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International Journal of Pharmaceutical Sciences Research Volume 3 (2016), Article ID 3:IJPSR-115, 6 pages
http://dx.doi.org/10.15344/2394-1502/2016/115
Research Article
Suppressive Activity of Chondroitin Sulfate on Periostin Production by Synoviocytes from Knee Osteoarthritis In Vitro

Daisuke Tamaki1, Shintaro Ishikawa2, Asako Yamada3, Amane Otaki1, and Kazuhito Asano4*

1Graduate School of Health Sciences, Showa University Graduate School, Yokohama, Japan
2Department of Physiology, School of Medicine, Showa University, Tokyo, Japan
3Division of Nursing, Showa University Fujigaoka Hospital, Showa University, Yokohama, Japan
4Division of Physiology, School of Nursing and Rehabilitation Sciences, Showa University, Yokohama, Japan
Prof. Kazuhito Asano, Division of Physiology, School of Nursing and Rehabilitation Sciences, Showa University, 1865 Touka-Ichiba, Midori-Ku, Yokohama 226-8555, Japan; E-mail: asanok@med.showa-u.ac.jp
01 August 2016; 18 October 2016; 20 October 2016
Tamaki D, Ishikawa S, Yamada A, Otaki A, Asano K (2016) Suppressive Activity of Chondroitin Sulfate on Periostin Production by Synoviocytes from Knee Osteoarthritis In Vitro. Int J Pharma Sci Res 3: 115. doi: https://doi.org/10.15344/2394-1502/2016/115

Abstract

Background: Knee osteoarthritis (OA) is well known to be one of the most common joint disease in elderly people and characterized by pain, stiffness and loss of function in articulating joints, which develop slowly and worsen over time. Chondroitin sulfate (CS) and glucosamine hydrochloride are used for the treatment of OA and reported that these substances are favorably modify the clinical symptoms, especially pain, however, the therapeutic mechanisms of these substances are not fully understood. The present study was undertaken to examine the influence of CS on the production of periostin, which is one of the important molecules associated with OA development, by synoviocytes from an OA patient by an in vitro cell culture technique.
Methods: Synoviocytes (1 x 105 cell/ml) were stimulated with 10.0 ng/ml IL-13 in the presence of various concentrations of CS. After 48 h, periostin content in culture supernatants was examined by ELISA. We also examined the influence of CS on transcription factor, STAT6, activation and periostin mRNA expression in synoviocytes 12 and 24 h after IL-13 stimulation, respectively.
Results: Addition of CS into cell cultures caused the suppression of periostin production from synoviocytes induced by IL-13 stimulation through the inhibition of STAT6 activation and periostin mRNA expression. The minimum concentration of CS that caused significant suppression of periostin production, STAT6 activation and mRNA expression was 10.0 μg/ml.
Conclusion: These results strongly suggest that the ability of CS to suppress periostin production from synoviocytes may account, at least in part, for the clinical efficacy of CS on OA.