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(Circulation Research. 1995;76:215-222.)
© 1995 American Heart Association, Inc.

Articles

Continuous Nitric Oxide Inhalation Reduces Pulmonary Arterial Structural Changes, Right Ventricular Hypertrophy, and Growth Retardation in the Hypoxic Newborn Rat

Jesse D. Roberts, Jr, Carole T. Roberts, Rosemary C. Jones, Warren M. Zapol, Kenneth D. Bloch

From the Departments of Anaesthesia (J.D.R., R.C.J., W.M.Z.), Pediatrics (J.D.R.), and Medicine (K.D.B.) and the Cardiovascular Research Center (J.D.R., C.T.R., K.D.B.), Harvard Medical School at Massachusetts General Hospital, Boston.

Abstract Breathing low oxygen levels for several weeks produces progressive pulmonary artery hypertension and smooth muscle hypertrophy and hyperplasia in many species. Because nitric oxide (NO) is an important regulator of pulmonary vascular tone, we examined whether the continuous inhalation of low levels of NO gas would attenuate pulmonary arterial structural changes in hypoxic rat pups. Nine-day-old rat pups and their mothers continuously breathed at FIO₂ 0.21 or 0.10 with or without adding 20 ppm (by volume) NO for 2 weeks. Lung tissue was obtained for vascular morphometric analysis, and the hearts were dissected to measure right ventricular weight and levels of mRNA encoding rat atrial natriuretic factor (rANF). In addition, femur and skull length were radiographically determined. Breathing at FIO₂ 0.10 for 14 days increased pulmonary arterial wall thickness and the proportion of muscular arteries in the lung periphery. Right ventricular weight and right ventricular rANF gene expression increased, whereas body weight and skeletal growth were reduced (all P<.05). Continuous inhalation of 20 ppm NO at FIO₂ 0.10 for 2 weeks decreased hypoxic pulmonary vascular structural changes and somatic growth retardation and prevented the increase of right ventricular weight and right ventricular rANF mRNA levels. These observations suggest that chronically breathing NO attenuates pulmonary vascular smooth muscle hypertrophy and/or hyperplasia and extension into distal arterial walls, right ventricular hypertrophy, and growth retardation of newborns breathing at a low oxygen level.

Key Words: pulmonary artery hypertension • congenital heart disease • nitric oxide • newborn rats

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