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升麻素苷减轻脂多糖诱导的RAW 264.7巨噬细胞炎症反应。

Prim-O-glucosylcimifugin Attenuates Lipopolysaccharideinduced Inflammatory Response in RAW 264.7 Macrophages.

作者信息

Zhou Jie, Sun Yuan-Yuan, Sun Meng-Yao, Mao Wei-An, Wang Li, Zhang Jian, Zhang Hong

机构信息

Department of Dermatology, Seventh People's Hospital of Shanghai University of TCM, Shanghai 200137, China.

Department of Clinical Medicine, Bengbu Medical College, Anhui 233000, China.

出版信息

Pharmacogn Mag. 2017 Jul-Sep;13(51):378-384. doi: 10.4103/pm.pm_323_16. Epub 2017 Jul 19.

Abstract

BACKGROUND

Radix Saposhnikoviae (RS) exerts anti-inflammatory, analgesic, antipyretic, antioxidation effects and has been used in traditional Chinese medicine to treat common colds, headache, and rheumatoid arthritis. Prim-O-glucosylcimifugin (POG) is the highest content chromone and one of the major active constituents in RS.

OBJECTIVE

The study was aimed to explore the anti-inflammation effects of POG in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages.

MATERIALS AND METHODS

Cell viability was detected by Cell Counting Kit-8 assay. Production of nitric oxide (NO), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and IL-6 was assessed by enzyme-linked immunosorbent assay. Real-time polymerase chain reaction and Western blot were performed to analyze mRNA and protein levels, respectively.

RESULTS

During the whole experiment, 15, 50, and 100 μg/mL of POG had no cytotoxicity on RAW 264.7 cells. POG dose-dependently inhibited the production of NO, TNF-α, IL-1β, and IL-6 that were induced by LPS. POG treatment downregulated the mRNA and protein expression inducible NO synthase (iNOS) and cyclooxygenase 2 (COX-2) in LPS-activated RAW 264.7 macrophages in a concentration-dependent manner. Furthermore, LPS-induced JAK2/STAT3 activation was prevented in RAW 264.7 macrophages by POG treatment. STAT3 overexpression significantly reversed the effects of POG on LPS-activated RAW 264.7 macrophages.

CONCLUSION

These results demonstrate that POG exerts anti-inflammatory effects through the inhibition of iNOS and COX-2 expression by inhibiting the phosphorylation of JAK2/STAT3.

SUMMARY

POG exerts anti-inflammatory effects in RAW 264.7 macrophages through the inhibition of iNOS and COX-2 expression by inhibiting JAK2/STAT3 signaling. LPS: Lipopolyssacharide; NO: Nitric oxide; TNF-α: Tumor necrosis factor-α; IL: Interleukin; RS: Radix Saposhnikoviae; POG: Prim-O-glucosylcimifugin; iNOS: Inducible NO synthase; COX2: Cyclooxygenase; FBS: Fetal bovine serum; DMSO: Dimethylsulfoxide; CCK-8: Cell Counting Kit; RIPA: Radio immunoprecipitation assay buffer; ECL: Enhanced chemiluminescence; SD: Standard deviation; ELISA: Enzyme-Linked immunosorbent assay.

摘要

背景

防风具有抗炎、镇痛、解热、抗氧化作用,在传统中药中用于治疗感冒、头痛和类风湿性关节炎。升麻素苷是防风中含量最高的色原酮和主要活性成分之一。

目的

本研究旨在探讨升麻素苷对脂多糖(LPS)刺激的RAW 264.7巨噬细胞的抗炎作用。

材料与方法

采用细胞计数试剂盒-8法检测细胞活力。通过酶联免疫吸附测定法评估一氧化氮(NO)、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和IL-6的产生。分别进行实时聚合酶链反应和蛋白质印迹分析mRNA和蛋白质水平。

结果

在整个实验过程中,15、50和100μg/mL的升麻素苷对RAW 264.7细胞无细胞毒性。升麻素苷剂量依赖性地抑制LPS诱导的NO、TNF-α、IL-1β和IL-6的产生。升麻素苷处理以浓度依赖性方式下调LPS激活的RAW 264.7巨噬细胞中诱导型NO合酶(iNOS)和环氧化酶2(COX-2)的mRNA和蛋白质表达。此外,升麻素苷处理可防止RAW 264.7巨噬细胞中LPS诱导的JAK2/STAT3激活。STAT3过表达显著逆转了升麻素苷对LPS激活的RAW 264.7巨噬细胞的作用。

结论

这些结果表明,升麻素苷通过抑制JAK2/STAT3磷酸化来抑制iNOS和COX-2表达,从而发挥抗炎作用。

总结

升麻素苷通过抑制JAK2/STAT3信号传导来抑制iNOS和COX-2表达,从而在RAW 264.7巨噬细胞中发挥抗炎作用。LPS:脂多糖;NO:一氧化氮;TNF-α:肿瘤坏死因子-α;IL:白细胞介素;RS:防风;POG:升麻素苷;iNOS:诱导型NO合酶;COX2:环氧化酶;FBS:胎牛血清;DMSO:二甲基亚砜;CCK-8:细胞计数试剂盒;RIPA:放射免疫沉淀测定缓冲液;ECL:增强化学发光;SD:标准差;ELISA:酶联免疫吸附测定

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c1/5551353/6be55e258711/PM-13-378-g001.jpg

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