a Key Laboratory for Space Bioscience and Space Biotechnology, School of Life Sciences , Northwestern Polytechnical University , Xi'an , Shaanxi , P. R. China.
b Desert Plants & Ecological Civilization Research Center , Northwest University , Xi'an , Shaanxi , P. R. China.
Pharm Biol. 2017 Dec;55(1):799-809. doi: 10.1080/13880209.2017.1280514.
Sonchus oleraceus L. (Asteraceae) (SO) is a dietary and traditional medicinal plant in China. However, its underlying mechanism of action as an anti-inflammatory agent is not known.
This study evaluates the anti-inflammatory activity of aqueous extract of SO.
The extract of SO was used to treat RAW 264.7 cells (in the working concentrations of 500, 250, 125, 62.5, 31.3 and 15.6 μg/mL) for 24 h. Pro-inflammatory cytokines and mediators produced in LPS-stimulated RAW 264.7 cells were assessed. Meanwhile, the expression level of TLR-4, COX-2, pSTATs and NF-κB was tested. Moreover, the anti-inflammatory activity of the extract in vivo was assessed using xylene-induced mouse ear oedema model and the anti-inflammatory compounds in the extracts were analyzed by HPLC-MS.
SO extract significantly inhibited the production of pro-inflammatory cytokines and mediators at gene and protein levels with the concentration of 31.3 μg/mL, and suppressed the expression of TLR-4, COX-2, NF-κB and pSTAT in RAW 264.7 cells. The anti-inflammatory activity of SO in vivo has significant anti-inflammatory effects with the concentration of 250 and 125 mg/kg, and less side effect on the weights of the mice at the concentration of 250 mg/kg. Moreover, HPLC-MS analysis revealed that the anti-inflammatory compounds in the extract were identified as villosol, ferulaic acid, β-sitosterol, ursolic acid and rutin.
This study indicated that SO extract has anti-inflammatory effects in vitro and in vivo, which will be further developed as novel pharmacological strategies in order to defeat inflammatory diseases.
菊科植物苦苣菜(SO)在中国既是一种食用植物,也是一种传统药用植物。然而,其作为抗炎剂的作用机制尚不清楚。
本研究评估了 SO 水提物的抗炎活性。
使用 SO 提取物(工作浓度分别为 500、250、125、62.5、31.3 和 15.6μg/mL)处理 RAW 264.7 细胞 24h,评估 LPS 刺激的 RAW 264.7 细胞中产生的促炎细胞因子和介质。同时,检测 TLR-4、COX-2、pSTAT 和 NF-κB 的表达水平。此外,采用二甲苯诱导的小鼠耳肿胀模型评估提取物的体内抗炎活性,并通过 HPLC-MS 分析提取物中的抗炎化合物。
SO 提取物在 31.3μg/mL 浓度下显著抑制促炎细胞因子和介质的基因和蛋白水平表达,并抑制 RAW 264.7 细胞中 TLR-4、COX-2、NF-κB 和 pSTAT 的表达。SO 在体内的抗炎活性在 250 和 125mg/kg 浓度下具有显著的抗炎作用,在 250mg/kg 浓度下对小鼠体重的副作用较小。此外,HPLC-MS 分析表明,提取物中的抗炎化合物被鉴定为维索醇、阿魏酸、β-谷甾醇、熊果酸和芦丁。
本研究表明,SO 提取物具有体外和体内抗炎作用,可进一步开发为新型药理策略,以对抗炎症性疾病。