alpha-(4-pyridyl-1-oxide)-n-tert-butylnitrone and Osteoarthritis

Chondrocytes have been shown to produce superoxide and hydrogen peroxide, suggesting possible formation of hydroxyl radical in these cells. In this study, we used electron spin resonance/spin trapping technique to detect hydroxyl radicals in chondrocytes. We found that hydroxyl radicals could be detected as alpha-hydroxyethyl spin trapped adduct of 4-pyridyl 1-oxide N-tert-butylnitrone (4-POBN) in chondrocytes stimulated with phorbol 12-myristate 13-acetate in the presence of ferrous ion. The formation of hydroxyl radical appears to be mediated by the transition metal-catalyzed Haber-Weiss reaction since no hydroxyl radical was detected in the absence of exogenous iron. The hydroxyl radical formation was inhibited by catalase but not by superoxide dismutase, suggesting that the hydrogen peroxide is the precursor. Cytokines, IL-1 and TNF enhanced the hydroxyl radical formation in phorbol 12-myristate 13-acetate treated chondrocytes. Interestingly, hydroxyl radical could be detected in unstimulated fresh human and rabbit cartilage tissue pieces in the presence of iron. These results suggest that the formation of hydroxyl radical in cartilage could play a role in cartilage matrix degradation.

Topics: Animals; Cartilage; Chondrocytes; Electron Spin Resonance Spectroscopy; Ethanol; Female; Humans; Hydroxyl Radical; Interleukin-1; Male; Nitrogen Oxides; Osteoarthritis; Pyridines; Rabbits; Spin Labels; Spin Trapping; Synovial Fluid; Tetradecanoylphorbol Acetate; Tumor Necrosis Factor-alpha