Your browser doesn't support javascript.
loading
Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model.
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.
Afiliação
  • Ra HJ; Department of Orthopedic Surgery, Gangneung Asan Hospital, Ulsan University College of Medicine, Gangneung 25440, Korea.
  • Oh MY; Medical Research Institute, Gangneung Asan Hospital, Gangneung 25440, Korea.
  • Kim HJ; Medical Research Institute, Gangneung Asan Hospital, Gangneung 25440, Korea.
  • Lee SY; Medical Research Institute, Gangneung Asan Hospital, Gangneung 25440, Korea.
  • Eom DW; Department of Pathology, Gangneung Asan Hospital, Ulsan University College of Medicine, Gangneung 25440, Korea.
  • Lee SK; Department of Orthopedic Surgery, Gangneung Asan Hospital, Ulsan University College of Medicine, Gangneung 25440, Korea.
  • Kim SN; Natural Products Research Institute, Korea Institute of Science and Technology, Gangneung 25440, Korea.
  • Chung KS; Department of Orthopedic Surgery, Hanil General Hospital, Seoul 01450, Korea.
  • Jang HJ; Department of Surgery, Gangneung Asan Hospital, Ulsan University College of Medicine, Gangneung 25440, Korea.
Korean J Physiol Pharmacol ; 22(2): 163-172, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29520169
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 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-1ß, TNF-α, COX-2, iNOS, and PGE2, were significantly suppressed by PRF001 treatment. In vivo, the inflammatory mediators and cytokines, IL-1ß, 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-1ß, TNF-α, and subsequent signals, such as p-Erk1/2, NF-κB, COX-2, PGE2, and MMPs.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Korean J Physiol Pharmacol Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Korean J Physiol Pharmacol Ano de publicação: 2018 Tipo de documento: Article