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The effects of static and intermittent compression on nitric oxide production in articular cartilage explants
Author(s) -
Fermor Beverley,
Weinberg J. Brice,
Pisetsky David S.,
Misukonis Mary A.,
Banes Albert J.,
Guilak Farshid
Publication year - 2001
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1016/s0736-0266(00)00049-8
Subject(s) - nitric oxide , cartilage , in vivo , chemistry , nitric oxide synthase , osteoarthritis , viability assay , downregulation and upregulation , in vitro , compression (physics) , chondrocyte , endocrinology , medicine , andrology , anatomy , pathology , biology , biochemistry , materials science , microbiology and biotechnology , composite material , alternative medicine , gene
Nitric oxide (NO) production and NO synthase (NOS) expression are increased in osteoarthritis and rheumatoid arthritis, suggesting that NO may play a role in the destruction of articular cartilage. To test the hypothesis that mechanical stress may increase NO production by chondrocytes, we measured the effects of physiological levels of static and intermittent compression on NOS activity, NO production, and NOS antigen expression by porcine articular cartilage explants. Static compression significantly increased NO production at 0.1 MPa stress for 24 h ( P < 0.05). Intermittent compression at 0.5 Hz for 6 h followed by 18 h recovery also increased NO production and NOS activity at 1.0 MPa stress ( P < 0.05). Intermittent compression at 0.5 Hz for 24 h at a magnitude of 0.1 or 0.5 MPa caused an increase in NO production and NOS activity ( P < 0.05). Immunoblot analysis showed stress‐induced upregulation of NOS2, but not NOSI or NOS3. There was no loss in cell viability following any of the loading regimens. Addition of 2 mM 1400 W (a specific NOS2 inhibitor) reduced NO production by 51% with no loss of cell viability. These findings indicate that NO production by chondrocytes is influenced by mechanical compression in vitro and suggest that biome‐chanical factors may in part regulate NO production in vivo. © 2001 Orthopaedic Research Society. Published by Elsevier Science Ltd. All rights reserved.