Granulocyte Superoxide Anion and Elastase Release During Cardiopulmonary Bypass
- 1 October 1993
- journal article
- Published by Wiley in Artificial Organs
- Vol. 17 (10) , 837-842
- https://doi.org/10.1111/j.1525-1594.1993.tb00391.x
Abstract
Cardiopulmonary bypass (CPB) is known to induce several pathogenic responses in cardiovascular surgery. To explore leukocyte activation during PCB, we investigated superoxide anion (O2‐) production by granulocytes in 6 patients undergoing aortocoronary bypass surgery. O2‐ production was determined with chemiluminescence amplified by a cypridina luciferin analogue. Granulocytes collected from the blood in the arterial site of the CPB circuit were stimulated by phorbol myristate acetate, n‐formyl‐methionyl‐leucyl‐phenylalanine, and opsonized zymosan. All the stimulators failed to disclose a significant difference between the magnitude of chemiluminescence during and after CPB. However, significant complement activation was detected, and the plasma level of granulocyte elastase increased gradually during and after CPB. This discrepancy between the unchanged O2‐ production by stimulated granulocytes and the increase in inflammatory mediators including granulocyte elastase may be due to sequestration of activated granulocytes in extravascular tissues. Namely, it was highly likely that activated granulocytes responsible for the increased plasma elastase level were sequestered and remained outside the blood circulation.Keywords
This publication has 27 references indexed in Scilit:
- Lung injury and complement activation: Role of neutrophils and xanthine oxidaseFree Radical Biology & Medicine, 1991
- Formation of C5a during cardiopulmonary bypass: Inhibition by precoating with heparinThe Annals of Thoracic Surgery, 1991
- Complement activation and lung permeability during cardiopulmonary bypassThe Annals of Thoracic Surgery, 1990
- A prospective study of the risk of an immediate adverse reaction to protamine sulfate during cardiopulmonary bypass surgeryJournal of Allergy and Clinical Immunology, 1990
- Changes in Neutrophil Oxidative Potential in Patients Undergoing Cardiopulmonary Bypass with Polypropylene Hollow Fiber OxygenatorsArtificial Organs, 1990
- Complement Activation in Cardiopulmonary Bypass, with Special Reference to Anaphylatoxin Production in Membrane and Bubble OxygenatorsThe Annals of Thoracic Surgery, 1988
- Neutrophil-mediated injury to endothelial cells. Enhancement by endotoxin and essential role of neutrophil elastase.Journal of Clinical Investigation, 1986
- Neutrophils degrade subendothelial matrices in the presence of alpha-1-proteinase inhibitor. Cooperative use of lysosomal proteinases and oxygen metabolites.Journal of Clinical Investigation, 1984
- The respiratory burst of phagocytes.Journal of Clinical Investigation, 1984
- Complement Activation during Cardiopulmonary BypassNew England Journal of Medicine, 1981