首页> 美国卫生研究院文献>Annals of the Rheumatic Diseases >Effects of tiaprofenic acid (Surgam) on cartilage proteoglycans in the rabbit joint immobilisation model.
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Effects of tiaprofenic acid (Surgam) on cartilage proteoglycans in the rabbit joint immobilisation model.

机译:噻洛芬酸(Surgam)对家兔关节固定模型中软骨蛋白聚糖的影响。

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摘要

A well established model of arthritis induced in rabbit knee joints by immobilisation in full extension for 30 days was used to evaluate the in vivo effects of 2.5, 5.0, and 10.0 mg/kg body weight of tiaprofenic acid on articular cartilage proteoglycans. The drug was given subcutaneously every 24 hours during the entire immobilisation period. Immobilised animals not treated with drugs and normal animals were used as controls. In the non-drug treated immobilised animals articular cartilage showed evidence of surface damage accompanied by synovial hypertrophy and effusion. Proteoglycan concentrations were reduced in cartilages of these joints and the incorporation of 35SO2-4 into macromolecular proteoglycans was higher than in cartilages of non-immobilised controls. Gel filtration chromatographic studies of both resident and 35S labelled proteoglycans isolated from immobilised joint cartilage showed reduced aggregation and the presence of degraded proteoglycan subunit species. Whereas the administration of 10.0 mg/kg tiaprofenic acid every 24 hours to immobilised animals exacerbated the degradation and loss of proteoglycans from joint cartilages, 5.0 mg/kg tiaprofenic acid provided some protection of these macromolecules, as shown by the concentrations and extractability of proteoglycans from cartilages, which were comparable with those from non-immobilised controls. A high incorporation of 35S into proteoglycans was demonstrated, together with reduced catabolism of proteoglycans, indicating preservation of chondrocyte anabolic activity. At a tiaprofenic acid dose of 2.5 mg/kg, however, no beneficial effects on cartilage proteoglycans could be shown.
机译:通过完全固定固定30天在兔膝关节中诱发的关节炎建立的良好模型用于评估2.5、5.0和10.0 mg / kg体重的噻洛芬酸对关节软骨蛋白聚糖的体内作用。在整个固定期间,每24小时皮下注射一次药物。未用药物治疗的固定化动物和正常动物用作对照。在未经药物治疗的固定化动物中,关节软骨显示出表面损伤的迹象,伴有滑膜肥大和积液。这些关节软骨中的蛋白聚糖浓度降低,并且将35SO2-4掺入大分子蛋白聚糖中的比例高于未固定对照的软骨中。从固定的关节软骨中分离出的常驻蛋白和35S标记蛋白聚糖的凝胶过滤色谱研究表明,聚集减少,蛋白聚糖亚基降解。每24小时给固定的动物施用10.0 mg / kg的噻洛芬酸会加剧关节软骨中蛋白聚糖的降解和损失,而5.0 mg / kg的噻洛芬酸对这些大分子提供了一定的保护作用,如蛋白聚糖的浓度和可提取性所示。软骨,与非固定对照的软骨相当。证明了将35S高度掺入蛋白聚糖,以及蛋白聚糖的分解代谢降低,表明软骨细胞合成代谢活性得以保持。然而,在噻洛芬酸剂量为2.5 mg / kg时,未显示出对软骨蛋白聚糖的有益作用。

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