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A pharmacoproteomic study confirms the synergistic effect of chondroitin sulfate and glucosamine

机译:药理学研究证实了硫酸软骨素和氨基葡萄糖的协同作用

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摘要

Osteoarthritis (OA) is the most common age-related rheumatic disease. Chondrocytes play a primary role in mediating cartilage destruction and extracellular matrix (ECM) breakdown, which are main features of the OA joint. Quantitative proteomics technologies are demonstrating a very interesting power for studying the molecular effects of some drugs currently used to treat OA patients, such as chondroitin sulfate (CS) and glucosamine (GlcN). In this work, we employed the iTRAQ (isobaric tags for relative and absolute quantitation) technique to assess the effect of CS and GlcN, both alone and in combination, in modifying cartilage ECM metabolism by the analysis of OA chondrocytes secretome. 186 different proteins secreted by the treated OA chondrocytes were identified. 36 of them presented statistically significant differences (p ≤ 0.05) between untreated and treated samples: 32 were increased and 4 decreased. The synergistic chondroprotective effect of CS and GlcN, firstly reported by our group at the intracellular level, is now demonstrated also at the extracellular level.
机译:骨关节炎(OA)是最常见的与年龄有关的风湿病。软骨细胞在介导软骨破坏和细胞外基质(ECM)分解中起主要作用,这是OA关节的主要特征。定量蛋白质组学技术在研究目前用于治疗OA患者的某些药物(例如硫酸软骨素(CS)和葡萄糖胺(GlcN))的分子效应方面显示出非常有趣的力量。在这项工作中,我们采用了iTRAQ(相对和绝对定量等压标记)技术,通过分析OA软骨细胞分泌组,评估了CS和GlcN单独或组合使用在修饰软骨ECM代谢中的作用。鉴定出由经处理的OA软骨细胞分泌的186种不同蛋白质。其中有36个在未经处理的样本和经处理的样本之间具有统计学差异(p≤0.05):增加了32个,减少了4个。我们小组在细胞内水平上首次报道了CS和GlcN的协同软骨保护作用,现在也在细胞外水平上证明了这一点。

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