Objective: To study the effects of increasing dosages of epinephrine given
intravenously on intestinal oxygen supply and, in particular, mucosal tissu
e oxygen tension in an autoperfused, innervated jejunal segment.
Design: Prospective, randomized experimental study.
Setting: Animal research laboratory.
Subjects: Domestic pigs.
Interventions: Sixteen pigs were anesthetized, paralyzed, and normoventilat
ed. A small segment of the jejunal mucosa was exposed by midline laparotomy
and antimesenteric incision. Mucosal oxygen tension was measured by using
Clark-type surface oxygen electrodes. Microvascular hemoglobin oxygen satur
ation and microvascular blood flow (perfusion units) were determined by tis
sue reflectance spectrophotometry and laser-Doppler velocimetry. Systemic h
emodynamics, mesenteric-venous acid-base and blood gas variables, and syste
mic acid-base and blood gas variables were recorded. Measurements were perf
ormed after a resting period and at 20-min intervals during infusion of inc
reasing dosages of epinephrine (n = 8; 0.01, 0.05, 0.1,0.5, 1, and 2 mug kg
-l min-l) or without treatment (n = 8). In addition, arterial and mesenteri
c-venous lactate concentrations were measured at baseline and at 60 and 120
mins.
Measurements and Main Results: Epinephrine infusion led to significant tach
ycardia; an increase in cardiac output, systemic oxygen delivery, and oxyge
n consumption; and development of lactic acidosis. Epinephrine significantl
y increased jejunal microvascular blood flow (baseline, 267 +/- 39 perfusio
n units; maximum value, 443 +/- 35 perfusion units) and mucosal oxygen tens
ion (baseline, 36 +/- 2.0 torr [4.79 +/- 0.27 kPa]; maximum value, 48 +/- 2
.8 torr [6.39 +/- 0.37 kPa]) and increased hemoglobin oxygen saturation abo
ve baseline. Epinephrine increased mesenteric venous lactate concentration
(baseline, 2.9 +/- 0.6 mmol.L-1; maximum value, 5.5 +/- 0.2 mmol.L-1) witho
ut development of an arterial-mesenteric venous lactate concentration gradi
ent.
Conclusions: Epinephrine increased jejunal microvascular blood flow and muc
osal tissue oxygen supply at moderate to high dosages. Lactic acidosis that
develops during infusion of increasing dosages of epinephrine is not relat
ed to development of gastrointestinal hypoxia.