首页> 外文期刊>The Veterinary Journal >Evaluation of intra-articular hyaluronan, sodium chondroitin sulfate and N-acetyl-D-glucosamine combination versus saline (0.9% NaCl) for osteoarthritis using an equine model
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Evaluation of intra-articular hyaluronan, sodium chondroitin sulfate and N-acetyl-D-glucosamine combination versus saline (0.9% NaCl) for osteoarthritis using an equine model

机译:使用马模型评估关节内透明质酸,硫酸软骨素钠和N-乙酰基-D-葡萄糖胺联合盐水(0.9%NaCl)对骨关节炎的评估

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摘要

A randomized blinded placebo controlled trial was conducted to assess the clinical, biochemical and histological effects of a hyaluronan, sodium chondroitin sulfate and N-acetyl-D-glucosamine combination (PG) administered through an intra-articular (IA) route for the treatment of osteoarthritis (OA) at the time of injury. OA was induced in one carpal joint of each of 16 horses. Horses were designated placebo or IA PG treated. All horses were treated with 125 mg amikacin sulfate IA and 5 mL physiological saline in the middle carpal joint bilaterally on study Days 0 (after induction of OA), 7, 14 and 28, except the OA affected joint of the IA PG horses, which received 5 mL PG plus 125 mg of amikacin sulfate on similar days. Evaluations included clinical and radiographic, synovial fluid analysis, gross and histological examinations, as well as histochemical and biochemical analyses. The model induced a significant pathology that resulted in clinical disease. No adverse treatment-related events were detected in any of the horses. Intra-articular treatment of OA-affected joints with PG resulted in a transient 16% improvement in clinical pain (lameness scores) and evidence of improvement trends in bone proliferation radiographically as well as in the degree of full thickness articular cartilage erosion seen grossly when compared to placebo treated OA affected joints, although the vast majority of outcome parameters were not significantly different than controls. The findings support some potential clinical sign or disease modifying action of this compound administered IA at the tested dose and frequency
机译:进行了一项随机双盲安慰剂对照试验,以评估通过关节内(IA)途径给药的透明质酸,硫酸软骨素钠和N-乙酰基-D-葡萄糖胺联合(PG)的临床,生化和组织学作用。受伤时的骨关节炎(OA)。在每16匹马的一个腕关节中诱发OA。将马指定为安慰剂或IA PG治疗。在研究的第0天(诱导OA后),第7、14和28天,所有马均在双腕腕中部接受125 mg硫酸丁胺卡那霉素IA和5 mL生理盐水治疗,除了IA PG马受OA影响的关节外。在相似的日期接受了5 mL PG和125 mg硫酸丁胺卡那霉素。评估包括临床和影像学,滑液分析,肉眼和组织学检查,以及组织化学和生化分析。该模型诱发了导致临床疾病的重大病理。在任何一匹马中均未发现与治疗相关的不良事件。与PG进行关节腔内治疗OA受影响的关节后,临床疼痛(lameness评分)得到了短暂的16%改善,并且影像学显示骨增生以及全层关节软骨侵蚀程度明显改善时,骨增生的改善趋势得到了证明尽管绝大多数结果参数与对照组无显着差异,但安慰剂治疗的OA受影响的关节仍未见明显改变。这些发现支持了以测试剂量和频率进行IA给药的该化合物的某些潜在临床症状或疾病改变作用

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