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Anti-Inflammatory Activities of Biapigenin Mediated by Actions on p38 MAPK Pathway

机译:通过对p38 MAPK途径的作用介导的Biapigenin的抗炎活性

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摘要

Biapigenin is a naturally occurring biflavonoid found in Selaginella tamariscina. This study aimed to investigate the anti-inflammatory activity of biapigenin and its mechanisms of action, and to identify possible target proteins. Biapigenin suppressed nitric oxide (NO) production, as well as tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and macrophage inflammatory protein (MIP)-2 cytokine release. Moreover, biapigenin completely inhibited IL-1 beta, inducible nitric oxide synthases (iNOS), and MIP-2 mRNA expression and partially suppressed MIP-1 and TNF-alpha expression. Lipopolysaccharide (LPS)-induced upregulation of p38 mitogen-activated protein kinase (MAPK) phosphorylation was significantly reduced by biapigenin. Fluorescence titration experiment revealed that biapigenin bound to p38 with a high binding affinity of 2.57 x 10(6) M-1. These results suggest that biapigenin demonstrates anti-inflammatory activities by the regulation of phosphorylation of p38 MAPK pathway. Our results strongly suggest that biapigenin may be a potent biflavonoid inhibitor of p38 MAPK and have therapeutic applications in the treatment of inflammatory diseases.
机译:Biapigenin是天然存在的双黄酮,存在于卷柏卷柏中。这项研究旨在调查Biapigenin的抗炎活性及其作用机理,并确定可能的靶蛋白。 Biapigenin抑制一氧化氮(NO)的产生,以及肿瘤坏死因子(TNF)-α,白介素(IL)-1 beta和巨噬细胞炎性蛋白(MIP)-2细胞因子的释放。此外,biapigenin完全抑制IL-1β,诱导型一氧化氮合酶(iNOS)和MIP-2 mRNA表达,并部分抑制MIP-1和TNF-α表达。 Biapigenin可显着减少脂多糖(LPS)诱导的p38丝裂原活化蛋白激酶(MAPK)磷酸化的上调。荧光滴定实验表明,联芹黄素以2.57 x 10(6)M-1的高结合亲和力与p38结合。这些结果表明联芹黄素通过调节p38 MAPK途径的磷酸化表现出抗炎活性。我们的结果有力地表明,联芹黄素可能是p38 MAPK的有效双黄酮类抑制剂,并在炎性疾病的治疗中具有治疗应用。

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