Inhibition of the metabolism of endogenous
atrial natriuretic peptide (
ANP), by continuous infusion of a specific inhibitor of
neutral endopeptidase (membrane
metalloendopeptidase E.C. 3.4.24.11), UK 73,967 (
candoxatrilat), was undertaken in rats, in which chronic
hypoxia was used as a stimulus to induce
pulmonary hypertension and
right ventricular hypertrophy. Inhibition of
neutral endopeptidase 24.11 with low-dose and high-dose UK 73,967 (NEI) increased endogenous plasma
ANP by greater than 155% during the development of
pulmonary hypertension. NEI treatment reduced mean pulmonary arterial pressure in
hypoxia as follows: vehicle 26.6 +/- 4.0 mm Hg; low-dose NEI 22.7 +/- 1.9 mm Hg, and high-dose NEI 22.6 +/- 2.5 mm Hg (both p less than 0.01 compared with hypoxic vehicle); however, it was without effect on pulmonary arterial pressure in normoxia (17.6 +/- 2.2 mm Hg) or on systemic blood pressure. The development of
right ventricular hypertrophy was also reduced in both groups treated with NEI (right ventricular weight/left ventricular weight: 0.43 +/- 0.03 vehicle; 0.40 +/- 0.02 low-dose NEI and 0.40 +/- 0.02 high-dose NEI, both p less than 0.05 compared with vehicle). Remodelling of the pulmonary vasculature, characterized by extension of the muscle within the small pulmonary arteries toward the periphery of the lung, was reduced by NEI treatment (percentage of thick-walled peripheral vessels; 19.2 +/- 3.1% vehicle; 10.4 +/- 2.3% low-dose NEI and 8.1 +/- 1.8% high-dose NEI, both p less than 0.001 compared with vehicle). In the isolated blood perfused rat lung pulsed doses of NEI had no effect on pulmonary vascular tone in the absence of
ANP. Specific inhibition of the
enzyme neutral endopeptidase reduces vascular remodelling, the development of
pulmonary hypertension, and
right ventricular hypertrophy. Endogenous
ANP modulates vascular remodelling in vivo. Retarding the metabolism of endogenous
ANP through inhibition of
neutral endopeptidase 24.11 represents a potential approach toward
therapy. g