首页> 外文期刊>The British Journal of Nutrition >Cocoa polyphenols suppress TNF- alpha-induced vascular endothelial growth factor expression by inhibiting phosphoinositide 3-kinase (PI3K) and mitogen-activated protein kinase kinase-1 (MEK1) activities in mouse epidermal cells.
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Cocoa polyphenols suppress TNF- alpha-induced vascular endothelial growth factor expression by inhibiting phosphoinositide 3-kinase (PI3K) and mitogen-activated protein kinase kinase-1 (MEK1) activities in mouse epidermal cells.

机译:可可多酚通过抑制小鼠表皮细胞中的磷酸肌醇3激酶(PI3K)和有丝分裂原激活的蛋白激酶激酶1(MEK1)活性来抑制TNF-α诱导的血管内皮生长因子的表达。

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摘要

Cocoa polyphenols have antioxidant and anti-inflammatory effects. TNF- alpha is a pro-inflammatory cytokine that has a vital role in the pathogenesis of inflammatory diseases such as cancer and psoriasis. Vascular endothelial growth factor (VEGF) expression is associated with tumorigenesis, CVD, rheumatoid arthritis and psoriasis. We tested whether cocoa polyphenol extract (CPE) inhibited TNF- alpha-induced VEGF expression in promotion-sensitive JB6 mouse epidermal cells. CPE significantly inhibited TNF- alpha-induced up-regulation of VEGF via reducing TNF- alpha-induced activation of the nuclear transcription factors activator protein-1 (AP-1) and NF- kappaB, which are key regulators of VEGF expression. CPE also inhibited TNF- alpha-induced phosphorylation of protein kinase B (Akt) and extracellular signal-regulated kinase. CPE blocked activation of their downstream kinases, p70 kDa ribosomal protein S6 kinase and p90 kDa ribosomal protein S6 kinase. CPE suppressed phosphoinositide 3-kinase (PI3K) activity via binding PI3K directly. CPE did not affect TNF- alpha-induced phosphorylation of mitogen-activated protein kinase kinase-1 (MEK1) but suppressed TNF- alpha-induced MEK1 activity. Collectively, these results indicate that CPE reduced TNF- alpha-induced up-regulation of VEGF by directly inhibiting PI3K and MEK1 activities, which may contribute to its chemopreventive potential.
机译:可可多酚具有抗氧化和抗炎作用。 TNF-α是促炎细胞因子,在诸如癌症和牛皮癣的炎性疾病的发病机理中具有至关重要的作用。血管内皮生长因子(VEGF)的表达与肿瘤发生,CVD,类风湿性关节炎和牛皮癣相关。我们测试了可可多酚提取物(CPE)是否在促进敏感性JB6小鼠表皮细胞中抑制TNF-α诱导的VEGF表达。 CPE通过减少TNF-α诱导的核转录因子激活蛋白1(AP-1)和NF-κB的激活而显着抑制TNF-α诱导的VEGF上调,这是VEGF表达的关键调节因子。 CPE还抑制TNF-α诱导的蛋白激酶B(Akt)和细胞外信号调节激酶的磷酸化。 CPE阻断了其下游激酶,p70 kDa核糖体蛋白S6激酶和p90 kDa核糖体蛋白S6激酶的激活。 CPE通过直接结合PI3K抑制了磷酸肌醇3-激酶(PI3K)的活性。 CPE不会影响TNF-α诱导的丝裂原激活的蛋白激酶激酶1(MEK1)的磷酸化,但会抑制TNF-α诱导的MEK1活性。总而言之,这些结果表明,CPE通过直接抑制PI3K和MEK1活性来降低TNF-α诱导的VEGF上调,这可能有助于其化学预防潜力。

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