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Inhibitory Actions of Tetrandrine on Tumor Necrosis Factor α-Induced NF-κB Activation in Neovascularization of Cultured Choroidal Explants

机译:粉防己碱对脉络膜外植体新生血管形成中肿瘤坏死因子α诱导的NF-κB活化的抑制作用。

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Tetrandrine (1 μM), a bis-benzylisoquinoline alkaloid isolated from Stephania tetrandra S Moore, signifi-cantly decreased tumor necrosis factor alpha (TNFα; 10 ng/ml)-induced increase in the number of micro vessels that budded from cultured rat choroidal explants. Tetrandrine also decreased the TNFα-induced in-crease in the number of cells composing the microvessels. Ammonium pyrrolidine dithiocarbamate (APDC; 0.1-0.3 μM), an inhibitor of nuclear factor-κB (NF-κB), decreased the TNFα-induced increase in the number of microvessels in a concentration-dependent manner. TNFα increased the phosphorylation and degradation of inhibitor of NF-κB (IκBα), as well as increasing the DNA-binding activity of NF-κB in choroidal explants. TNF? induced an increase of vascular endothelial growth factor (VEGF)-A mRNA, but not VEGF-C mRNA or VEGF-D mRNA. TNFα-induced angiogenic action was inhibited by treatment of VEGF-A antibody in cultured choroidal capillaries. Tetrandrine inhibited the TNFα-induced increases of phosphorylation and degradation of IκBα, and reduced the TNFα-induced increase of DNA-binding activity of NF-κB in chor-oidal explants. In conclusion, tetrandrine inhibits TNFα-induced activation of NF-κB in the choroidal capil-laries via inhibition of TNFα-induced phosphorylation of IκBα.
机译:粉防己碱(1μM)是从Stephania tetrandra S Moore中分离出的双苄基异喹啉生物碱,可显着减少肿瘤坏死因子α(TNFα; 10 ng / ml)诱导的从培养的大鼠脉络膜外植体发芽的微血管数量增加。粉防己碱还减少了TNFα诱导的组成微血管的细胞数量的增加。吡咯烷二硫代氨基甲酸铵(APDC; 0.1-0.3μM)是一种核因子-κB(NF-κB)抑制剂,以浓度依赖的方式降低了TNFα诱导的微血管数量增加。 TNFα增强了NF-κB抑制剂(IκBα)的磷酸化和降解,并增加了脉络膜外植体中NF-κB的DNA结合活性。肿瘤坏死因子诱导血管内皮生长因子(VEGF)-A mRNA升高,但不诱导VEGF-C mRNA或VEGF-D mRNA升高。通过在培养的脉络膜毛细血管中处理VEGF-A抗体可抑制TNFα诱导的血管生成作用。粉防己碱可以抑制TNFα诱导的IκBα磷酸化和降解的增加,并降低TNFα诱导的类脉外植体NF-κBDNA结合活性的增加。总之,粉防己碱通过抑制TNFα诱导的IκBα磷酸化,抑制TNFα诱导的脉络膜毛细血管中NF-κB的活化。

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