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Effect of Different Molecular Weight Hyaluronans on Osteoarthritis-Related Protein Production in Fibroblast-Like Synoviocytes From Patients With Tibia Plateau Fracture

骨关节炎 促炎细胞因子 成纤维细胞 肿瘤坏死因子α 医学 基质金属蛋白酶 白细胞介素 内科学 炎症 化学 内分泌学 癌症研究 病理 生物化学 细胞因子 体外 替代医学
作者
Teng-Le Huang,Horng-Chaung Hsu,Kai‐Chiang Yang,Chun‐Hsu Yao,Feng‐Huei Lin
出处
期刊:Journal of Trauma-injury Infection and Critical Care [Ovid Technologies (Wolters Kluwer)]
卷期号:68 (1): 146-152 被引量:24
标识
DOI:10.1097/ta.0b013e3181a92cf8
摘要

Background: Preventing arthritic change in a joint with an intra-articular fracture remains a challenge, especially in weight-bearing joints. Hyaluronan (HA) has been proven to be effective in relieving joint pain and improving function in chronic osteoarthritis. However, controversy still exists about its potential use in a joint with an intra-articular fracture and about whether this effect is dependent on molecular weight. We analyzed and compared the effects of two different molecular weight HAs on six osteoarthritis-related proteins expressed in fibroblast-like synoviocytes from 12 patients with tibial plateau fracture. Methods: The interleukin (IL)-1β–stimulated or IL-1β–unstimulated fibroblast-like synoviocytes were cultivated with or without treatment by two different molecular weight HAs. The production of these proteins was quantified by using commercially available sandwich enzyme-linked immunosorbent assay. Results: The results revealed that HA with a high molecular weight is more effective in downregulating proinflammatory cytokines such as interleukin-1β and tumor necrosis factor-α. Conversely, HA with a low molecular weight has greater efficacy in upregulating anticatabolic enzymes, such as tissue inhibitor of metalloproteinase-1 and tissue inhibitor of metalloproteinase-2, and in suppressing the catabolic enzyme, matrix metalloproteinase-3, which are thought to be more chondroprotective. Conclusions: In a knee joint with an intra-articular fracture of the tibial plateau, we posit that high molecular weight HA may have a better anti-inflammatory effect, whereas low molecular weight HA has superior efficacy for chondroprotection.
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