REDUCTION OF CANINE MYOCARDIAL INFARCT SIZE BY CI-959, AN INHIBITOR OF INFLAMMATORY CELL ACTIVATION

被引:12
作者
BURKE, SE [1 ]
WRIGHT, CD [1 ]
POTOCZAK, RE [1 ]
BOUCHER, DM [1 ]
DODD, GD [1 ]
TAYLOR, DG [1 ]
KAPLAN, HR [1 ]
机构
[1] WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV, CARDIOVASC SECT, DEPT PHARMACOL, ANN ARBOR, MI USA
关键词
MYOCARDIAL INFARCT SIZE; CELL ACTIVATION INHIBITOR; REPERFUSION INJURY; ANESTHETIZED DOG; OXYGEN FREE RADICALS; NEUTROPHILS;
D O I
10.1097/00005344-199210000-00016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CI-959, a cell-activation inhibitor that prevents the formation of oxygen-derived free radicals by inflammatory cells, was studied to determine its effects on myocardial infarct size and subsequent scar formation in dogs. The left circumflex coronary artery was occluded for 90 min, followed by 6 h of reperfusion. Drug infusion was started 15 min before reperfusion at a loading dose of 8 mg/kg i.v., followed immediately by 2 mg/kg i.v. infused over 80 min. The infarct size, assessed by TTC staining techniques, was significantly reduced in 12 dogs treated with CI-959 (23.3 +/- 3.6% of the area at risk) when compared to 11 vehicle-treated animals (35.5 +/- 4% of the area at risk, p < 0.05). This reduction in infarct size was not attributed to changes in regional myocardial blood flow, as measured by radioactive microspheres, or to a reduction in myocardial oxygen demand, as estimated by changes in the rate-pressure product. The scar thickness, measured after a 6-week recovery period in 9 animals treated with CI-959, was not significantly reduced in comparison with 11 controls. In vitro, CI-959 effectively inhibited oxygen free radical formation by canine neutrophils. The results of this study show that CI-959 significantly reduces the myocardial infarct size without causing scar thinning, which might lead to ventricular aneurysm, and suggests the most likely mechanism for its beneficial action is the prevention of formation of toxic oxygen radicals.
引用
收藏
页码:619 / 629
页数:11
相关论文
共 41 条
[1]   REDUCTION IN EXPERIMENTAL INFARCT SIZE BY RECOMBINANT HUMAN SUPEROXIDE-DISMUTASE - INSIGHTS INTO THE PATHOPHYSIOLOGY OF REPERFUSION INJURY [J].
AMBROSIO, G ;
BECKER, LC ;
HUTCHINS, GM ;
WEISMAN, HF ;
WEISFELDT, ML .
CIRCULATION, 1986, 74 (06) :1424-1433
[2]   BIOLOGICAL DEFENSE MECHANISMS - PRODUCTION BY LEUKOCYTES OF SUPEROXIDE A POTENTIAL BACTERICIDAL AGENT [J].
BABIOR, BM ;
KIPNES, RS ;
CURNUTTE, JT .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (03) :741-744
[3]   EFFECTS OF FREE-RADICALS ON THE FLUIDITY OF MYOCARDIAL MEMBRANES [J].
BAGCHI, M ;
PRASAD, MR ;
ENGELMAN, RM ;
DAS, DK .
FREE RADICAL RESEARCH COMMUNICATIONS, 1989, 7 (3-6) :375-380
[4]   NAFAZATROM-INDUCED SALVAGE OF ISCHEMIC MYOCARDIUM IN ANESTHETIZED DOGS IS MEDIATED THROUGH INHIBITION OF NEUTROPHIL FUNCTION [J].
BEDNAR, M ;
SMITH, B ;
PINTO, A ;
MULLANE, KM .
CIRCULATION RESEARCH, 1985, 57 (01) :131-141
[5]   VENTRICULAR SEPTAL RUPTURE DURING IBUPROFEN THERAPY FOR PERICARDITIS AFTER ACUTE MYOCARDIAL-INFARCTION [J].
BODEN, WE ;
SADANIANTZ, A .
AMERICAN JOURNAL OF CARDIOLOGY, 1985, 55 (13) :1631-1632
[6]   SCAR THINNING DUE TO IBUPROFEN ADMINISTRATION AFTER EXPERIMENTAL MYOCARDIAL-INFARCTION [J].
BROWN, EJ ;
KLONER, RA ;
SCHOEN, FJ ;
HAMMERMAN, H ;
HALE, S ;
BRAUNWALD, E .
AMERICAN JOURNAL OF CARDIOLOGY, 1983, 51 (05) :877-883
[7]   MYOCARDIAL ALTERATIONS DUE TO FREE-RADICAL GENERATION [J].
BURTON, KP ;
MCCORD, JM ;
GHAI, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (06) :H776-H783
[8]   EFFECT OF SUPEROXIDE-DISMUTASE ON MYOCARDIAL INFARCT SIZE IN THE CANINE HEART AFTER 6 HOURS OF REGIONAL ISCHEMIA AND REPERFUSION - A DEMONSTRATION OF MYOCARDIAL SALVAGE [J].
CHI, L ;
TAMURA, Y ;
HOFF, PT ;
MACHA, M ;
GALLAGHER, KP ;
SCHORK, MA ;
LUCCHESI, BR .
CIRCULATION RESEARCH, 1989, 64 (04) :665-675
[9]   CANINE NEUTROPHIL ACTIVATION BY CARDIAC LYMPH OBTAINED DURING REPERFUSION OF ISCHEMIC MYOCARDIUM [J].
DREYER, WJ ;
SMITH, CW ;
MICHAEL, LH ;
ROSSEN, RD ;
HUGHES, BJ ;
ENTMAN, ML ;
ANDERSON, DC .
CIRCULATION RESEARCH, 1989, 65 (06) :1751-1762
[10]  
GILLESPIE MN, 1986, J PHARMACOL EXP THER, V239, P836