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首页> 外文期刊>Inflammopharmacology >Combined atorvastatin and pentoxifylline in ameliorating inflammation induced by complete Freund's adjuvant
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Combined atorvastatin and pentoxifylline in ameliorating inflammation induced by complete Freund's adjuvant

机译:阿托伐他汀和己酮可可碱联合治疗完全弗氏佐剂诱导的炎症

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Injection of complete Freund's adjuvant (CFA) into one of the footpads of Wistar rats promotes swelling in all the footpads (including non-injected footpads) in the next few days, indicating a complicated immunological reaction and autoimmune arthritis. This survey was performed to assess the synergistic benefits of combined atorvastatin and pentoxifylline for treating arthritis induced by CFA. Therapeutic regimes began on day 12 post-challenge when all the rats recorded an arthritis index of more than one and continued throughout the investigation until day 32. Treatment with combined atorvastatin and pentoxifylline at half doses led to synergistic benefits causing the regression of clinical and radiological appearance of arthritis in non-injected paws, which was more favorable than treatment with any medication alone at full doses. Moreover, the combined treatment led to a reduction in some inflammatory biochemical parameters, such as myeloperoxidase, nitric oxide, and C-reactive protein, which was more pronounced than those of the treatment with each medication alone. The mRNA expression of IL-1 beta and TNF-alpha in the rat toe area was significantly decreased by combination therapy, and this reduction was more significant than that of monotherapy. The ratios of ROR gamma c/T-bet, ROR gamma c/GATA-3, RoR gamma c/Foxp3, T-bet/GATA-3, and T-bet/Foxp3 expression showed a further decrease in the combined treated group compared to other groups. Interestingly, combination therapy did not reduce T lymphocyte proliferation to a level lower than healthy rats. Overall, the combination of atorvastatin and pentoxifylline possesses immunomodulatory synergistic benefits, and this approach may be an impressive strategy to manage complicated inflammation.
机译:在接下来的几天内,将完全弗氏佐剂(CFA)注射到Wistar大鼠的一个脚垫中会促进所有脚垫(包括未注射的脚垫)的肿胀,表明复杂的免疫反应和自身免疫性关节炎。本调查旨在评估阿托伐他汀和己酮可可碱联合治疗 CFA 诱导的关节炎的协同作用。治疗方案从攻击后第12天开始,当时所有大鼠的关节炎指数都超过1,并在整个调查过程中持续到第32天。半剂量的阿托伐他汀和己酮可可碱联合治疗可产生协同效应,导致非注射爪关节关节炎的临床和放射学表现消退,这比单独使用任何药物治疗更有利。此外,联合治疗导致一些炎症生化参数的降低,如髓过氧化物酶、一氧化氮和C反应蛋白,这比单独使用每种药物治疗更明显。联合治疗大鼠脚趾区IL-1β和TNF-α的mRNA表达显著降低,且比单药治疗更显著。与其他组相比,联合治疗组的RORγ c/T-bet、ROR γ c/GATA-3、RoR γ c/Foxp3、T-bet/GATA-3和T-bet/Foxp3表达的比值进一步降低。有趣的是,联合治疗并没有将T淋巴细胞增殖降低到低于健康大鼠的水平。总体而言,阿托伐他汀和己酮可可碱的联合治疗具有免疫调节协同作用,这种方法可能是治疗复杂炎症的令人印象深刻的策略。

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