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Effects of daphnetin on the autophagy signaling pathway of fibroblast-like synoviocytes in rats with collagen-induced arthritis (CIA) induced by TNF-alpha

机译:TNF-α诱导的胶原诱导的关节炎大鼠成纤维细胞样Synociytes自噬信号通路的影响

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摘要

Daphnetin (DAP), an active ingredient extracted from Daphne odora, has pharmacological effects such as anti-inflammatory, antioxidation and anti-tumor properties. The current study aims to investigate the relationship between the anti-rheumatoid effect of DAP and the inhibition of both the PI3K/AKT/inTOR and autophagy signaling pathways. DAP inhibited the proliferation of CIA-FLS in a dose-dependent manner and induce apoptosis, accelerated the G1/G0 phase and inhibited the S phase. DAP reduced the phosphorylation of AKT and mTOR and the expression of Atg5, Beclin-1 and LC3-II/LC3-1 in CIA-FLS induced by TNF-alpha. DAP also reduced the inflammatory response in CIA-FLS induced by TNF-alpha by inhibiting the cytokine expression of TNF-alpha, IL-6, TGF-beta, IL-17, and INF-gamma and promoting IL-10 expression. Overall, DAP inhibited the proliferation of CIA-FLS by down-regulating the PI3K/AKT/mTOR signaling pathway and inhibited autophagy in order to induces apoptosis, which may be potential therapeutic approach in treatment of RA.
机译:从Daphne Odora提取的活性成分,具有药理学效应,如抗炎,抗氧化和抗肿瘤性质。目前的研究旨在探讨DAP的抗类风湿效应与PI3K / AKT / INTOR和自噬信号通路的抑制作用。 DAP以剂量依赖性方式抑制CIA-FL的增殖,诱导细胞凋亡,加速G1 / G0相并抑制S期。 DAP降低了AKT和MTOR的磷酸化和TNF-α诱导的CIA-FL中的ATG5,BECLIN-1和LC3-II / LC3-1的表达。通过抑制TNF-α,IL-6,TGF-Beta,IL-17和INF-γ的细胞因子表达,DAP还降低了TNF-α诱导的CIA-FL的炎症反应。总的来说,DAP通过向下调节PI3K / AKT / MTOR信号传导途径并抑制自噬抑制CIA-FL的增殖,以诱导细胞凋亡,这可能是治疗RA的潜在治疗方法。

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