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Flavonoid Fraction of Bergamot Juice Reduces LPS-Induced Inflammatory Response through SIRT1-Mediated NF-κB Inhibition in THP-1 Monocytes

机译:佛手柑汁的类黄酮成分通过SIRT1介导的THP-1单核细胞NF-κB抑制作用降低LPS诱导的炎症反应。

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摘要

Plant polyphenols exert anti-inflammatory activity through both anti-oxidant effects and modulation of pivotal pro-inflammatory genes. Recently, Citrus bergamia has been studied as a natural source of bioactive molecules with antioxidant activity, but few studies have focused on molecular mechanisms underlying their potential beneficial effects. Several findings have suggested that polyphenols could influence cellular function by acting as activators of SIRT1, a nuclear histone deacetylase, involved in the inhibition of NF-κB signaling. On the basis of these observations we studied the anti-inflammatory effects produced by the flavonoid fraction of the bergamot juice (BJe) in a model of LPS-stimulated THP-1 cell line, focusing on SIRT1-mediated NF-κB inhibition. We demonstrated that BJe inhibited both gene expression and secretion of LPS-induced pro-inflammatory cytokines (IL-6, IL-1β, TNF-α) by a mechanism involving the inhibition of NF-κB activation. In addition, we showed that BJe treatment reversed the LPS-enhanced acetylation of p65 in THP-1 cells. Interestingly, increasing concentrations of Sirtinol were able to suppress the inhibitory effect of BJe via p65 acetylation, underscoring that NF-κB–mediated inflammatory cytokine production may be directly linked to SIRT1 activity. These results suggest that BJe may be useful for the development of alternative pharmacological strategies aimed at reducing the inflammatory process.
机译:植物多酚通过抗氧化作用和关键的促炎基因的调节发挥抗炎活性。最近,对柑桔作为具有抗氧化活性的生物活性分子的天然来源进行了研究,但是很少有研究集中在潜在的潜在有益作用的分子机制上。一些发现表明,多酚可能通过充当SIRT1(一种核组蛋白脱乙酰基酶)的激活剂来影响细胞功能,SIRT1参与了NF-κB信号的抑制。基于这些观察结果,我们在LPS刺激的THP-1细胞系模型中研究了佛手柑汁(BJe)的类黄酮成分产生的抗炎作用,重点是SIRT1介导的NF-κB抑制作用。我们证明BJe通过涉及抑制NF-κB活化的机制抑制LPS诱导的促炎性细胞因子(IL-6,IL-1β,TNF-α)的基因表达和分泌。此外,我们显示BJe处理可逆转THP-1细胞中LPS增强的p65乙酰化作用。有趣的是,西地替诺浓度的增加能够通过p65乙酰化抑制BJe的抑制作用,强调NF-κB介导的炎性细胞因子的产生可能与SIRT1活性直接相关。这些结果表明,BJe可能有助于开发旨在减少炎症过程的替代药理策略。

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