Expression of soluble endothelial adhesion molecules in clinical cardiopulmonary bypass

被引:19
作者
Galea, Joseph [1 ]
Rebuck, Naomi [2 ]
Finn, Adam [2 ]
Manche, Alex [3 ]
Moat, Neil [1 ]
机构
[1] Univ Sheffield, Cardiac Sci Sect, Sheffield, S Yorkshire, England
[2] Univ Sheffield, Dept Child Hlth, Sheffield, S Yorkshire, England
[3] No Gen Hosp, Dept Cardiothorac Surg, Sheffield, S Yorkshire, England
来源
PERFUSION-UK | 1998年 / 13卷 / 05期
关键词
D O I
10.1177/026765919801300506
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Soluble endothelial adhesion molecule expression in clinical cardiopulmonary bypass (CPB) was investigated. Neutrophil-mediated endothelial injury plays an important role in CPB-induced organ dysfunction. The adhesion of neutrophil to the endothelium is central to this process. It has been well documented that CPB induces neutrophil activation and changes in neutrophil adhesion molecule expression, but the effect of CPB on endothelial cell activation is not known. This study was designed to measure soluble endothelial adhesion molecules during CPB. We made serial measurements (by specific enzyme-linked immunoabsorbent assay) of plasma levels of the soluble endothelial adhesion molecules, ICAM-1 and E-selectin in patients undergoing routine CPB (n = 7) and in a control group (thoracotomy, n = 3). The results show an initial significant decrease during CPB followed by an increase in plasma E-selectin from 29.3 +/- 5.1 ng/ml (mean +/- SEM) prebypass to 34.0 +/- 5.4 ng/ml at 48 h postbypass. Likewise, plasma ICAM-1 significantly decreased during CPB and then increased from 246.3 +/- 38.0 ng/ml before bypass to 324.8 +/- 25.0 ng/ml and 355.0 +/- 23.0 ng/ml at 24 and 48 h after bypass, respectively. The rise in levels is statistically significant (p < 0.05). This study shows a decrease in circulating ICAM-1 and soluble E-selectin during CPB and an increase in their levels at 48 h after CPB.
引用
收藏
页码:314 / 321
页数:8
相关论文
共 44 条
[1]   INTERLEUKIN-1 ACTS ON CULTURED HUMAN VASCULAR ENDOTHELIUM TO INCREASE THE ADHESION OF POLYMORPHONUCLEAR LEUKOCYTES, MONOCYTES, AND RELATED LEUKOCYTE CELL-LINES [J].
BEVILACQUA, MP ;
POBER, JS ;
WHEELER, ME ;
COTRAN, RS ;
GIMBRONE, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (05) :2003-2011
[2]   IDENTIFICATION OF AN INDUCIBLE ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE [J].
BEVILACQUA, MP ;
POBER, JS ;
MENDRICK, DL ;
COTRAN, RS ;
GIMBRONE, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9238-9242
[3]   ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE-1 - AN INDUCIBLE RECEPTOR FOR NEUTROPHILS RELATED TO COMPLEMENT REGULATORY PROTEINS AND LECTINS [J].
BEVILACQUA, MP ;
STENGELIN, S ;
GIMBRONE, MA ;
SEED, B .
SCIENCE, 1989, 243 (4895) :1160-1165
[4]   Hypothermic versus normothermic cardiopulmonary bypass: Influence on circulating adhesion molecules [J].
Boldt, J ;
Osmer, C ;
Linke, LC ;
Gorlach, G ;
Hempelmann, G .
JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA, 1996, 10 (03) :342-347
[5]   CIRCULATING ADHESION MOLECULES IN PEDIATRIC CARDIAC-SURGERY [J].
BOLDT, J ;
OSMER, C ;
LINKE, LC ;
DAPPER, F ;
HEMPELMANN, G .
ANESTHESIA AND ANALGESIA, 1995, 81 (06) :1129-1135
[6]   CYTOKINE RESPONSES TO CARDIOPULMONARY BYPASS WITH MEMBRANE AND BUBBLE OXYGENATION [J].
BUTLER, J ;
CHONG, GL ;
BAIGRIE, RJ ;
PILLAI, R ;
WESTABY, S ;
ROCKER, GM .
ANNALS OF THORACIC SURGERY, 1992, 53 (05) :833-838
[7]   ROLE OF CYTOKINES IN THE PATHOGENESIS OF CARDIOPULMONARY-INDUCED MULTISYSTEM ORGAN FAILURE [J].
CASEY, LC .
ANNALS OF THORACIC SURGERY, 1993, 56 (05) :S92-S96
[8]   THROMBOXANE-A(2) MEDIATES PULMONARY-HYPERTENSION AFTER CARDIOPULMONARY BYPASS IN THE RABBIT [J].
CAVE, AC ;
MANCHE, A ;
DERIAS, NW ;
HEARSE, DJ .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1993, 106 (06) :959-967
[9]   INDUCTION AND DETECTION OF A HUMAN-ENDOTHELIAL ACTIVATION ANTIGEN INVIVO [J].
COTRAN, RS ;
GIMBRONE, MA ;
BEVILACQUA, MP ;
MENDRICK, DL ;
POBER, JS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (02) :661-666
[10]   THE ROLE OF CYTOKINES IN HEMOLYTIC TRANSFUSION REACTIONS [J].
DAVENPORT, RD .
IMMUNOLOGICAL INVESTIGATIONS, 1995, 24 (1-2) :319-331