首页> 美国卫生研究院文献>Oxidative Medicine and Cellular Longevity >Yiqi-Huoxue Granule (YQHX) Downregulates Prothrombotic Factors by Modulating KLF2 and NF-κB in HUVECs following LPS Stimulation
【2h】

Yiqi-Huoxue Granule (YQHX) Downregulates Prothrombotic Factors by Modulating KLF2 and NF-κB in HUVECs following LPS Stimulation

机译:益气活血颗粒(YQHX)通过刺激LPS刺激HUVECs中的KLF2和NF-κB下调血栓形成因子。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The Yiqi-Huoxue granule (YQHX) is a traditional Chinese medication widely used in the therapy of the traditional Chinese medicine diagnosis “Qi deficiency” or “blood stasis” in China. Both these symptoms are related to inflammation, but the mechanisms of YQHX against inflammation are largely unknown. Thus, our present study investigated the effects of YQHX on regulating inflammatory responses induced by lipopolysaccharides (LPS) in HUVECs. Our data found that YQHX remarkably inhibits the production of prothrombotic factors, plasminogen activator inhibitor-1 (PAI-1) and tissue factor (TF), while it upregulates the protein expression of Kruppel-like factor 2 (KLF2). The increase in PAI-1 and TF was significantly attenuated through a transgenic knockdown in KLF2 with a Lenti-shKLF2 vector. YQHX also decreases the phosphorylation of nuclear factor-κB (NF-κB) p65 and IκB following LPS stimulation, and it effectively suppresses PAI-1 and TF via a NF-κB-dependent mechanism. Taken together, our results suggest that YQHX provides a notable antithrombotic activity via regulating the KLF2 expression and NF-κB signaling pathway in HUVECs. The KLF2 and NF-κB may be potential therapeutic targets for interventions of inflammation associated with atherosclerosis.
机译:益气活血颗粒(YQHX)是一种中药,在中国诊断为“气虚”或“血瘀”的中药中被广泛使用。这两种症状都与炎症有关,但是YQHX抵抗炎症的机制尚不清楚。因此,我们目前的研究调查了YQHX对调节HUVEC中脂多糖(LPS)诱导的炎症反应的影响。我们的数据发现,YQHX显着抑制血栓前因子,纤溶酶原激活物抑制剂1(PAI-1)和组织因子(TF)的产生,同时上调Kruppel样因子2(KLF2)的蛋白表达。通过使用Lenti-shKLF2载体在KLF2中进行转基因敲低可以显着减弱PAI-1和TF的增加。 YQHX还可降低LPS刺激后核因子-κB(NF-κB)p65和IκB的磷酸化,并通过NF-κB依赖性机制有效抑制PAI-1和TF。两者合计,我们的结果表明YQHX通过调节HUVEC中的KLF2表达和NF-κB信号传导途径提供了显着的抗血栓形成活性。 KLF2和NF-κB可能是干预动脉粥样硬化相关炎症的潜在治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号