Liu Chun-Ping, Liu Jian-Xing, Gu Jiangyong, Liu Fang, Li Jin-Hua, Wu Shou-Hai, Wu Qing-He, Li Long-Mei, Yang Hai-Long, Wang Lei, Li Xiong
The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Dongguan and Guangzhou University of Chinese Medicine Cooperative Academy of Mathematical Engineering for Chinese Medicine, Dongguan, China.
Front Pharmacol. 2021 Jan 11;11:580064. doi: 10.3389/fphar.2020.580064. eCollection 2020.
Caffeoylquinic acids, coumarins and dicaffeoyl derivatives are considered to be three kinds of the most abundant bioactive components in , an anti-inflammatory herb mainly found in Southern Asia. The combined anti-inflammatory effect of three typical constituents C + R + I (chlorogenic acid + rosmarinic acid + isofraxidin) from this plant has been investigated. The result implies that targeting the MAPK-NF-κB pathway would be one of the major mechanisms involved, using LPS stimulated RAW 264.7 cells as model and LPS-induced acute lung injury in mice as model. C + R + I can significantly suppress the levels of nitric oxide (NO), pro-inflammatory cytokines, and inhibit iNOS and COX-2 expression in LPS-treated RAW264.7 macrophage cells. Western blot analysis showed that C + R + I suppressed phosphorylation of NF-κB and MAPK, including phosphorylation of p65-NF-κB, IKB, ERK, JNK and P38. Besides, C + R + I suppressed MPO protein expression, but promoted SOD and HO-1 expression, and the related targets for C, R, and I were also predicted by molecular docking. This indicated that C + R + I could alleviate oxidative stress induced by LPS, which were further verified in the model of mice with acute lung injury through the measurement of corresponding inflammatory mediators and the analysis of immunehistochemistry.
咖啡酰奎宁酸、香豆素和二咖啡酰衍生物被认为是一种主要生长在南亚的抗炎草药中三种含量最为丰富的生物活性成分。已对该植物中三种典型成分C + R + I(绿原酸+迷迭香酸+异秦皮啶)的联合抗炎作用进行了研究。结果表明,以脂多糖刺激的RAW 264.7细胞为模型、以脂多糖诱导的小鼠急性肺损伤为模型,靶向丝裂原活化蛋白激酶-核因子κB(MAPK-NF-κB)信号通路可能是其中的主要机制之一。C + R + I可显著抑制脂多糖处理的RAW264.7巨噬细胞中一氧化氮(NO)、促炎细胞因子的水平,并抑制诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达。蛋白质免疫印迹分析表明,C + R + I可抑制NF-κB和MAPK的磷酸化,包括p65-NF-κB、IκB、细胞外调节蛋白激酶(ERK)、应激活化蛋白激酶(JNK)和p38的磷酸化。此外,C + R + I可抑制髓过氧化物酶(MPO)蛋白表达,但促进超氧化物歧化酶(SOD)和血红素加氧酶-1(HO-1)的表达,还通过分子对接预测了C、R和I的相关靶点。这表明C + R + I可减轻脂多糖诱导的氧化应激,通过测量相应的炎症介质和免疫组化分析在急性肺损伤小鼠模型中进一步验证了这一点。