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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >HO-1 Induction by Selaginella tamariscina Extract Inhibits Inflammatory Response in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages
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HO-1 Induction by Selaginella tamariscina Extract Inhibits Inflammatory Response in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages

机译:卷柏卷柏提取物的HO-1诱导抑制脂多糖刺激的RAW 264.7巨噬细胞的炎症反应。

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Selaginella Herba is the dried, aerial part of Selaginella tamariscina (P.Beauv.) Spring and has been used to treat amenorrhea, abdominal pain, headaches, and hematuria in Korea. However, scientific evidence regarding the anti-inflammatory activity and action mechanism of Selaginella tamariscina is lacking. Thus, the present study was performed to investigate the anti-inflammatory and antioxidant activities of Selaginella tamariscina ethanol extract (STE) against lipopolysaccharide (LPS)-induced inflammatory responses and identify the molecular mechanism responsible. STE was prepared by heating in 70% ethanol and its quality was confirmed by HPLC. STE dose-dependently inhibited the productions of inflammatory mediators (NO and PGE2) and proinflammatory cytokines (IL-1β and IL-6) in LPS-stimulated RAW 264.7 cells. STE markedly suppressed the phosphorylations of MAPKs, IκB-α, and NF-κB and the nuclear translocation of NF-κB induced by LPS stimulation. In addition, STE exhibited good free radical scavenging activity and prevented ROS generation by LPS. STE also upregulated the expression of Nrf2 and HO-1 and promoted the nuclear translocation of Nrf2. Taken together, STE was found to have anti-inflammatory and antioxidant effects on RAW 264.7 macrophages and the mechanism appeared to involve the MAPK, NF-κB, and Nrf2/HO-1 signaling pathways. These results suggest that STE might be useful for preventing or treating inflammatory diseases and provide scientific evidence that supports the developments of herbal prescriptions or novel natural products.
机译:卷柏(Selaginella Herba)是卷柏卷柏(P.Beauv。)春季干燥的空中部分,在韩国已被用于治疗闭经,腹痛,头痛和血尿。然而,缺乏关于卷柏卷柏的抗炎活性和作用机制的科学证据。因此,本研究旨在研究卷柏卷柏乙醇提取物(STE)对脂多糖(LPS)诱导的炎症反应的抗炎和抗氧化活性,并确定引起该反应的分子机制。通过在70%乙醇中加热来制备STE,并通过HPLC确认其质量。 STE剂量依赖性地抑制LPS刺激的RAW 264.7细胞中炎性介质(NO和PGE2)和促炎细胞因子(IL-1β和IL-6)的产生。 STE显着抑制LPS刺激诱导的MAPK,IκB-α和NF-κB的磷酸化以及NF-κB的核易位。此外,STE表现出良好的自由基清除活性,并防止LPS产生ROS。 STE还上调Nrf2和HO-1的表达并促进Nrf2的核易位。综上所述,STE被发现对RAW 264.7巨噬细胞具有抗炎和抗氧化作用,其机制似乎涉及MAPK,NF-κB和Nrf2 / HO-1信号通路。这些结果表明,STE可能对预防或治疗炎性疾病有用,并提供了支持草药处方或新型天然产物发展的科学证据。

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