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首页> 外文期刊>International immunopharmacology >Isodeoxyelephantopin, a sesquiterpene lactone from Elephantopus scaber Linn., inhibits pro-inflammatory mediators' production through both NF-kappa B and AP-1 pathways in LPS-activated macrophages
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Isodeoxyelephantopin, a sesquiterpene lactone from Elephantopus scaber Linn., inhibits pro-inflammatory mediators' production through both NF-kappa B and AP-1 pathways in LPS-activated macrophages

机译:来自elephantopus scaber linn的倍二萜内酯的异氧基丙酮,抑制了通过LPS-活化的巨噬细胞的NF-Kappa B和AP-1途径的促进炎症介质的生产

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摘要

Isodeoxyelephantopin (IDET) has been identified as an anti-tumor natural constituent whose anti-tumor activity and mechanism have been widely investigated. Since the occurrence and development of cancer usually accompany with inflammation, and tumor signaling shares many components with inflammation signaling, the agents with anti-tumor activity are likely to possess anti-inflammation potential. Thus, the current study aims to demonstrate the anti-inflammatory activity along with the underlying mechanism of IDET in lipopolysaccharide (LPS)-primed macrophages. By using Griess method and ELISA, we found that in both bone marrow derived macrophages and alveolar macrophage cell line, IDET, at relatively low concentrations (0.75, 1.5 and 3 mu M), could inhibit LPS-induced expression of various pro-inflammatory mediators including nitric oxide (NO) generated by inducible nitric oxide synthase (iNOS), interleukin (IL)-6, monocyte chemotactic protein-1 (MCP-1) and IL-1 beta. Meanwhile, in activated MH-S cells, the inhibitory action of IDET on mRNA expression levels of these cytokines was also detected using qPCR. Mechanistically, the effects of IDET on two key inflammatory signalings, nuclear factor-kappa B (NF-kappa B) and activator protein-1 (AP-1) pathways, were determined in LPS-activated MH-S cells by reporter gene along with western blot assays. On the one hand, IDET suppressed NF-kappa B signaling via down-regulating phosphorylation and degradation of inhibitor of NF-kappa B (I kappa B)-alpha and the subsequent p65 translocation. On the other hand, IDET dampened AP-1 signaling through attenuating phosphorylation of both c-jun N-terminal kinase 1/2 (JNK1/2) and extracellular signal regulated kinase 1/2 (ERK1/2). Our study indicates that IDET might be a promising constituent from the anti-inflammatory herb Elephantopus scaber Linn. in mitigating inflammatory conditions, especially respiratory inflammation.
机译:异氧基骨肽(IDET)已被鉴定为抗肿瘤天然成分,其抗肿瘤活性和机制已被广泛研究。由于癌症的发生和发展通常伴随着炎症,并且肿瘤信号传导与炎症信号传导共享许多组分,因此具有抗肿瘤活性的试剂可能具有抗炎潜力。因此,目前的研究旨在证明抗炎活动以及IDET在脂多糖(LPS) - 预期巨噬细胞中的潜在机制。通过使用GRIESS方法和ELISA,发现在两个骨髓衍生的巨噬细胞和肺泡巨噬细胞系中,IDET,在相对低的浓度(0.75,1.5和3μm),可以抑制LPS诱导的各种促炎介质的表达包括由诱导型一氧化氮合酶(InOS)产生的一氧化氮(NO),白细胞介素(IL)-6,单核细胞趋化蛋白-1(MCP-1)和IL-1β。同时,在活化的MH-S细胞中,使用QPCR检测IET对这些细胞因子的mRNA表达水平的抑制作用。通过报告基因在LPS激活的MH-S细胞中,通过报告基因以及REPS-活化的MH-S细胞,测定IET对两个关键炎症信号,核因子-Kappa B)和活化剂蛋白-1(AP-1)途径的影响。 Western印迹测定。一方面,IDET通过下调NF-Kappa B(IκB)-alpha和随后的P65易位的抑制剂的磷酸化和降解NF-Kappa B信号传导。另一方面,IDET通过衰减C-JUN N-末端激酶1/2(JNK1 / 2)和细胞外信号调节激酶1/2(ERK1 / 2)的磷酸化通过衰减磷酸化,通过衰减AP-1信号传导。我们的研究表明,IDET可能是来自抗炎药草eLephantopus scaber Linn的有前途的成分。在减轻炎症条件下,尤其是呼吸炎症。

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