Abstract
Clinical trials of inhaled nitrite to treat pulmonary arterial hypertension (PAH) are ongoing. The pathogenesis of PAH involves smooth muscle hypertrophy as a result of endothelial dysfunction and/or chronic vasoconstriction. Nitric oxide (NO) is a potent vasodilator and a primary therapeutic pathway for PAH. This review will address some of the emerging PAH treatment strategies utilizing the NO pathway.
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CITATION STYLE
APA
Simon, M. A. (2014). Nitric Oxide Therapeutics in Pulmonary Vascular Disease. Advances in Pulmonary Hypertension, 13(3), 134–137. https://doi.org/10.21693/1933-088x-13.3.134
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