONS:A549 cells were exposed to varying concentrations of theaflavin and analyzed for tumor necrosis factor-α-mediated interleukin-8 gene expression. MEASUREMENTS AND MAIN RESULTS:Theaflavin inhibited tumor necrosis factor-α-mediated interleukin-8 gene expression, as measured by luciferase assay and Northern blot analysis, at concentrations of 10 and 30 μg/mL. This effect appears to primarily involve inhibition of interleukin-8 transcription because theaflavin inhibited tumor necrosis factor-α-mediated activation of the interleukin-8 promoter in cells transiently transfected with an interleukin-8 promoter-luciferase reporter plasmid. In addition, theaflavin inhibited tumor necrosis factor-α-mediated activation of IκB kinase and subsequent activation of the IκB-α/nuclear factor-κB pathway. Theaflavin also significantly reduced tumor necrosis factor-α-mediated DNA binding of activator protein-1. CONCLUSIONS:We conclude that theaflavin is a potent inhibitor of interleukin-8 gene expression in vitro. The proximal mechanism of this effect involves, in part, inhibition of IκB kinase activation and activator protein-1 pathway.
ISSN:0090-3493
1530-0293
DOI:10.1097/01.CCM.0000142661.73633.15