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首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model
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Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model

机译:鲑鱼DNA组分在碘乙酸单钠诱导的骨关节炎大鼠模型中的作用

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PRF001 is a fragmented DNA polymer extracted from the testes of salmon. The purpose of this study was to assess the anti-inflammatory effect of PRF001 in vitro as well as the protective effect of PRF001 intake against arthritis in a rat model. In vitro , cell survival and inflammatory markers after H2O2 treatment to induce cell damage were investigated in CHON-001 cells treated with different concentrations of PRF001. In vivo , osteoarthritis was induced by intra-articular injection of monosodium iodoacetate (MIA) into the knee joints of rats. After consumption of PRF001 (10, 50, or 100 mg/kg) for 4 weeks, inflammatory mediators and cytokines in articular cartilage were investigated. In vitro, the levels of inflammatory markers, IL-1β, TNF-α, COX-2, iNOS, and PGE2, were significantly suppressed by PRF001 treatment. In vivo , the inflammatory mediators and cytokines, IL-1β, p-Erk1/2, NF-κB, TNF-α, COX-2, and PGE2, as well as MMP3 and MMP7, which have catabolic activity in chondrocytes, were decreased in the MIA-induced osteoarthritic rats following intake of PRF001. Histological analysis revealed that PRF001 had a protective effect on the articular cartilage. Altogether, these results demonstrated that the anti-inflammatory property of PRF001 contributes to its protective effects in osteoarthritis through deregulating IL-1β, TNF-α, and subsequent signals, such as p-Erk1/2, NF-κB, COX-2, PGE2, and MMPs.
机译:PRF001是从鲑鱼睾丸中提取的片段DNA聚合物。这项研究的目的是评估大鼠模型中PRF001的体外抗炎作用以及PRF001摄入量对关节炎的保护作用。在体外,研究了在不同浓度的PRF001处理的CHON-001细胞中,H 2 O 2 处理后诱导细胞损伤的细胞存活和炎症标志物。在体内,通过将碘乙酸单钠(MIA)关节内注射到大鼠的膝关节中来诱发骨关节炎。服用PRF001(10、50或100 mg / kg)4周后,研究了关节软骨中的炎症介质和细胞因子。在体外,通过PRF001处理可明显抑制炎症标志物IL-1β,TNF-α,COX-2,iNOS和PGE2的水平。在体内,减少了在软骨细胞中具有分解代谢活性的炎症介质和细胞因子,IL-1β,p-Erk1 / 2,NF-κB,TNF-α,COX-2和PGE2以及MMP3和MMP7。摄入PRF001后在MIA诱发的骨关节炎大鼠中的作用。组织学分析表明,PRF001对关节软骨具有保护作用。总而言之,这些结果表明PRF001的抗炎特性通过使IL-1β,TNF-α和随后的信号(例如p-Erk1 / 2,NF-κB,COX-2, PGE2和MMP。

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