Abstract
Clinical manifestations of sickle cell disease are related to vaso-occlusive (VOC) events, which are responsible for acute and chronic organ damages. We have recently shown the beneficial effects of inhaled nitric oxide (NO) in both transgenic sickle cell (SAD) mice exposed to hypoxia/reoxygenation (H/R) and in sickle cell children with acute painful crisis (
In addition to histological lung damage, H/R induced an increase in blood neutrophils, a market increase in BAL total leukocyte and neutrophil counts, an increase in BAL IL-6 and IL-1β, with no significant changes in BAL IL-10 and TNF-α levels. PNA prevented the H/R lung injury, determined a reduction in H/R mediated increase in blood neutrophils, prevented the increase in BAL total leukocyte and neutrophil counts and in BAL IL-6 and IL-1β levels, while no change was observed in BAL IL-10, TNF-α and MetHb levels. hsAlb ameliorates the H/R lung injury but it did not affect either the H/R induced blood neutrophils, and BAL cells and cytokines. These results show that the beneficial effects of PNA are similar to those observed with inhaled NO and that PNA could be therapeutically efficacious in sickle cell disease.
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