S. Wan et al., MYOCARDIUM IS A MAJOR SOURCE OF PROINFLAMMATORY CYTOKINES IN PATIENTSUNDERGOING CARDIOPULMONARY BYPASS, Journal of thoracic and cardiovascular surgery, 112(3), 1996, pp. 806-811
Proinflammatory cytokines, such as tumor necrosis factor-alpha, interl
eukin-6, and interleukin-8, and antiinflammatory cytokines, such as in
terleukin-10, may play an important role in patient responses to cardi
opulmonary bypass. We sought to define whether the myocardium and the
lungs serve as important sources of these cytokines under conditions o
f cardiopulmonary bypass. Ten patients (age 64 +/- 3 years, mean +/- s
tandard error of the mean) undergoing elective coronary artery bypass
grafting were monitored with an arterial catheter, a coronary sinus ca
theter, and a pulmonary artery catheter. Plasma levels of tumor necros
is factor-a, interleukin-6, interleukin-8, and interleukin-10 were mea
sured simultaneously in peripheral arterial blood, coronary sinus bloo
d, and mixed venous blood before heparin administration, 1 minute befo
re aortic crossclamping, 5 minutes after aortic declamping, and at 0.5
, 1, 1.5 and 2 hours after aortic declamping. The durations of cardiop
ulmonary bypass and aortic crossclamping were 114 +/- 9 and 64 +/- 5 m
inutes, respectively. Levels of tumor necrosis factor-alpha and interl
eukin-6 were significantly higher in coronary sinus blood than in arte
rial blood after aortic declamping. Tumor necrosis factor-a and interl
eukin-6 levels were also higher in mixed venous blood than in arterial
blood within 1 hour after declamping. There were no significant diffe
rences among the three sampling sites with respect to interleukin-8 an
d interleukin-10 levels. In one patient who had postoperative myocardi
al infarction, however, interleukin-8 levels were three times as high
as in coronary sinus blood than in arterial blood. These data indicate
that the myocardium is a major source of tumor necrosis factor-a and
interleukin-6 in patients undergoing cardiopulmonary bypass. The lungs
may consume rather than release proinflammatory cytokines in the earl
y phase of reperfusion. The source under these conditions of the antii
nflammatory cytokine interleukin-10 remains to be determined.