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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2018
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.
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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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