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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >ErMiao San Inhibits Angiogenesis in Rheumatoid Arthritis by Suppressing JAK/STAT Signaling Pathways
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ErMiao San Inhibits Angiogenesis in Rheumatoid Arthritis by Suppressing JAK/STAT Signaling Pathways

机译:通过抑制JAK / STAT信号通路,Ermiao SAD抑制类风湿性关节炎中的血管生成

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摘要

ErMiao San (EMS) is composed of the Cortex Phellodendri chinensis and Atractylodes lancea, and it has the function of eliminating heat and excreting dampness in terms of traditional Chinese medicine to damp heat syndrome. Previous reports indicate that EMS possesses anti-inflammatory activity; however, its action on angiogenesis of rheumatoid arthritis (RA) has not been clarified. The present study aims to determine the antiangiogenic activity of EMS in collagen-induced arthritis (CIA) mice and in various angiogenesis models. Our data showed that EMS (5?g/kg) markedly reduced the immature blood vessels in synovial membrane tissues of inflamed joints from CIA mice. It also inhibited vascular endothelial growth factor (VEGF)-induced microvessel sprout formation ex vivo. Meanwhile, EMS suppressed VEGF-induced migration, invasion, adhesion, and tube formation of human umbilical vein endothelial cells (HUVECs). Moreover, EMS significantly reduced the expression of angiogenic activators including interleukin (IL)-1β, IL-6, and tumor necrosis factor-alpha (TNF-α) in synovium of CIA mice. More interestingly, EMS blocked the autophosphorylation of VEGF-induced JAK1, STAT1, and STAT6 in CIA mice and VEGF-induced HUVECs. These findings suggest for the first time that EMS possesses the antiangiogenic effect in RA in vivo, ex vivo, and in vitro by interrupting the targeting of JAK/STAT activation.
机译:Ermiao San(EMS)由Cortex Phellodendri Chinensis和Atractylodes Lankea组成,并且它具有在中药中消除热量和排泄湿度的功能,以潮湿的热综合征。之前的报告表明,EMS具有抗炎活动;然而,它对类风湿性关节炎(RA)的血管生成的作用尚未澄清。本研究旨在确定胶原蛋白诱导的关节炎(CIA)小鼠和各种血管生成模型中EMS的抗血管生成活性。我们的数据表明,EMS(5?G / kg)显着降低了CIA小鼠发炎关节的滑膜组织中的未成熟血管。它还抑制血管内皮生长因子(VEGF)诱导的微血管芽形成离体。同时,EMS抑制了人脐静脉内皮细胞(HUVECS)的VEGF诱导的迁移,侵袭,粘附和管形成。此外,EMS显着降低了CIA小鼠的中白素蛋白(IL)-1β,IL-6和肿瘤坏死因子-α(TNF-α)的血管生成激活剂的表达。更有趣的是,EMS阻断了CIA小鼠和VEGF诱导的HUVEC中VEGF诱导的JAK1,Stat1和Stat6的自磷酸化。这些研究结果表明EMS首次在体内,exVivo和体外具有抗血管生成作用,通过中断JAK / STAT激活的靶向。

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