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 |
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Format: | Artikel |
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. |
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ISSN: | 0090-3493 1530-0293 |
DOI: | 10.1097/01.CCM.0000142661.73633.15 |