Nitric Oxide Metabolites in Sickle Cell Anemia Patients after Oral Administration of Hydroxyurea

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Abstract
The mechanism of action of hydroxyurea (HU) in decreasing the frequency of pain crisis in sickle cell disease (SCD) has not been fully elucidated. In vitro and in vivo studies suggest that nitric oxide (NO), a potent vasodilator, may partly be responsible for the beneficial effect of HU. This study was designed to determine the effect of oral administration of HU on plasma levels of NO metabolites (NOx) in sickle cell patients (SCP). The results indicate that during steady-state plasma levels of NOx were significantly higher in HU-treated patients compared to non HU-treated patients or normal controls (p <.05). In five inpatients in mild pain plasma levels of NOx increased significantly after 2h of HU administration (p <.05); however, in three inpatients in persistent pain with significantly lower baseline NOx there was a minimal NOx response to HU at 2h (p <.01). These observations indicate that HU administration is associated with the production of NO in some SCP, but that further study of the pharmacodynamics of this effect is necessary.