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Cellular pharmacodynamic effects of Pycnogenol? in patients with severe osteoarthritis: a randomized controlled pilot study

机译:碧萝ogen的细胞药效作用?重度骨关节炎患者:一项随机对照试验研究

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The standardized maritime pine bark extract (Pycnogenol?) has previously shown symptom alleviating effects in patients suffering from moderate forms of knee osteoarthritis (OA). The cellular mechanisms for this positive impact are so far unknown. The purpose of the present randomized pilot controlled study was to span the knowledge gap between the reported clinical effects of Pycnogenol? and its in vivo mechanism of action in OA patients. Thirty three patients with severe OA scheduled for a knee arthroplasty either received 100?mg of Pycnogenol? twice daily or no treatment (control group) three weeks before surgery. Cartilage, synovial fluid and serum samples were collected during surgical intervention. Relative gene expression of cartilage homeostasis markers were analyzed in the patients’ chondrocytes. Inflammatory and cartilage metabolism mediators were investigated in serum and synovial fluid samples. The oral intake of Pycnogenol? downregulated the gene expression of various cartilage degradation markers in the patients’ chondrocytes, the decrease of MMP3, MMP13 and the pro-inflammatory cytokine IL1B were statistically significant (p?≤?0.05). Additionally, protein concentrations of ADAMTS-5 in serum were reduced significantly (p?≤?0.05) after three weeks intake of the pine bark extract. This is the first report about positive cellular effects of a dietary supplement on key catabolic and inflammatory markers in patients with severe OA. The results provide a rational basis for understanding previously reported clinical effects of Pycnogenol? on symptom scores of patients suffering from OA. ISRCTN10754119 . Retrospectively registered 08/10/2015.
机译:标准化的海上松树皮提取物(碧萝ogen)以前已显示出对患有中度形式的膝骨关节炎(OA)的患者的症状缓解作用。迄今为止尚不清楚这种积极影响的细胞机制。本随机先导对照研究的目的是消除碧萝ogen的已报道临床疗效之间的知识差距。及其在OA患者体内的作用机理。预定进行膝关节置换术的33例严重OA的患者接受了100mg碧容健?手术前三周每天两次或不治疗(对照组)。在外科手术期间收集软骨,滑液和血清样品。分析了患者软骨细胞中软骨稳态标记物的相对基因表达。在血清和滑液样本中研究了炎症和软骨代谢介质。碧萝ogen的口服摄入量?下调患者软骨细胞中各种软骨降解标志物的基因表达,MMP3,MMP13和促炎细胞因子IL1B的降低具有统计学意义(p≤≤0.05)。另外,摄入松树皮提取物三周后,血清中ADAMTS-5的蛋白质​​浓度显着降低(p≤≤0.05)。这是有关膳食补充剂对重症OA患者关键代谢和炎性标志物的积极细胞作用的首次报道。该结果为理解碧萝ogen的先前报道的临床疗效提供了合理的基础。对OA患者的症状评分。 ISRCTN10754119。追溯注册于2015年8月10日。

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