绿茶中的儿茶素抑制牛和人软骨蛋白多糖和II型胶原的体外降解。

C. Adcocks, P. Collin, D. Buttle
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引用次数: 120

摘要

绿茶中的多酚类化合物已被证明可以减少炎症性关节炎小鼠模型的炎症,但尚未开展研究来调查这些化合物是否对关节组织有保护作用。因此,我们使用体外模型系统研究了绿茶中发现的儿茶素对软骨细胞外基质成分的影响。牛鼻软骨和掌指骨软骨以及人类未患病软骨、骨关节炎和类风湿软骨在有或没有已知的加速软骨基质分解的试剂的情况下进行了培养。在培养物中加入单独的儿茶素,分别用色差法和抑制酶联免疫吸附法测定蛋白聚糖和II型胶原蛋白的释放量。通过乳酸分泌量和蛋白多糖合成来评估儿茶素可能的非特异性或毒性作用。儿茶素,特别是那些含有没食子酸酯的儿茶素,在微摩尔浓度下对抑制蛋白多糖和II型胶原蛋白的分解是有效的。儿茶素没有明显的毒性作用。我们的结论是一些绿茶儿茶素具有软骨保护作用,饮用绿茶可以预防关节炎,并可能通过减少炎症和减缓软骨破坏对关节炎患者有益。需要进一步的研究来确定这些化合物是否以足够的浓度和能够在体内提供功效的形式进入关节空间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catechins from green tea (Camellia sinensis) inhibit bovine and human cartilage proteoglycan and type II collagen degradation in vitro.
Polyphenolic compounds from green tea have been shown to reduce inflammation in a murine model of inflammatory arthritis, but no studies have been undertaken to investigate whether these compounds are protective to joint tissues. We therefore investigated the effects of catechins found in green tea on cartilage extracellular matrix components using in vitro model systems. Bovine nasal and metacarpophalangeal cartilage as well as human nondiseased, osteoarthritic and rheumatoid cartilage were cultured with and without reagents known to accelerate cartilage matrix breakdown. Individual catechins were added to the cultures and the amount of released proteoglycan and type II collagen was measured by metachromatic assay and inhibition ELISA, respectively. Possible nonspecific or toxic effects of the catechins were assessed by lactate output and proteoglycan synthesis. Catechins, particularly those containing a gallate ester, were effective at micromolar concentrations at inhibiting proteoglycan and type II collagen breakdown. No toxic effects of the catechins were evident. We conclude that some green tea catechins are chondroprotective and that consumption of green tea may be prophylactic for arthritis and may benefit the arthritis patient by reducing inflammation and slowing cartilage breakdown. Further studies will be required to determine whether these compounds access the joint space in sufficient concentration and in a form capable of providing efficacy in vivo.
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