Nitric oxide (NO) is implicated in a wide variety of biological roles. NO i
s generated fi-om three nitric oxide synthase (NOS) isoforms: neuronal (nNO
S), inducible (iNOS), and endothelial (eNOS) all of which are found in the
lung. While there are no isoform-specific inhibitors of NOS, the recent dev
elopment and characterization of mice deficient in each of the NOS isoforms
has allowed for more comprehensive study of the importance of NO in the lu
ng circulation. Studies in the mouse have identified the role of NO from eN
OS in modulating pulmonary vascular tone and in attenuating the development
of chronic hypoxic pulmonary hypertension.