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To study the effect of lung bypass on the production of prostaglandin E2, prostacyclin, and thromboxane A2, we measured simultaneously arterial and venous plasma concentrations of prostaglandin E2, 6-keto-prostaglandin F1 alpha (stable metabolite of prostacyclin), and thromboxane B2 (stable metabolite of thromboxane A2) before, during, and after cardiopulmonary bypass. Seventeen patients (age range 46 to 69 years) undergoing aorta-coronary bypass grafts were investigated. The prostaglandin E2 production rose sharply immediately after the onset of bypass (baseline: 9.7 +/- 2.9 pg/ml to 85 +/- 16.6 pg/ml in venous and 87 +/- 12 pg/ml in arterial plasma, p less than 0.03) and rapidly decreased after pulmonary reperfusion (53 +/- 6.4 and 57 +/- 20 pg/ml, respectively, in venous and arterial plasma at the end of bypass). The increase in prostaglandin E2 was influenced by the heart-lung machine itself (as demonstrated by a closed "bypass" circuit) and by lung bypass. Pulmonary metabolism of prostaglandin E2 was maintained after bypass. The prostacyclin production rose significantly at the beginning of bypass (154 +/- 26 pg/ml venous prebypass level to 361 +/- 94 pg/ml after aortic clamping, p less than 0.03). Prostacyclin decreased progressively during rewarming of the patient, pulmonary reperfusion, and discontinuation of bypass. When prostacyclin decreased, thromboxane B2 production rose significantly and reached peak arterial levels when the lungs were reperfused (112 +/- 33 pg/ml prebypass levels to 402 +/- 101 pg/ml, p less than 0.01). Except for prostaglandin E2, there were no significant differences between arterial and venous plasma levels of these substances. The same prostanoids were also measured in five patients undergoing major orthopedic operations, and no significant changes in prostanoids were observed. Our data demonstrate significant production of prostaglandin E2 in the systemic circulation during cardiopulmonary bypass in humans. They further indicate that lung bypass disturbs the plasma prostaglandin/thromboxane balance.
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
August 1982,
The Journal of thoracic and cardiovascular surgery,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
August 1981,
The Journal of thoracic and cardiovascular surgery,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
March 1995,
The Annals of thoracic surgery,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
March 1983,
Journal of periodontal research,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
January 1995,
ASAIO journal (American Society for Artificial Internal Organs : 1992),
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
August 1985,
The Annals of thoracic surgery,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
January 1980,
Transactions - American Society for Artificial Internal Organs,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
April 1983,
Prostaglandins,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
July 1986,
The Journal of thoracic and cardiovascular surgery,
M E Faymonville, and
G Deby-Dupont, and
R Larbuisson, and
C Deby, and
L Bodson, and
R Limet, and
M Lamy
January 1980,
Transactions - American Society for Artificial Internal Organs,
