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首页> 外文期刊>Molecular medicine reports >Dipterocarpus obtusifolius attenuates the effects of lipopolysaccharide-induced inflammatory response in RAW264.7 macrophages
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Dipterocarpus obtusifolius attenuates the effects of lipopolysaccharide-induced inflammatory response in RAW264.7 macrophages

机译:Dipterocarpus obsusifolius衰减Raw264.7巨噬细胞脂多糖诱导的炎症反应的影响

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摘要

Dipterocarpus obtusifolius has been traditionally used as a herbal medicine and is considered to have anticancer properties. The biological activity of D. obtusifolius in inflammation and the underlying mechanisms of its activity remain to be elucidated. The present study investigated the effects of D. obtusifolius methanolic extract (DOME) on lipopolysaccharide (LPS)-stimulated inflammation in RAW264.7 cells. The effects of DOME on the production of nitric oxide, prostaglandin E-2 and pro-inflammatory cytokines were assessed by ELISA, western blot analysis and reverse transcription-quantitative polymerase chain reaction. It was demonstrated that expression of inducible nitric oxide synthase, cyclooxygenase-2, interleukin-1 beta and tumor necrosis factor-a was suppressed by DOME in LPS-stimulated cells. Furthermore, treatment with DOME suppressed phosphorylation of mitogen activated protein kinase (MAPK) molecules, including extracellular signal-regulated kinase, c-Jun N-terminal kinase and p38 MAPK. Translocation of the nuclear factor-kappa B p65 subunit into the nucleus was additionally inhibited by DOME. Phosphorylation of MAPK promoter activity was inhibited by treatment with DOME, PD98059, SB202190 and SP600125. These results demonstrated that DOME inhibits LPS-induced inflammatory responses. Therefore, DOME may be a potential therapeutic approach for the treatment of inflammatory diseases.
机译:Dipterocarpus obsusifolius传统上用作草药,被认为具有抗癌性质。 D.凋亡的生物活性炎症和其活性的潜在机制仍然阐明。本研究研究了D.Topusifolius甲醇提取物(圆顶)对Raw264.7细胞中脂多糖(LPS)刺激的炎症的影响。通过ELISA,Western印迹分析和逆转录定量聚合酶链反应评估圆顶对一氧化氮,前列腺素E-2和促炎细胞因子的影响。结果表明,LPS刺激细胞中的圆顶抑制了诱导型一氧化氮合酶,环氧氧酶-2,白细胞介素-1β和肿瘤坏死因子-A的表达。此外,用圆顶抑制介质活性蛋白激酶(MAPK)分子的磷酸化,包括细胞外信号调节激酶,C-JUN N-末端激酶和P38MAPK。圆顶还抑制了核因子-Kappa B p65亚基的旋律序列。用圆顶,PD98059,SB202190和SP600125处理抑制MAPK启动子活性的磷酸化。这些结果表明,圆顶抑制LPS诱导的炎症反应。因此,圆顶可能是治疗炎症性疾病的潜在治疗方法。

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