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鲑鱼DNA组分在碘乙酸钠诱导的骨关节炎大鼠模型中的作用。

Effects of salmon DNA fraction and in a monosodium iodoacetate-induced osteoarthritis rat model.

作者信息

Ra Ho Jong, Oh Mi Young, Kim Hee Ju, Lee Seung Yong, Eom Dae Woon, Lee Suk Kyu, Kim Su-Nam, Chung Kyu Sung, Jang Hyuk Jai

机构信息

Department of Orthopedic Surgery, Gangneung Asan Hospital, Ulsan University College of Medicine, Gangneung 25440, Korea.

Medical Research Institute, Gangneung Asan Hospital, Gangneung 25440, Korea.

出版信息

Korean J Physiol Pharmacol. 2018 Mar;22(2):163-172. doi: 10.4196/kjpp.2018.22.2.163. Epub 2018 Feb 23.

DOI:10.4196/kjpp.2018.22.2.163
PMID:29520169
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5840075/
Abstract

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 as well as the protective effect of PRF001 intake against arthritis in a rat model. , cell survival and inflammatory markers after HO treatment to induce cell damage were investigated in CHON-001 cells treated with different concentrations of PRF001. , 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. , 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.

摘要

PRF001是一种从鲑鱼睾丸中提取的片段化DNA聚合物。本研究的目的是评估PRF001的抗炎作用以及在大鼠模型中摄入PRF001对关节炎的保护作用。在用不同浓度PRF001处理的CHON - 001细胞中,研究了HO处理诱导细胞损伤后的细胞存活和炎症标志物。通过向大鼠膝关节内注射碘乙酸钠(MIA)诱导骨关节炎。在摄入PRF001(10、50或100mg/kg)4周后,研究关节软骨中的炎症介质和细胞因子。在体外,PRF001处理可显著抑制炎症标志物IL - 1β、TNF - α、COX - 2、iNOS和PGE2的水平。在摄入PRF001后,MIA诱导的骨关节炎大鼠中,炎症介质和细胞因子IL - 1β、p - Erk1/2、NF - κB、TNF - α、COX - 2和PGE2以及在软骨细胞中具有分解代谢活性的MMP3和MMP7均减少。组织学分析表明PRF001对关节软骨具有保护作用。总之,这些结果表明PRF001的抗炎特性通过调节IL - 1β、TNF - α以及随后的信号,如p - Erk1/2、NF - κB、COX - 2、PGE2和MMPs,对骨关节炎起到保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/858067a8e64e/kjpp-22-163-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/fa51dfdf6449/kjpp-22-163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/304dbed8f6c0/kjpp-22-163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/8a411479ac0a/kjpp-22-163-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/a845a351ce86/kjpp-22-163-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/858067a8e64e/kjpp-22-163-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/fa51dfdf6449/kjpp-22-163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/304dbed8f6c0/kjpp-22-163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/8a411479ac0a/kjpp-22-163-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/a845a351ce86/kjpp-22-163-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea12/5840075/858067a8e64e/kjpp-22-163-g005.jpg

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