{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T09:52:30Z","timestamp":1791107550255,"version":"4.1.0"},"reference-count":28,"publisher":"American Physiological Society","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Heart and Circulatory Physiology"],"published-print":{"date-parts":[[2003,12]]},"abstract":"<jats:p>Oscillatory shear stress occurs at sites of the circulation that are vulnerable to atherosclerosis. Because oxidative stress contributes to atherosclerosis, we sought to determine whether oscillatory shear stress increases endothelial production of reactive oxygen species and to define the enzymes responsible for this phenomenon. Bovine aortic endothelial cells were exposed to static, laminar (15 dyn\/cm<jats:sup>2<\/jats:sup>), and oscillatory shear stress (\u00b115 dyn\/cm<jats:sup>2<\/jats:sup>). Oscillatory shear increased superoxide ([Formula: see text]) production by more than threefold over static and laminar conditions as detected using electron spin resonance (ESR). This increase in [Formula: see text] was inhibited by oxypurinol and culture of endothelial cells with tungsten but not by inhibitors of other enzymatic sources. Oxypurinol also prevented H<jats:sub>2<\/jats:sub>O<jats:sub>2<\/jats:sub>production in response to oscillatory shear stress as measured by dichlorofluorescin diacetate and Amplex Red fluorescence. Xanthine-dependent [Formula: see text] production was increased in homogenates of endothelial cells exposed to oscillatory shear stress. This was associated with decreased xanthine dehydrogenase (XDH) protein levels and enzymatic activity resulting in an elevated ratio of xanthine oxidase (XO) to XDH. We also studied endothelial cells lacking the p47<jats:sup>phox<\/jats:sup>subunit of the NAD(P)H oxidase. These cells exhibited dramatically depressed [Formula: see text] production and had minimal XO protein and activity. Transfection of these cells with p47<jats:sup>phox<\/jats:sup>restored XO protein levels. Finally, in bovine aortic endothelial cells, prolonged inhibition of the NAD(P)H oxidase with apocynin decreased XO protein levels and prevented endothelial cell stimulation of [Formula: see text] production in response to oscillatory shear stress. These data suggest that the NAD(P)H oxidase maintains endothelial cell XO levels and that XO is responsible for increased reactive oxygen species production in response to oscillatory shear stress.<\/jats:p>","DOI":"10.1152\/ajpheart.00515.2003","type":"journal-article","created":{"date-parts":[[2015,3,3]],"date-time":"2015-03-03T20:15:00Z","timestamp":1425413700000},"page":"H2290-H2297","source":"Crossref","is-referenced-by-count":374,"title":["Role of xanthine oxidoreductase and NAD(P)H oxidase in endothelial superoxide production in response to oscillatory shear stress"],"prefix":"10.1152","volume":"285","author":[{"given":"J. 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