Aneja Rajesh, Odoms Kelli, Denenberg Alvin G, Wong Hector R
Division of Critical Care Medicine, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, and Children's Hospital Research Foundation, Cincinnati, OH, USA.
Crit Care Med. 2004 Oct;32(10):2097-103. doi: 10.1097/01.ccm.0000142661.73633.15.
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-alpha-mediated expression of the interleukin-8 gene in A549 cells.
Prospective laboratory study.
University laboratory.
A549 cells.
A549 cells were exposed to varying concentrations of theaflavin and analyzed for tumor necrosis factor-alpha-mediated interleukin-8 gene expression.
Theaflavin inhibited tumor necrosis factor-alpha-mediated interleukin-8 gene expression, as measured by luciferase assay and Northern blot analysis, at concentrations of 10 and 30 microg/mL. This effect appears to primarily involve inhibition of interleukin-8 transcription because theaflavin inhibited tumor necrosis factor-alpha-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-alpha-mediated activation of IkappaB kinase and subsequent activation of the IkappaB-alpha/nuclear factor-kappaB pathway. Theaflavin also significantly reduced tumor necrosis factor-alpha-mediated DNA binding of activator protein-1.
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 IkappaB kinase activation and activator protein-1 pathway.
茶已存在数百年,其药用特性在文献中已有记载,但从未得到充分证实。白细胞介素-8是人体内主要的中性粒细胞趋化因子和激活剂。我们测定了红茶衍生多酚茶黄素对肿瘤坏死因子-α介导的A549细胞中白细胞介素-8基因表达的影响。
前瞻性实验室研究。
大学实验室。
A549细胞。
将A549细胞暴露于不同浓度的茶黄素中,并分析肿瘤坏死因子-α介导的白细胞介素-8基因表达。
通过荧光素酶测定和Northern印迹分析,在浓度为10和30μg/mL时,茶黄素抑制了肿瘤坏死因子-α介导的白细胞介素-8基因表达。这种作用似乎主要涉及抑制白细胞介素-8转录,因为茶黄素抑制了用白细胞介素-8启动子-荧光素酶报告质粒瞬时转染的细胞中肿瘤坏死因子-α介导的白细胞介素-8启动子激活。此外,茶黄素抑制了肿瘤坏死因子-α介导的IκB激酶激活以及随后的IκB-α/核因子-κB途径激活。茶黄素还显著降低了肿瘤坏死因子-α介导的激活蛋白-1的DNA结合。
我们得出结论,茶黄素在体外是白细胞介素-8基因表达的有效抑制剂。这种作用的近端机制部分涉及抑制IκB激酶激活和激活蛋白-1途径。