首页> 外文期刊>The Journal of rheumatology >FK506 attenuates developing and established joint inflammation and suppresses interleukin 6 and nitric oxide expression in bacterial cell wall induced polyarthritis.
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FK506 attenuates developing and established joint inflammation and suppresses interleukin 6 and nitric oxide expression in bacterial cell wall induced polyarthritis.

机译:FK506在细菌细胞壁诱发的多关节炎中减轻发展中的关节炎症并抑制白介素6和一氧化氮的表达。

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OBJECTIVE: To determine the efficacy of therapeutic administration of FK506 (Tacrolimus) in suppressing developing and established joint inflammation, proinflammatory cytokine expression, and nitric oxide (NO) production in peptidoglycan-polysaccharide (PG/PS) induced experimental polyarthritis in rats. METHODS: Chronic joint inflammation was induced by intraperitoneal injection of PG/PS, and joint inflammation was quantified using arthritis index and paw volume. Serum and joint levels of interleukin 6 (IL-6) were measured by bioassay and Western blot analysis respectively, and serum levels of NO production were determined by the Griess procedure and the expression of the inducible isoform of nitric oxide synthase (i-NOS) in the joints was determined by Western blot analysis. RESULTS: Arthritis induced by PG/PS is biphasic, progressing through an initial acute phase and a remission phase, which is followed by a persistent chronic phase. Daily administration of FK506 initiated during the remission phase significantly attenuated the onset and development of chronic joint inflammation. We observed a significant reduction in joint inflammation and swelling, an apparent suppression of pannus development, and minimal erosive damage to the articular cartilage and subchondral bone. Fully established chronic joint inflammation was also ameliorated by daily administration of FK506. Joint swelling and inflammation was significantly reduced by 5 days post-treatment with FK506 and the erosive activity associated with the pannus appeared diminished. The elevated expression of IL-6 and NO characteristic of chronic joint inflammation in the serum and in joint tissue was significantly reduced by FK506 treatment. CONCLUSION: Therapeutic administration of FK506 has a profound antiinflammatory effect on the development of the chronic, erosive arthritis induced by PG/PS. This attenuation in joint inflammation was associated with suppression of IL-6 and NO production systemically and locally in the joints. Our data suggest that FK506 may be effective in the treatment of chronic joint inflammation associated with rheumatoid arthritis.
机译:目的:确定治疗性应用FK506(他克莫司)抑制肽聚糖多糖(PG / PS)诱发的实验性多关节炎的发展中和已确立的关节炎症,促炎性细胞因子表达和一氧化氮(NO)生成的功效。方法:腹膜内注射PG / PS可诱发慢性关节发炎,并通过关节炎指数和足爪体积量化关节发炎。分别通过生物测定和蛋白质印迹分析测量血清和关节白介素6(IL-6)的水平,并通过Griess程序和一氧化氮合酶(i-NOS)的诱导型亚型的表达确定血清NO的产生水平通过蛋白质印迹分析确定关节中的蛋白。结果:PG / PS诱发的关节炎是双相性的,进展为初始急性期和缓解期,随后为持续性慢性期。在缓解期开始的FK506每日给药显着减轻了慢性关节炎症的发作和发展。我们观察到关节炎症和肿胀明显减少,血管pan发育明显受到抑制,对关节软骨和软骨下骨的侵蚀性损害最小。每天服用FK506也可改善完全确立的慢性关节发炎。用FK506治疗后5天,关节肿胀和炎症显着减少,与血管nu相关的糜烂活性似乎减弱了。 FK506处理可显着降低血清和关节组织中IL-6的表达升高和慢性关节炎症的NO特征。结论:FK506的治疗性给药对PG / PS诱发的慢性糜烂性关节炎的发展具有深远的消炎作用。关节炎症的这种减弱与全身和局部抑制IL-6和NO产生有关。我们的数据表明FK506可能有效治疗与类风湿关节炎有关的慢性关节发炎。

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