Nitric Oxide in Treatment of Persistent Pulmonary Hypertension of the Newborn

The gas nitric oxide (NO) inhaled in very low concentrations, for approximately a day or two, appears to be lifesaving in infants with persistent pulmonary hypertension of the newborn (PPHN). It is, indeed, remarkable that an oxide of nitrogen, a precursor to toxic nitrogen oxides often found in polluted air, is effective against this potentially le thal neonatal disorder. We are beginning to under stand that the basis for its effectiveness lies in the facts that the pulmonary hypertension is caused by a virulent form of smooth muscle constriction within pulmonary arterioles and that NO is an ex tremely powerful relaxant of smooth muscle, even in picomolar concentrations. Often, when an im portant biologic function is performed by an ex tremely small amount of an agent, the agent is re lated to a control mechanism normally used by the body. Such is the case for NO, which is normally produced by the endothelial lining cells of the ar teries and quickly diffuses into the smooth muscle layer where it reduces vascular tone. Because the control of vascular tone and hence the diameter of blood vessels is of crucial importance for blood cir culation, health, not only of the neonate, but of us all, may depend in part on the proper function of the NO system. Although our understanding of the chemistry, physiology, pharmacology, and patho physiology of NO has only recently developed, we cannot forget the heritage we owe to earlier medi cal researchers.

[1]  E. Shaffer,et al.  Clinical responses to prolonged treatment of persistent pulmonary hypertension of the newborn with low doses of inhaled nitric oxide. , 1993, The Journal of pediatrics.

[2]  E. Shaffer,et al.  Low-dose inhalational nitric oxide in persistent pulmonary hypertension of the newborn , 1992, The Lancet.

[3]  Jesse D. Roberts,et al.  Inhaled nitric oxide in persistent pulmonary hypertension of the newborn , 1992, The Lancet.

[4]  S. Abman,et al.  Hemodynamic effects of exogenous nitric oxide in ovine transitional pulmonary circulation. , 1992, The American journal of physiology.

[5]  D. Cornfield,et al.  Effects of birth-related stimuli on L-arginine-dependent pulmonary vasodilation in ovine fetus. , 1992, The American journal of physiology.

[6]  S. Archer,et al.  Direct role for potassium channel inhibition in hypoxic pulmonary vasoconstriction. , 1992, The American journal of physiology.

[7]  S. Moncada,et al.  Nitric oxide: physiology, pathophysiology, and pharmacology. , 1991, Pharmacological reviews.

[8]  D. Rodman,et al.  Maturational changes in endothelium-derived relaxing factor activity of ovine pulmonary arteries in vitro. , 1991, The American journal of physiology.

[9]  S. Abman,et al.  Role of endothelium-derived relaxing factor during transition of pulmonary circulation at birth. , 1990, The American journal of physiology.

[10]  F. Accurso,et al.  Failure of postnatal adaptation of the pulmonary circulation after chronic intrauterine pulmonary hypertension in fetal lambs. , 1989, The Journal of clinical investigation.

[11]  C. Lundgren,et al.  Development of pulmonary vascular response to oxygen. , 1988, The American journal of physiology.

[12]  F. Accurso,et al.  Temporal Response of the Fetal Pulmonary Circulation to Pharmacologic Vasodilators , 1988, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[13]  V. Miller,et al.  Modulation of endothelium-dependent responses by chronic alterations of blood flow. , 1986, The American journal of physiology.

[14]  R. Furchgott,et al.  The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine , 1980, Nature.

[15]  M. Prinzmetal,et al.  Angina pectoris. I. A variant form of angina pectoris; preliminary report. , 1959, The American journal of medicine.

[16]  T. Brunton ON THE USE OF NITRITE OF AMYL IN ANGINA PECTORIS. , 1867 .

[17]  F. Accurso,et al.  Sustained fetal pulmonary vasodilation with prolonged atrial natriuretic factor and GMP infusions. , 1991, The American journal of physiology.

[18]  K. Stenmark,et al.  Etiologic mechanisms in persistent pulmonary hypertension of the newborn , 1989 .

[19]  R. Furchgott Endothelium-Dependent Relaxation in Systemic Arteries , 1988 .