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Intra-articular injection of modified citrus pectin and hyaluronate gel induces synergistic effects in treating osteoarthritis. | LitMetric

Intra-articular injection of modified citrus pectin and hyaluronate gel induces synergistic effects in treating osteoarthritis.

Int J Biol Macromol

The Key Laboratory of Biomedical Material of Tianjin, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Biomedical Engineering, Tianjin, 300192, PR, China. Electronic address:

Published: September 2024

AI Article Synopsis

  • Modified citrus pectin (MCP) is effective in reducing inflammation and protecting cartilage in osteoarthritis (OA) by inhibiting the pro-inflammatory factor Galectin-3 (Gal-3).
  • A new hyaluronate (HA) gel-based sustained release system (MCP-HA) was tested on OA rabbit models, showing improvements in symptoms, reduction of cartilage degeneration, and suppression of synovial inflammation.
  • Proteomic analysis indicated that MCP-HA not only modulated inflammation but also influenced metabolic pathways, suggesting its potential for long-term treatment of OA.

Article Abstract

We previously found that modified citrus pectin (MCP), an inhibitor of pro-inflammatory factor Galectin-3 (Gal-3), has significant anti-inflammatory and chondroprotective effects. In this study, a hyaluronate (HA) gel-based sustained release system of MCP (MCP-HA) was developed as an anti-inflammatory agent for chronic inflammation for osteoarthritis (OA) treatment. The MCP-HA gel was injected into the knee joint cavities of OA rabbit models induced by anterior cruciate ligament transection (ACLT) or modified Hulth method once a week for five weeks. We found that MCP-HA could improve the symptoms and signs of OA, protect articular cartilage from degeneration, suppress synovial inflammation, and therefore alleviate OA progression. Proteomic analysis of the synovial fluid obtained from the knee joints of OA rabbits revealed that MCP-HA synergistically regulated the levels of multiple inflammatory mediators and proteins involved in metabolic pathways. Taken together, our results demonstrate that the MCP-HA shows a synergistic effect of HA and MCP by modulating both inflammation and metabolic processes, thereby alleviating OA progression. The MCP-HA sustained release system has promising potential for long-term use in OA treatment.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2024.133840DOI Listing

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