Yuan Yun, Hu Qiongying, Liu Lu, Xie Fan, Yang Luyao, Li Yuchen, Zhang Chuantao, Chen Hongqing, Tang Jianyuan, Shen Xiaofei
Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
College of Medical Technology, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Front Pharmacol. 2022 Mar 7;13:817596. doi: 10.3389/fphar.2022.817596. eCollection 2022.
Dehydrocostus lactone (DCL) is a major sesquiterpene lactone isolated from , a traditional Chinese herbal medicine that used to treat gastrointestinal diseases. This study aimed to examine the therapeutic effects of DCL on dextran sulfate sodium (DSS)-induced colitis with a focus on identifying the molecular mechanisms involved in DCL-mediated anti-inflammatory activity in macrophages. First, oral administration of DCL (5-15 mg/kg) not only ameliorated symptoms of colitis and colonic barrier injury, but also inhibited the expression of proinflammatory cytokines and myeloperoxidase in colon tissues in DSS-challenged mice. Furthermore, DCL also exhibited significant anti-inflammatory activity in LPS/IFNγ-stimulated RAW264.7 macrophages. Importantly, DCL significantly suppressed the phosphorylation and degradation of IκBα and subsequent NF-κB nuclear translocation, and enhanced the nuclear accumulation of Nrf2 in LPS/IFNγ-treated RAW264.7 cells. Mechanistically, DCL could directly interact with IKKα/β and Keap1, thereby leading to the inhibition of NF-κB signalling and the activation of Nrf2 pathway. Furthermore, DCL-mediated actions were abolished by dithiothreitol, suggesting a thiol-mediated covalent linkage between DCL and IKKα/β or Keap1. These findings demonstrated that DCL ameliorates colitis by targeting NF-κB and Nrf2 signalling, suggesting that DCL may be a promising candidate in the clinical treatment of colitis.
脱氢木香内酯(DCL)是从一种用于治疗胃肠道疾病的传统中草药中分离出的一种主要倍半萜内酯。本研究旨在研究DCL对葡聚糖硫酸钠(DSS)诱导的结肠炎的治疗作用,重点是确定DCL介导的巨噬细胞抗炎活性所涉及的分子机制。首先,口服DCL(5-15mg/kg)不仅改善了结肠炎症状和结肠屏障损伤,还抑制了DSS攻击小鼠结肠组织中促炎细胞因子和髓过氧化物酶的表达。此外,DCL在LPS/IFNγ刺激的RAW264.7巨噬细胞中也表现出显著的抗炎活性。重要的是,DCL显著抑制IκBα的磷酸化和降解以及随后的NF-κB核转位,并增强LPS/IFNγ处理的RAW264.7细胞中Nrf2的核积累。机制上,DCL可直接与IKKα/β和Keap1相互作用,从而导致NF-κB信号传导的抑制和Nrf2途径的激活。此外,二硫苏糖醇消除了DCL介导的作用,表明DCL与IKKα/β或Keap1之间存在硫醇介导的共价连接。这些发现表明,DCL通过靶向NF-κB和Nrf2信号传导改善结肠炎,提示DCL可能是结肠炎临床治疗中有前景的候选药物。