Zhang Yi, Chi-Yan Cheng Brian, Xie Ran, Xu Bing, Gao Xiao Yan, Luo Gan
School of Chinese Materia Medica, Beijing University of Chinese Medicine Beijing 100102 China
College of Professional and Continuing Education, Hong Kong Polytechnic University Hong Kong 999077 China.
RSC Adv. 2019 Mar 18;9(16):8912-8925. doi: 10.1039/c9ra00060g. eCollection 2019 Mar 15.
: inhalation solution (RIS) is a novel preparation derived from the injection, which has been clinically used to treat respiratory diseases such as pneumonia for more than twenty years in China. However, scant reports have been issued on its anti-inflammatory mechanisms. : we investigated the suppressive effect of RIS on inflammatory mediators and explored the underlying mechanism of action. : RIS freeze dried powder was characterized by HPLC analysis. Lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophage was selected as the cell model. The cell viability was determined by using the MTT assay. Moreover, the production of nitric oxide (NO) was measured by the Griess reaction. The protein secretions from inflammatory mediators were determined by the enzyme-linked immunosorbent assay (ELISA). The protein levels and enzyme activities were examined by Western blotting. The nuclear translocation of nuclear factor-kappa B (NF-κB), AP-1, and IRF3 was further explored by immunofluorescence assay. : the viability of the RAW 264.7 cells was not significantly changed after 24 h incubation with RIS concentration up to 400 μg mL. The RIS remarkably reduced the production of NO and prostaglandin E (PGE), and downregulated the expression of iNOS and COX-2. The concentrations of cytokines (IL-1β, IL-6, and TNF-α) and chemokines (MCP-1, CCL-5, and MIP-1α) in the culture medium were significantly decreased by the RIS treatment. Furthermore, the phosphorylation of IκB-α, IKKα/β, TBK1, ERK, p38, JNK, NF-κB, AP-1, and IRF3 was downregulated by the RIS treatment. The nuclear translocation of NF-κB, AP-1, and IRF3 was also inhibited after the RIS treatment. : the suppressive effect of RIS is associated with the regulated NF-κB, AP-1, and IRF3 and their upstream proteins. This study provides a pharmacological basis for the application of RIS in the treatment of inflammatory disorders.
吸入溶液(RIS)是一种从注射剂衍生而来的新型制剂,在中国已临床用于治疗肺炎等呼吸道疾病二十多年。然而,关于其抗炎机制的报道却很少。我们研究了RIS对炎症介质的抑制作用,并探讨了其潜在的作用机制。通过高效液相色谱(HPLC)分析对RIS冻干粉进行了表征。选择脂多糖(LPS)刺激的RAW 264.7巨噬细胞作为细胞模型。使用MTT法测定细胞活力。此外,通过格里斯反应测定一氧化氮(NO)的产生。通过酶联免疫吸附测定(ELISA)测定炎症介质的蛋白质分泌。通过蛋白质印迹法检测蛋白质水平和酶活性。通过免疫荧光测定进一步探索核因子-κB(NF-κB)、活化蛋白-1(AP-1)和干扰素调节因子3(IRF3)的核转位。在与浓度高达400μg/mL的RIS孵育24小时后,RAW 264.7细胞的活力没有显著变化。RIS显著降低了NO和前列腺素E(PGE)的产生,并下调了诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达。RIS处理显著降低了培养基中细胞因子(白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α)和趋化因子(单核细胞趋化蛋白-1、CC趋化因子配体5和巨噬细胞炎性蛋白-1α)的浓度。此外,RIS处理下调了IκB-α、IKKα/β、TBK1、细胞外信号调节激酶(ERK)、p38、应激活化蛋白激酶(JNK)、NF-κB、AP-1和IRF3的磷酸化。RIS处理后,NF-κB、AP-1和IRF3的核转位也受到抑制。RIS的抑制作用与NF-κB、AP-1和IRF3及其上游蛋白的调节有关。本研究为RIS在炎症性疾病治疗中的应用提供了药理学依据。