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Ugonin M, a Helminthostachys zeylanica Constituent, Prevents LPS-Induced Acute Lung Injury through TLR4-Mediated MAPK and NF-κB Signaling Pathways

机译:Ugonin M是一种Helminthostachys zeylanica成分,可通过TLR4介导的MAPK和NF-κB信号传导途径预防LPS诱导的急性肺损伤

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Helminthostachys zeylanica (L.) Hook. is plant that has been used in traditional Chinese medicine for centuries for the treatment of inflammation, fever, pneumonia, and various disorders. The aims of the present study are to figure out the possible effectiveness of the component Ugonin M, a unique flavonoid isolated from H. zeylanica , and to elucidate the mechanism(s) by which it works in the LPS-induced ALI model. In this study, Ugonin M not only inhibited the production of pro-inflammatory mediators such as NO, TNF-α, IL-1β, and IL-6, as well as infiltrated cellular counts and protein content in the bronchoalveolar lavage fluid (BALF) of lipopolysaccharides (LPS)-induced acute lung injury (ALI) mice, but also ameliorated the severity of pulmonary edemas through the score of a histological examination and the ratio of wet to dry weight of lung. Moreover, Ugonin M was observed to significantly suppress LPS-stimulated protein levels of iNOS and COX-2. In addition, we found that Ugonin M not only obviously suppressed NF-κB and MAPK activation via the degradation of NF-κB and IκB-α as well as ERK and p38MAPK active phosphorylation but also inhibited the protein expression level of TLR4. Further, Ugonin M treatment also suppressed the protein levels of MPO and enhanced the protein expressions of HO-1 and antioxidant enzymes (SOD, GPx, and CAT) in lung tissue of LPS-induced ALI mice. It is anticipated that through our findings, there is strong evidence that Ugonin M may exert a potential effect against LPS-induced ALI mice. Hence, Ugonin M could be one of the major effective components of H. zeylanica in the treatment of inflammatory disorders.
机译:Helminthostachys zeylanica(L.)钩。是在传统中药中使用了几个世纪的植物,用于治疗炎症,发烧,肺炎和各种疾病。本研究的目的是弄清组分Ugonin M的可能效力,Ugonin M是从玉米中分离出的独特类黄酮,并阐明了它在LPS诱导的ALI模型中起作用的机制。在这项研究中,Ugonin M不仅抑制了促炎性介质(如NO,TNF-α,IL-1β和IL-6)的产生,还抑制了支气管肺泡灌洗液(BALF)中浸润的细胞数量和蛋白质含量。脂多糖(LPS)诱导的急性肺损伤(ALI)小鼠的体重减轻,但也可以通过组织学检查得分和肺干湿比来改善肺水肿的严重程度。此外,观察到Ugonin M可显着抑制LPS刺激的iNOS和COX-2蛋白水平。此外,我们发现Ugonin M不仅通过NF-κB和IκB-α的降解以及ERK和p38MAPK的活性磷酸化明显抑制NF-κB和MAPK的活化,而且还抑制了TLR4的蛋白表达水平。此外,Ugonin M处理还可以抑制LPS诱导的ALI小鼠肺组织中MPO的蛋白质水平,并增强HO-1和抗氧化酶(SOD,GPx和CAT)的蛋白质表达。可以预料,通过我们的发现,有充分的证据表明Ugonin M可能对LPS诱导的ALI小鼠发挥潜在作用。因此,Ugonin M可能是zeylanica炎性疾病治疗的主要有效成分之一。

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