马钱苷调控巨噬细胞极化对骨关节炎进展的作用机制

    Study on the mechanism of loganin regulating macrophage polarization on the progression of osteoarthritis

    • 摘要:
      目的: 探究马钱苷调控巨噬细胞极化对骨关节炎(OA)进展的的影响及可能作用机制。
      方法: 将30只大鼠分为假手术组、OA组及马钱苷 + OA组,每组10只。micro-CT检测膝关节骨密度(BMD)及骨矿物质含量(BMC)。番红O染色软骨与滑膜组织病理损伤并进行OARSI评分。免疫荧光染色检测滑膜组织CD86及CD163表达水平。免疫组织化学染色检测软骨与滑膜组织TNF-α蛋白表达水平。Western blot检测IL-6及IL-1β蛋白表达水平。
      结果: 与假手术组相比,OA组大鼠膝关节骨质疏松,BMD与BMC减少(P < 0.05),膝关节软骨损伤变薄,表面裂隙增加,软骨细胞排列整齐,OARSI评分增加(P < 0.05),滑膜组织M1型巨噬细胞标记蛋白CD86与M2型巨噬细胞标记蛋白CD163表达增加,软骨与滑膜组织TNF-α、IL-6及IL-1β蛋白表达增加(P < 0.05);与OA组相比,马钱苷 + OA组大鼠膝关节骨质疏松改善,BMD与BMC减少(P < 0.05),膝关节软骨损伤改善,软骨细胞排列较整齐,OARSI评分减少(P < 0.05),滑膜组织CD86表达减少,CD163表达增加,软骨与滑膜组织TNF-α、IL-6及IL-1β蛋白表达减少(P < 0.05)。
      结论: 马钱苷可通过促进M2型巨噬细胞极化改善OA大鼠膝关节损伤。

       

      Abstract:
      Objective To investigate the effects of loganin regulating macrophage polarization on the progression of osteoarthritis (OA) and its possible mechanism.
      Methods Thirty rats were randomly divided into the sham operation group, OA group and loganin + OA group, with 10 rats in each group. The bone mineral density (BMD) and bone mineral content (BMC) were measured by micro-CT. The pathological damage of cartilage and synovial tissue were stained with Safranin O, and scored by OARSI. Immunofluorescence staining was used to detect the expression of CD86 and CD163 in synovial tissue. The expression levels of TNF-α protein in cartilage and synovial tissue were detected using immunohistochemical staining. The protein expression levels of IL-6 and IL-1β were detected by Western blot.
      Results Compared with the sham-operated group, the osteoporosis in the knee joint was found, BMD and BMC decreased (P < 0.05), the knee cartilage damage thinned, the knee surface fissure increased, the chondrocytes neatly arranged, the OARSI score increased (P < 0.05). the expression levels of M1 macrophage marker protein CD86 and M2 macrophage marker protein CD163 in the synovial tissue increased, and the expression levels of TNF-α, IL-6, and IL-1β in the cartilage and synovial tissue increased (P < 0.05). Compared with the OA group, the osteoporosis in the knee joint was improved, the BMD and BMC decreased (P < 0.05), the knee cartilage injury was improved, the chondrocytes were arranged more neatly, the OARSI score decreased (P < 0.05), the CD86 expression in synovial tissue decreased, the CD163 expression increased, and the protein expression levels of TNF-α, IL-6 and IL-1β in cartilage and synovial tissues decreased in the logain + OA group (P < 0.05).
      Conclusions Loganin can improve knee joint injury in OA rats by promoting M2 macrophage polarization.

       

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