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Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model
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 H...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Physiological Society and The Korean Society of Pharmacology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840075/ https://www.ncbi.nlm.nih.gov/pubmed/29520169 http://dx.doi.org/10.4196/kjpp.2018.22.2.163 |
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author | 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 |
author_facet | 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 |
author_sort | Ra, Ho Jong |
collection | PubMed |
description | 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 H(2)O(2) 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. |
format | Online Article Text |
id | pubmed-5840075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Physiological Society and The Korean Society of Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-58400752018-03-08 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 Korean J Physiol Pharmacol Original Article 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 H(2)O(2) 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. The Korean Physiological Society and The Korean Society of Pharmacology 2018-03 2018-02-23 /pmc/articles/PMC5840075/ /pubmed/29520169 http://dx.doi.org/10.4196/kjpp.2018.22.2.163 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article 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 Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
title | Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
title_full | Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
title_fullStr | Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
title_full_unstemmed | Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
title_short | Effects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
title_sort | effects of salmon dna fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840075/ https://www.ncbi.nlm.nih.gov/pubmed/29520169 http://dx.doi.org/10.4196/kjpp.2018.22.2.163 |
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