Background. Some studies have suggested that the addition of arginine to en
teral feeding solutions may improve outcome in critically ill patients, but
the mechanism is incompletely explained. In particular, the availability a
nd utilization of arginine administered enterally is not wen defined. Metho
ds: This prospective, randomized, double-blind, placebo-controlled study pe
rformed in a Department of Medicosurgical Intensive Care included 51 patien
ts likely requiring long-term enteral feeding. Thirty-seven patients (57 +/
- 7 years, SAPS II 33 +/- 6) completed the 7-day study, of whom 20 received
the formula enriched with free arginine (6.3 g/L) and 17 received an isoca
loric and isonitrogenous control solution. Arginine absorption was assessed
from plasma arginine concentrations in serial samples. Three pathways of a
rginine utilization were explored: (1) the production of nitric oxide, asse
ssed by the plasma concentration of nitrite/nitrate (NOx) and citrulline, a
nd 24-hour urinary excretion of NOx; (2) the protein turnover, estimated by
the phenylalanine concentrations; and (3) the activity of arginase, reflec
ted by the ornithine concentration. Results: The plasma concentrations of a
rginine and ornithine increased in the group fed with the enriched formula
(from 55 +/- 9 mu mol/L to 102 +/- 9 mu mol/L and from 57 +/- 7 to 135 +/-
11 mu mol/L, respectively, p < .05), but not with the control formula. Ther
e was no difference between groups in either NO production or phenylalanine
concentration. Conclusions: Supplemental arginine in enteral feeding is re
adily absorbed, and mainly metabolized into ornithine, presumably by the ar
ginase enzyme.