Objective: To investigate the effect of sepsis on the intestinal absor
ption of arginine. Design: Controlled, nonintervention study. Setting:
Surgical research laboratories of Sinai Hospital of Baltimore, Subjec
ts: Male Sprague-Dawley rats. Interventions: Experimental sepsis induc
ed by cecal ligation and puncture or intraperitoneal injection of lipo
polysaccharide. Measurements and Main Results: Sepsis assessed by peri
toneal and blood cultures. Intestinal absorption estimated by measurin
g the transfer of H-3-arginine by everted jejunal sacs prepared from s
eptic and control animals (n = 6 per group) at multiple time points af
ter the induction of sepsis (6, 12, 24, 48, and 72 hrs after cecal lig
ation and puncture; 6 and 12 hrs after intraperitoneal injection of li
popolysaccharide), Induction of peritonitis in the rat by cecal ligati
on and puncture significantly reduced the in vitro uptake of arginine
by everted jejunal sacs at 12, 24, and 48 hrs after laparotomy, Argini
ne transfer by everted jejunal sacs was also significantly reduced in
rats as early as 6 hrs after intraperitoneal injection of endotoxin (e
ndotoxin 273 +/- 14; saline 377 +/- 14 nmol/sac/hr). Data are expresse
d as mean +/- SEM, Recovery from sepsis was associated with normalizat
ion of arginine transfer by intestinal sacs. Conclusions: Experimental
sepsis, induced by either cecal ligation and puncture or intraperiton
eal injection of lipopolysaccharide, resulted in impaired intestinal a
mino acid uptake. Impaired intestinal arginine absorption may explain
the lack of benefit of enteral, compared with parenteral, arginine the
rapy on survival from a septic insult.