Centro de Estudos Farmacêuticos-Faculdade de Farmácia, Universidade de Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.
J Ethnopharmacol. 2011 Jan 27;133(2):818-27. doi: 10.1016/j.jep.2010.11.018. Epub 2010 Nov 12.
Aqueous extracts of Cymbopogon citratus (Cy) leaves are used in traditional medicine for the treatment of inflammatory conditions, however, little is known about their mechanism of action.
The aim of this study is to explore the anti-inflammatory properties of Cymbopogon citratus leaves and their polyphenol-rich fractions (PFs), as well its mechanism of action in murine macrophages.
A lipid- and essential oil-free infusion of Cy leaves was prepared (Cy extract) and fractionated by column chromatography. Anti-inflammatory properties of Cy extract (1.115 mg/ml) and its PFs, namely phenolic acids (530 μg/ml), flavonoids (97.5 μg/ml) and tannins (78 μg/ml), were investigated using lipopolysaccharide (LPS)-stimulated Raw 264.7 macrophages as in vitro model. As inflammatory parameters, nitric oxide (NO) production was evaluated by Griess reaction, as well as effects on cyclooxygenase-2 (COX-2), inducible NO synthase (iNOS) expression and on intracellular signaling pathways activation, which were analyzed by Western blot using specific antibodies.
Cy extract inhibited iNOS expression, NO production and various LPS-induced pathways like p38 mitogen-activated protein kinase (MAPK), c-jun NH(2)-terminal kinase (JNK) 1/2 and the transcription nuclear factor (NF)-κB. The extracellular signal-regulated kinase (ERK) 1/2 and the phosphatidylinositol-3-kinase (PI3K)/Akt activation were not affected by Cy extract. Both phenolic acid- and tannin-rich fractions significantly inhibited NF-κB activation, iNOS expression and NO production but none of the PFs modulated MAPKs or PI3K/Akt activation. Neither Cy extract nor PFs affected LPS-induced COX-2 expression but LPS-induced PGE(2) production is inhibited by Cy extract and by phenolic acid-rich fraction.
Our data provide evidence that support the usage of Cymbopogon citratus leaves extract in traditional medicine, and suggest that Cy, in particular its polyphenolic compounds, could constitute a natural source of a new and safe anti-inflammatory drug.
香茅(Cy)叶的水提物在传统医学中用于治疗炎症性疾病,但对其作用机制知之甚少。
本研究旨在探讨香茅叶及其多酚丰富部分(PFs)的抗炎特性,以及其在鼠巨噬细胞中的作用机制。
制备香茅叶的无脂和精油浸膏(Cy 浸膏)并通过柱色谱法进行分离。使用脂多糖(LPS)刺激的 Raw 264.7 巨噬细胞作为体外模型,研究 Cy 浸膏(1.115mg/ml)及其 PFs(即酚酸(530μg/ml)、类黄酮(97.5μg/ml)和单宁(78μg/ml))的抗炎特性。通过格里斯反应评估一氧化氮(NO)的产生作为炎症参数,以及对环氧化酶-2(COX-2)、诱导型一氧化氮合酶(iNOS)表达和细胞内信号通路激活的影响,通过使用特异性抗体的 Western blot 进行分析。
Cy 浸膏抑制 iNOS 表达、NO 产生和各种 LPS 诱导的途径,如丝裂原活化蛋白激酶(MAPK)p38、c-jun NH2-末端激酶(JNK)1/2 和转录核因子(NF)-κB。细胞外信号调节激酶(ERK)1/2 和磷酸肌醇-3-激酶(PI3K)/Akt 激活不受 Cy 浸膏影响。酚酸和单宁丰富的部分均显著抑制 NF-κB 激活、iNOS 表达和 NO 产生,但 PFs 均不调节 MAPKs 或 PI3K/Akt 激活。Cy 浸膏和 PFs 均不影响 LPS 诱导的 COX-2 表达,但 Cy 浸膏和酚酸丰富的部分抑制 LPS 诱导的 PGE2 产生。
我们的数据提供了支持香茅叶提取物在传统医学中使用的证据,并表明 Cy,特别是其多酚化合物,可能构成一种新型安全抗炎药物的天然来源。