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首页> 外文期刊>Journal of natural products >Inhibition of NF- kappa B activation and iNOS induction by ent-kaurane diterpenoids in LPS-stimulated RAW264.7 murine macrophages.
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Inhibition of NF- kappa B activation and iNOS induction by ent-kaurane diterpenoids in LPS-stimulated RAW264.7 murine macrophages.

机译:LPS刺激的RAW264.7鼠巨噬细胞中 ent -贝壳杉烷二萜类化合物对NF-κB活化的抑制和iNOS的诱导。

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摘要

Xerophilusin A (1), xerophilusin B (2), longikaurin B (3), and xerophilusin F (4) from Isodon xerophylus inhibit LPS-induced NO production in RAW 264.7 macrophages, with IC50 values of 0.60, 0.23, 0.44, and 0.67 micro M, respectively, and they all inhibited mRNA production in these same cells. They decreased the luciferase activity in RAW 264.7 cells transiently transfected with the NF- kappa B-dependent luciferase reporter, with IC50 values of 1.8, 0.7, 1.2, and 1.6 micro M, respectively. Compounds 1-3 reduced NF- kappa B activation, with compound 4 showing no effect, but p65 translocation from the cytoplasm to the nucleus and the LPS-induced degradation of I kappa B were inhibited by all four test compounds. These findings indicate that ent-kauranes are potential anti-inflammatory agents, with a specific mechanism in which both the inhibition of NF- kappa B translocation and the consequent decrease of pro-inflammatory mediators are implicated.
机译:Xerodonus xi。的Xerophilusin A(1),Xerophilusin B(2),longikaurin B(3)和Xerophilusin F(4)抑制LPS诱导的RAW 264.7巨噬细胞中NO的产生,IC 50 值分别为0.60、0.23、0.44和0.67 micro M,它们都抑制了这些相同细胞中的mRNA产生。他们降低了瞬时转染了NF-κB依赖的荧光素酶报告基因的RAW 264.7细胞中的荧光素酶活性,IC <50>分别为1.8、0.7、1.2和1.6 microM。化合物1-3降低了NF-κB的活化,化合物4没有作用,但是所有四种受试化合物均抑制了p65从细胞质到细胞核的易位和LPS诱导的IκB的降解。这些发现表明, ent -呋喃酮是潜在的抗炎药,具有特定的机制,其中涉及抑制NF-κB易位和随之而来的促炎介质的减少。

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