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Influence of cytokine inhibitors on concentration and activity of MMP-1 and MMP-3 in disc herniation

机译:细胞因子抑制剂对椎间盘突出症中MMP-1和MMP-3的浓度和活性的影响

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Introduction Spontaneous resorption of disc herniation (DH) after sciatica is well documented. The matrix metalloproteinases (MMP)-1 and MMP-3 are enzymes potentially involved in this process. Glucocorticoid injections are commonly used for treatment, and other anti-inflammatory molecules like tumor necrosis factor (TNF) inhibitors are under clinical investigation. However, little is known about the effect of these molecules on DH resorption. Methods DH tissue was harvested from patients undergoing surgery for sciatica. Samples were thoroughly washed. Diced explants were cultured ex-vivo in 1) 0.5 ml Dulbecco's modified Eagle's medium (DMEM) 10% fetal calf serum (FCS), (controls), 2) recombinant interleukin 1 receptor antagonist (IL-1Ra), (100 ng/ml), 3) dexamethasone (10E-5 M), or 4) TNF inhibitor monoclonal antibody (10 μg/ml). Supernatants were harvested at 48 hours and frozen. Immunocapture activity assays determined total MMP activity, active MMP levels and pro-MMP levels. Results Fourteen DH tissue samples were analysed. Levels of all forms of MMP-3 were higher than the respective levels of MMP-1( P < 0.01). In particular, the median (interquartile range [IQR]) total MMP-3 level was 0.97 (0.47 - 2.19) ng/mg of tissue compared to 0.024 (0.01 - 0.07) ng/mg of total MMP-1 level ( P < 0.01). Incubation with IL-1Ra, dexamethasone, or TNF inhibitors significantly decreased levels of all forms of MMP-3 ( P < 0.05). Dexamethasone significantly decreased the ratio of active MMP-3 to total MMP-3 activity. A significant inhibitory effect of dexamethasone was observed only on active MMP-1, while IL-1 and TNF inhibitor had no significant effect on any form. Conclusions MMP-3 appears to play a greater role than MMP-1 in DH resorption. Dexamethasone, IL-1-Ra and TNF inhibitor decreased active MMP-3, indicating that the clinical use of these drugs may affect the resorption of DH under certain conditions.
机译:简介坐骨神经痛后自发性椎间盘突出症(DH)吸收已有文献报道。基质金属蛋白酶(MMP)-1和MMP-3是可能参与此过程的酶。糖皮质激素注射剂通常用于治疗,其他抗炎分子如肿瘤坏死因子(TNF)抑制剂正在临床研究中。然而,关于这些分子对DH吸收的影响知之甚少。方法从坐骨神经痛手术患者中收集DH组织。样品被彻底清洗。将切成丁的外植体在1)0.5 ml Dulbecco改良的Eagle培养基(DMEM),10%胎牛血清(FCS),2)重组白介素1受体拮抗剂(IL-1Ra)(100 ng / ml)中离体培养),3)地塞米松(10E-5 M)或4)TNF抑制剂单克隆抗体(10μg/ ml)。在48小时时收获上清液并冷冻。免疫捕获活性测定确定了总MMP活性,活性MMP水平和pro-MMP水平。结果共分析了14个DH组织样本。所有形式的MMP-3的水平均高于各自的MMP-1的水平(P <0.01)。特别是,MMP-3总水平的中位数(四分位数范围[IQR])为0.97(0.47-2.19)ng / mg,而MMP-1总水平的平均值为0.024(0.01-0.07)ng / mg(P <0.01 )。与IL-1Ra,地塞米松或TNF抑制剂一起孵育可显着降低所有形式的MMP-3的水平(P <0.05)。地塞米松显着降低了活性MMP-3与总MMP-3活性的比率。仅在活性MMP-1上观察到地塞米松的显着抑制作用,而IL-1和TNF抑制剂对任何形式均无显着​​影响。结论MMP-3在DH吸收中似乎比MMP-1发挥更大的作用。地塞米松,IL-1-Ra和TNF抑制剂可降低活性MMP-3,表明这些药物的临床使用可能会在某些条件下影响DH的吸收。

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