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      The role of peroxynitrite in cyclooxygenase-2 expression of rheumatoid synovium.

      Clinical and experimental rheumatology
      Arthritis, Rheumatoid, metabolism, Cells, Cultured, Gene Expression Regulation, Enzymologic, drug effects, physiology, Humans, Molsidomine, analogs & derivatives, pharmacology, Nitric Oxide, Nitric Oxide Donors, Peroxynitrous Acid, Prostaglandin-Endoperoxide Synthases, genetics, RNA, Messenger, analysis, Synovial Membrane, cytology, enzymology

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          Abstract

          Reactive oxygen intermediates play an important role in the inflammatory processes of rheumatoid arthritis. Cyclooxygenase-2 is an inducible form of an enzyme involved in prostanoid biosynthesis. This study linked peroxynitrite (ONOO-) to the signaling pathways that induce COX-2. Exposure of rheumatoid synovial cells to peroxynitrite resulted in COX-2 protein expression in a dose-dependent manner. RT-PCR analysis also demonstrated that COX-2 mRNA was induced in peroxynitrite-treated rheumatoid synovial cells. Dexamethasone markedly inhibited this peroxynitrite-mediated COX-2 expression at therapeutic concentrations. This study demonstrates that oxidant stress is an important inducer of COX-2 in rheumatoid synovium. This induction may contribute to the amplification of prostanoids in the rheumatoid inflammatory process.

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