Cyclooxygenase expression in synovial tissue of patients with rheumatoid arthritis and rats with experimental arthritis.
Hajime Sano, Motoharu Kondo, Ronald L. Wilder
Abstract
Open-access reader
Hajime Sano, Motoharu Kondo, Ronald L. Wilder
Abstract
Open-access reader
Cyclooxygenase (COX) plays a role in inflammatory diseases, but limited data exist on the regulation of COXin vivo. We studied thein vivoexpression of COX in synovia from patients with rheumatoid arthritis (RA) as well as rats with streptococcal cell wall (SCW) and adjuvant arthritis. Extensive and intense COX immunostaining, which correlated with the intensity of mononuclear cell infiltration, was observed in RA synovia. Significantly less staining was noted in OA and normal human synovia. COX immunostaining was equivocal in the joints of normal and arthritis-resistant F344/N rats. In contrast, high level COX expression developed rapidly in female LEW/N rats throughout hindlimb joints preceeding or paralleling experimental arthritis.COX was expressed in the joints of athymic LEW. rnu/rnu rats 2-4 days after injection of SCW or adjuvant but was not sustained. Physiological doses of glucocorticoids suppressed both arthritis and COX expression in LEW/N rats injected with SCW or adjuvant.These observations suggest that, in vivo, (a) COX expression is upregulated in inflammatory joint diseases, (b) expression is a biochemical marker of disease activity, and (c) expression is down-regulated by antiinflammatory glucocorticoids.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Cyclooxygenase (COX) plays a role in inflammatory diseases, but limited data exist on the regulation of COXin vivo. We studied thein vivoexpression of COX in synovia from patients with rheumatoid arthritis (RA) as well as rats with streptococcal cell wall (SCW) and adjuvant arthritis. Extensive and intense COX immunostaining, which correlated with the intensity of mononuclear cell infiltration, was observed in RA synovia. Significantly less staining was noted in OA and normal human synovia. COX immunostaining was equivocal in the joints of normal and arthritis-resistant F344/N rats. In contrast, high level COX expression developed rapidly in female LEW/N rats throughout hindlimb joints preceeding or paralleling experimental arthritis.COX was expressed in the joints of athymic LEW. rnu/rnu rats 2-4 days after injection of SCW or adjuvant but was not sustained. Physiological doses of glucocorticoids suppressed both arthritis and COX expression in LEW/N rats injected with SCW or adjuvant.These observations suggest that, in vivo, (a) COX expression is upregulated in inflammatory joint diseases, (b) expression is a biochemical marker of disease activity, and (c) expression is down-regulated by antiinflammatory glucocorticoids.
Key concepts: Rheumatoid arthritis, Immunostaining, Arthritis, Medicine, Cyclooxygenase, In vivo, Pathology, Inflammation