Key result
Intra-arterial application of aqueous nitric oxide increased forearm blood flow in a dose-dependent manner from 2.8 to 13.5 ml/min/100 ml tissue, demonstrating transport in a bioactive form.
Why the study?
Does intra-arterial aqueous nitric oxide solution increase downstream forearm blood flow and radial artery diameter in healthy volunteers?
Does intra-arterial aqueous nitric oxide solution increase downstream forearm blood flow and radial artery diameter in healthy volunteers?
Absolute Event Rate: 13.5% vs 2.8%
p-value: p=<0.05
Authentic nitric oxide can be transported in bioactive form for significant distances along the vascular bed, challenging the dogma that it acts strictly as a local vasodilator.
Challenges local-only NO dogma; leaves open distant vascular signaling for future mechanistic and therapeutic studies.
Although hitherto considered as a strictly locally acting vasodilator, results from recent clinical studies with inhaled nitric oxide (NO) indicate that NO can exert effects beyond the pulmonary circulation.We therefore sought to investigate potential remote vascular effects of intra-arterially applied aqueous NO solution and to identify the mechanisms involved.On bolus application of NO into the brachial artery of 32 healthy volunteers, both diameter of the downstream radial artery and forearm blood flow increased in a dose-dependent manner.Maximum dilator responses were comparable to those after stimulation of endogenous NO formation with acetylcholine and bradykinin.Response kinetics and pattern of NO decomposition suggested that despite the presence of hemoglobin-containing erythrocytes, a significant portion of NO was transported in its unbound form.Infusion of NO (36 mol/min) into the brachial artery increased levels of plasma nitroso species, nitrite, and nitrate in the draining antecubital vein (by < 2-fold, 30-fold, and 4-fold, respectively), indicative of oxidative and nitrosative chemistry.Infused N-oxides were inactive as vasodilators whereas S-nitrosoglutathione dilated conduit and resistance arteries.Our results suggest that NO can be transported in bioactive form for significant distances along the vascular bed.Both free NO and plasma nitroso species contribute to the dilation of the downstream vasculature.
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Rassaf et al. (2002) studied Healthy volunteers (n=32). Aqueous nitric oxide (NO) solution vs. Saline (0.9% NaCl) was evaluated on Forearm blood flow (FBF) (p=<0.05). Intra-arterial application of aqueous nitric oxide increased forearm blood flow in a dose-dependent manner from 2.8 to 13.5 ml/min/100 ml tissue, demonstrating transport in a bioactive form.
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