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Effects of gangliosides from deer bone extract on the gene expressions of matrix metalloproteinases and collagen type II in interleukin-1 beta-induced osteoarthritic chondrocytes

Authors
Suh, Hyung JooLee, HyunjiMin, Byung JungJung, Sung UgJung, Eun Young
Issue Date
Dec-2016
Publisher
KOREAN NUTRITION SOC
Keywords
Chondrocytes; collagen type II; interleukin-1 beta; matrix metalloproteinases; osteoarthritis
Citation
NUTRITION RESEARCH AND PRACTICE, v.10, no.6, pp.569 - 574
Indexed
SCIE
SCOPUS
KCI
Journal Title
NUTRITION RESEARCH AND PRACTICE
Volume
10
Number
6
Start Page
569
End Page
574
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/86617
DOI
10.4162/nrp.2016.10.6.569
ISSN
1976-1457
Abstract
BACKGROUND/OBJECTIVES: We investigated the anti-osteoarthritic effects of deer bone extract on the gene expressions of matrix metalloproteinases (MMPs) and collagen type II (COL2) in interleukin-1 beta-induced osteoarthritis (OA) chondrocytes. MATERIALS/METHODS: Primary rabbit chondrocytes were treated as follows: CON (PBS treatment), NC (IL-1 beta treatment), PC (IL-1 beta + 100 mu g/mL glucosamine sulphate/chondroitin sulphate mixture), and DB (IL-1 beta + 100 mu g/mL. deer bone extract). RESULTS: The results of the cell viability assay indicated that deer bone extract at doses ranging from 100 to 500 mu g/mL inhibits cell death in chondrocytes induced by IL-1 beta. Deer bone extract was able to significantly recover the mRNA expression of COL2 that was down-regulated by IL-1 beta (NC: 0.79 vs. DB: 0.87, P < 0.05) and significantly decrease the mRNA expression of MMP-3 (NC: 2.24 vs. DB: 1.75) and -13 (NC: 1.28 vs. DB: 0.89) in OA chondrocytes (P < 0.05). CONCLUSIONS: We concluded that deer bone extract induces accumulation of COL2 through the down-regulation of MMPs in IL-1 beta-induced OA chondrocytes. Our results suggest that deer bone extract, which contains various components related to OA, including chondroitin sulphate, may possess anti-osteoarthritic properties and be of value in inhibiting the pathogenesis of OA.
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