A MONOCLONAL-ANTIBODY TO P-SELECTIN AMELIORATES INJURY ASSOCIATED WITH HEMORRHAGIC-SHOCK IN RABBITS

被引:31
作者
WINN, RK
PAULSON, JC
HARLAN, JM
机构
[1] UNIV WASHINGTON, DEPT SURG, SEATTLE, WA 98195 USA
[2] UNIV WASHINGTON, DEPT MED, SEATTLE, WA 98195 USA
[3] UNIV WASHINGTON, DEPT PHYSIOL BIOPHYS, SEATTLE, WA 98195 USA
[4] CYTEL CORP, SAN DIEGO, CA 92121 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1994年 / 267卷 / 06期
关键词
LEUKOCYTE ADHESION MOLECULES; NEUTROPHILS; CD18; CD62P;
D O I
10.1152/ajpheart.1994.267.6.H2391
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P-selectin (CD62P) can participate in leukocyte rolling when it is expressed on the surface of endothelial cells. We examined the role of CD62P in hemorrhagic shock and resuscitation. Rabbits were treated with saline, an anti-CD62P (alpha-CD62P) monoclonal antibody (MAb; PB1.3), an isotype-matched hSAb (PNB1.6), or an alpha-CD18 MAb (60.3). Catheters were placed in the femoral artery and vein for monitoring, and cardiac output was then reduced to 33% of baseline for 1.5 h. Shed blood was returned, and resuscitation was continued to maintain the cardiac output to within 90% of baseline. There were no statistical differences between the saline- and MAb PNB1.6-treated groups; they were therefore combined into a control group. The MAb PB1.3- and MAb 60.3-treated groups required significantly less fluid resuscitation than the controls (12, 17, and 56 ml/kg, respectively). We conclude that MAbs directed to functional epitopes of either CD62P or CD18 provide significant protection from vascular injury after hemorrhagic shock.
引用
收藏
页码:H2391 / H2397
页数:7
相关论文
共 42 条
[1]   PROTECTIVE EFFECTS OF DILTIAZEM AND RYANODINE AGAINST ISCHEMIA-REPERFUSION INJURY IN NEONATAL RABBIT HEARTS [J].
AKITA, T ;
ABE, T ;
KATO, S ;
KODAMA, I ;
TOYAMA, J .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1993, 106 (01) :55-66
[2]  
ARFORS KE, 1987, BLOOD, V69, P338
[3]  
Baker SP., 1992, THE INJURY FACT BOOK, V2
[4]   GRANULOCYTES AND NO-REFLOW PHENOMENON IN IRREVERSIBLE HEMORRHAGIC-SHOCK [J].
BARROSOARANDA, J ;
SCHMIDSCHONBEIN, GW ;
ZWEIFACH, BW ;
ENGLER, RL .
CIRCULATION RESEARCH, 1988, 63 (02) :437-447
[5]   CIRCULATING NEUTROPHIL KINETICS DURING TOLERANCE IN HEMORRHAGIC-SHOCK USING BACTERIAL LIPOPOLYSACCHARIDE [J].
BARROSOARANDA, J ;
CHAVEZCHAVEZ, RH ;
MATHISON, JC ;
SUEMATSU, M ;
SCHMIDSCHONBEIN, GW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02) :H415-H421
[6]   TRANSFORMATION OF NEUTROPHILS AS INDICATOR OF IRREVERSIBILITY IN HEMORRHAGIC-SHOCK [J].
BARROSOARANDA, J ;
SCHMIDSCHONBEIN, GW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (03) :H846-H852
[7]  
BARROSOARANDA J, 1992, CIRC SHOCK, V36, P185
[8]  
BEATTY PG, 1983, J IMMUNOL, V131, P2913
[9]   SIALYL LEWIS(X)-CONTAINING OLIGOSACCHARIDE ATTENUATES MYOCARDIAL REPERFUSION INJURY IN CATS [J].
BUERKE, M ;
WEYRICH, AS ;
ZHENG, ZL ;
GAETA, FCA ;
FORREST, MJ ;
LEFER, AM .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (03) :1140-1148
[10]   PROTEOLYSIS BY NEUTROPHILS - RELATIVE IMPORTANCE OF CELL-SUBSTRATE CONTACT AND OXIDATIVE INACTIVATION OF PROTEINASE-INHIBITORS INVITRO [J].
CAMPBELL, EJ ;
SENIOR, RM ;
MCDONALD, JA ;
COX, DL .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (04) :845-852