ARGININE DEFICIENCY ACCOMPANIES PERSISTENT PULMONARY-HYPERTENSION OF THE NEWBORN

Citation
Rj. Vosatka et al., ARGININE DEFICIENCY ACCOMPANIES PERSISTENT PULMONARY-HYPERTENSION OF THE NEWBORN, Biology of the neonate, 66(2-3), 1994, pp. 65-70
Citations number
29
Categorie Soggetti
Pediatrics
Journal title
ISSN journal
00063126
Volume
66
Issue
2-3
Year of publication
1994
Pages
65 - 70
Database
ISI
SICI code
0006-3126(1994)66:2-3<65:ADAPPO>2.0.ZU;2-T
Abstract
Persistent pulmonary hypertension of the newborn (PPHN) is a life-thre atening disorder of neonates manifested by vasoconstriction of the pul monary arteries. Recently, the gas nitric oxide (NO) has been used wit h some success in the management of infants with PPHN. Exogenous admin istration of NO selectively dilates the pulmonary vascular bed. NO is naturally synthesized in the body from the amino acid L-arginine. Here we report our findings that infants with PPHN are deficient in argini ne and achieve normal or elevated plasma arginine concentrations with intravenous hyperalimentation. We prospectively identified and studied 10 infants with PPHN who were not receiving protein or amino acids fo r at least 24 h and compared their plasma arginine concentrations to 8 control infants without PPHN given similar nutrition. Plasma arginine concentrations were 32 +/- 14 and 52 +/- 20 mu mol/l in infants with PPHN and control infants, respectively (p = 0.02). There were no other statistically significant differences in plasma amino acid concentrat ion for any of the 22 other amino acids determined. Infants with PPHN who were subsequently treated with amino acid infusions had plasma arg inine concentrations of 115 +/- 48 mu mol/l (mean often determinations at 86 +/- 27 h after initiation of intravenous amino acids in five PP HN infants).