Abstract

Background: Knee osteoarthritis (OA) is well known to be one of the most common joint disease in elderly people and characterized by a slowly progression of articular cartilage thinning and remodeling of the joints. Glucosamine hydrochloride (GH) and chondroitin sulfate, either alone or combined, are used for the treatment of OA and reported that these substances are favorably modify the clinical symptoms, especially pain, however, the underlying therapeutic mechanisms of these substances are not completely clear. The present study was undertaken to examine the influence of GH on the production of nitric oxide (NO), which is one of the important final effector molecules associated with OA, from synoviocytes from OA patients by an in vitro cell culture technique. Methods: Synoviocytes (1x105 cell/ml) were stimulated with 100.0 ng/ml periostin in the presence of various concentrations of GH. After 24 h, NO content in culture supernatants was examined by the Griess method. We also examined the influence of GH on transcription factor, NF-κB, activation and iNOS mRNA expression in synoviocytes 4 and 12 h after periostin stimulation, respectively. Results: Addition of GH into cell cultures caused the suppression of NO production from synoviocytes induced by periostin stimulation through the suppression of NF-κB activation and iNOS mRNA expression. The minimum concentration of GH that caused significant suppression of NO production was 1.5 mg/ml. Conclusion: These results strongly suggest that the ability of GH to suppress NO production from synoviocytes may account, at least in part, for the clinical efficacy of GH on OA.

Highlights

  • Osteoarthritis of the knee (OA) is well known to be a disease characterized by pain, stiffness, swelling and deformation of the joints, which develop slowly and worsen over time [1, 2]

  • We examined the influence of Glucosamine hydrochloride (GH) on transcription factor, NF-κB, activation and inducible NOS (iNOS) mRNA expression in synoviocytes 4 and 12 h after periostin stimulation, respectively

  • The minimum concentration of GH that caused significant suppression of nitric oxide (NO) production was 1.5 mg/ml. These results strongly suggest that the ability of GH to suppress NO production from synoviocytes may account, at least in part, for the clinical efficacy of GH on OA

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Summary

Introduction

Osteoarthritis of the knee (OA) is well known to be a disease characterized by pain, stiffness, swelling and deformation of the joints, which develop slowly and worsen over time [1, 2]. Int J Pharma Sci Res ISSN: 2394-1502 are much evidence that oral administration of dietary supplements, especially glucosamine hydrochloride (GH) and chondroitin sulfate into patients with OA could favorably modify the clinical conditions of the disease such as pain, stiffness and joint swelling [11,12,13,14]. It is reported the suppressive effects of GH and chondroitin sulfate on joint space narrowing and osteoarthritis progression [15]. The present study, was undertaken to examine the influence of GH on periostin-induced biochemical mechanisms responsible for the development of OA through examining the influence of GH on the production of NO, which is an important final effector molecule in the development of OA, from synoviocytes in vitro

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