Chen Lin-Lin, Zhang Hao-Jun, Chao Jung, Liu Jun-Feng
Key Laboratory of Traditional Chinese Medicine Resource and Compound Prescription, Ministry of Education, Hubei University of Chinese Medicine, Wuhan 430065, PR China.
Department of Pharmacology, China-Japan Friendship Hospital, Beijing 100029, China.
J Ethnopharmacol. 2017 May 23;204:107-117. doi: 10.1016/j.jep.2017.04.017. Epub 2017 Apr 21.
Artemisia argyi is a herbal medicine traditionally used in Asia for the treatment of bronchitis, dermatitis and arthritis. Recent studies revealed the anti-inflammatory effect of essential oil in this plant. However, the mechanisms underlying the therapeutic potential have not been well elucidated. The present study is aimed to verify its anti-inflammatory effect and investigate the probable mechanisms.
The essential oil from Artemisia argyi (AAEO) was initially tested against LPS-induced production of inflammatory mediators and cytokines in RAW264.7 macrophages. Protein and mRNA expressions of iNOS and COX-2 were determined by Western blotting and RT-PCR analysis, respectively. The effects on the activation of MAPK/NF-κB/AP-1 and JAK/STATs pathway were also investigated by western blot. Meanwhile, in vivo anti-inflammatory effect was examined by histologic and immunohistochemical analysis in TPA-induced mouse ear edema model.
The results of in vitro experiments showed that AAEO dose-dependently suppressed the release of pro-inflammatory mediators (NO, PGE and ROS) and cytokines (TNF-α, IL-6, IFN-β and MCP-1) in LPS-induced RAW264.7 macrophages. It down-regulated iNOS and COX-2 protein and mRNA expression but did not affect the activity of these two enzymes. AAEO significantly inhibited the phosphorylation of JAK2 and STAT1/3, but not the activation of MAPK and NF-κB cascades. In animal model, oral administration of AAEO significantly attenuated TPA-induced mouse ear edema and decreased the protein level of COX-2.
AAEO suppresses inflammatory responses via down-regulation of the JAK/STATs signaling and ROS scavenging, which could contribute, at least in part, to the anti-inflammatory effect of AAEO.
艾叶是一种传统上在亚洲用于治疗支气管炎、皮炎和关节炎的草药。最近的研究揭示了该植物中精油的抗炎作用。然而,其治疗潜力背后的机制尚未得到充分阐明。本研究旨在验证其抗炎作用并探究可能的机制。
首先测试了艾叶精油(AAEO)对脂多糖(LPS)诱导的RAW264.7巨噬细胞中炎症介质和细胞因子产生的影响。分别通过蛋白质印迹法和逆转录-聚合酶链反应(RT-PCR)分析测定诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的蛋白质和mRNA表达。还通过蛋白质印迹法研究了其对丝裂原活化蛋白激酶(MAPK)/核因子κB(NF-κB)/活化蛋白-1(AP-1)和Janus激酶(JAK)/信号转导子和转录激活子(STATs)信号通路激活的影响。同时,在佛波酯(TPA)诱导的小鼠耳肿胀模型中,通过组织学和免疫组织化学分析检测了其体内抗炎作用。
体外实验结果表明,AAEO在脂多糖诱导的RAW264.7巨噬细胞中呈剂量依赖性地抑制促炎介质(一氧化氮、前列腺素E和活性氧)和细胞因子(肿瘤坏死因子-α、白细胞介素-6、干扰素-β和单核细胞趋化蛋白-1)的释放。它下调了iNOS和COX-2的蛋白质和mRNA表达,但不影响这两种酶的活性。AAEO显著抑制JAK2和STAT1/3的磷酸化,但不影响MAPK和NF-κB信号级联的激活。在动物模型中,口服AAEO显著减轻了TPA诱导的小鼠耳肿胀,并降低了COX-2的蛋白质水平。
AAEO通过下调JAK/STATs信号通路和清除活性氧来抑制炎症反应,这至少部分有助于AAEO的抗炎作用。