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首页> 外文期刊>Clinical and experimental rheumatology >Selective iNOS inhibitor 1400W enhances anti-catabolic IL-10 and reduces destructive MMP-10 in OA cartilage. Survey of the effects of 1400W on inflammatory mediators produced by OA cartilage as detected by protein antibody array.
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Selective iNOS inhibitor 1400W enhances anti-catabolic IL-10 and reduces destructive MMP-10 in OA cartilage. Survey of the effects of 1400W on inflammatory mediators produced by OA cartilage as detected by protein antibody array.

机译:选择性iNOS抑制剂1400W增强OA软骨中的抗分解IL-10并降低破坏性MMP-10。用蛋白抗体阵列检测1400W对OA软骨产生的炎症介质的影响。

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OBJECTIVES:In osteoarthritis (OA), the balance between catabolic and anabolic mediators and their regulators in cartilage is disturbed. Proinflammatory cytokine interleukin-1 (IL-1) plays a central role in cartilage destruction and nitric oxide (NO) mediates many of its destructive effects. In the present study, we investigated the secretion of 40 mediators related to inflammation or cartilage degradation by OA cartilage samples with a protein antibody array. The effects of IL-1 and a selective iNOS-inhibitor 1400W on the mediator release were also studied.METHODS:Cartilage tissue was obtained from the leftover pieces of total knee replacement surgery from OA patients. Protein antibody array was used to measure production of 40 mediators in the culture medium. ELISA was used to confirm the antibody array results.RESULTS:OA cartilage secreted spontaneously 15 out of the 40 measured mediators. IL-1Beta enhanced production of 11 of these inflammatory mediators in OA cartilage along with increased NO production. Treatment with a selective iNOS inhibitor 1400W enhanced the production of IL-10, while the levels of MMP-10 were reduced in IL-1 -treated OA cartilage.CONCLUSION:OA cartilage produces many of the mediators involved in the pathogenesis of OA. The ability of 1400W to enhance levels of anti-catabolic IL-10 and to reduce levels of destructive MMP-10 points to the anti-inflammatory mechanisms that iNOS-inhibitors may have.
机译:目的:在骨关节炎(OA)中,分解代谢和合成代谢介质及其在软骨中的调节剂之间的平衡受到干扰。促炎细胞因子白介素-1(IL-1)在软骨破坏中起核心作用,而一氧化氮(NO)介导其许多破坏作用。在本研究中,我们调查了具有蛋白质抗体阵列的OA软骨样品中与炎症或软骨降解相关的40种介体的分泌。还研究了IL-1和选择性iNOS抑制剂1400W对介质释放的影响。方法:软骨组织取自OA患者的全膝关节置换手术的剩余部分。蛋白抗体阵列用于测量培养基中40种介体的产生。结果:40种被测介体中,OA软骨自发分泌15种。 IL-1Beta增强了OA软骨中11种炎症介质的产生,并增加了NO的产生。选择性iNOS抑制剂1400W处理可提高IL-10的产生,而IL-1处理的OA软骨中MMP-10的水平会降低。结论:OA软骨产生了许多与OA发病有关的介体。 1400W增强抗催化IL-10水平和降低破坏性MMP-10水平的能力指向iNOS抑制剂可能具有的抗炎机制。

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