Why the study?
Does inhaled nitric oxide inhibit platelet aggregation in healthy volunteers?
Does inhaled nitric oxide inhibit platelet aggregation in healthy volunteers?
Inhaled nitric oxide significantly inhibits platelet aggregation and prolongs in vitro bleeding time in healthy volunteers at concentrations as low as 5 ppm.
May warrant bleeding monitoring with inhaled NO; extends antiplatelet effects to low-dose inhalation in an RCT.
The platelet inhibitory effect of 0-40 ppm inhaled nitric oxide (NO) was investigated in healthy men and women. In both groups, ADP-and collagen-induced platelet aggregation was significantly inhibited 20 (T20) and 40 min (T40) after the beginning of inhalation of 5, 10, and 40 ppm. Moreover, in both men and women, the in vitro bleeding time was significantly prolonged at T20 and T40 during inhalation of 40 ppm. Inhalation of NO also inhibited P-selectin expression at 5, 10, and 40 ppm and fibrinogen binding to the GPIIb/IIIa-receptor at 40 ppm. In conclusion, in healthy volunteers, the platelet inhibitory effect of inhaled NO was not dose-related, since it was significant at 5 and 10 ppm but did not increase during the administration of higher NO concentrations. In addition, gender-related differences were only observed in ADP-induced platelet aggregation at 10 ppm and in bleeding time prolongation at 40 ppm.
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A 2000 study studied this question.
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