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首页> 外文期刊>International immunopharmacology >Alginic acid isolated from Sargassum wightii exhibits anti-inflammatory potential on type II collagen induced arthritis in experimental animals
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Alginic acid isolated from Sargassum wightii exhibits anti-inflammatory potential on type II collagen induced arthritis in experimental animals

机译:从Wargari(Sargassum wightii)分离出来的藻酸对实验动物的II型胶原诱导的关节炎具有抗炎作用

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摘要

The present study evaluated the anti-inflammatory potential of alginic acid isolated from the brown algae Sargassum wightii in type II collagen induced arthritic rats, a well established arthritic model that resembles more closely to human rheumatoid arthritis in its clinical, pathological, immunological and histological aspects. Type II collagen induced arthritic rats showed increased activities of inflammatory marker enzymes like cycloxygenase-2 (COX-2), lipoxygenase (5-LOX), xanthine oxidase (XO) and myeloperoxidase (MPO) along with increased concentration of rheumatoid factor (RF), ceruloplasmin and C-reactive protein (CRP). Treatment with alginic acid significantly reduced the activities of COX-2 and 5-LOX along with reduction in MPO, XO, RF and CRP. Alginic acid treatment reverted to the altered levels of hematological parameters like RBC count, WBC count and ESR in arthritic rats. Concentrations of proinflammatory cytokines like IL-1 β, TNF α and IL-6 were significantly higher in arthritic rats which were reduced on treatment with alginic acid. Increased activities of lysosomal enzymes that manifest the systemic damage during arthritis were significantly reduced by the treatment with alginic acid which indicates the reduction in the rupture and degradation of connective tissue. Histopathology of knee joint tissues showed that extensive bone degradation and synovial hyperplasia along with infiltrating cells and treatment with alginic acid reversed the histopathological changes which indicate the protective potential of alginic acid in rheumatoid arthritis.
机译:本研究评估了从褐藻海藻Sargassum wightii中分离出的藻酸在II型胶原诱导的关节炎大鼠中的能力,这是一种成熟的关节炎模型,在临床,病理,免疫学和组织学方面与人类风湿性关节炎更为相似。 II型胶原诱导的关节炎大鼠显示出炎症标记酶(如环氧合酶2(COX-2),脂氧合酶(5-LOX),黄嘌呤氧化酶(XO)和髓过氧化物酶(MPO)的活性增加,以及类风湿因子(RF)的浓度增加,铜蓝蛋白和C反应蛋白(CRP)。用藻酸处理显着降低了COX-2和5-LOX的活性,同时降低了MPO,XO,RF和CRP。海藻酸治疗可恢复关节炎大鼠血液学参数的变化水平,如RBC计数,WBC计数和ESR。关节炎大鼠中促炎性细胞因子(如IL-1β,TNFα和IL-6)的浓度显着较高,但用海藻酸治疗后可降低。通过藻酸治疗显着降低了关节炎期间表现出全身性损伤的溶酶体酶的活性增加,这表明结缔组织破裂和降解的减少。膝关节组织的组织病理学研究表明,广泛的骨降解和滑膜增生以及浸润细胞和藻酸治疗可以逆转组织病理学变化,表明藻酸在类风湿性关节炎中具有保护作用。

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