EFFECTS OF U74006F, A NOVEL INHIBITOR OF LIPID-PEROXIDATION, IN STUNNED REPERFUSED CANINE MYOCARDIUM

被引:45
作者
HOLZGREFE, HH
BUCHANAN, LV
GIBSON, JK
机构
[1] Cardiovascular Diseases Research, Upjohn Company, Kalamazoo, MI
关键词
Function recovery; Stunned myocardium; U74006F;
D O I
10.1097/00005344-199002000-00010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
U74006F, a novel 21-amino steroid is a potent inhibitor of iron-mediated lipid peroxidation and has been shown to be of therapeutic benefit in central nervous system ischemia. As oxygen radicals have been implicated in the development of postischemic myocardial dysfunction, we examined the efficacy of U74006F to enhance the recovery of function in a canine model of stunned, reperfused myocardium. Twenty-six dogs were randomized to either a vehicle (n = 11), U74006F (n = 10), or U74006F-paced group (n = 5). U74006F (6 mg/kg i.v.) was administered 15 min prior to coronary artery occlusion. Myocardial blood flows were measured by the microsphere technique, and function data were obtained by sonomicrometry. Both U74006F-treated groups demonstrated a significant increase in posterior wall thickening as compared to the vehicle treatment (U74006F-paced, 27.0 12.8%; U74006F, 22.4 ± 11%; vehicle, -13.5 ± 9.9%, p < 0.001 following 3 h of reperfusion). Enhanced function recovery was accompanied by lower heart rates in the U74006F-treated group following reperfusion (treated versus vehicle, 109 ± 6.7 versus 131 ± 8.8 beats/min, p = 0.004). The U74006F-paced group was maintained at the same rate as the vehicle group, with no diminution in function recovery compared to the unpaced group. No effects in systemic hemodynamics or nutrient blood flow were evident as a function of drug treatment. We conclude that pretreatment with U74006F enhances the recovery of function in stunned canine myocardium via the inhibition of oxygen radicals and lipid peroxidation products. This activity suggests that this compound represents a new therapeutic adjunct in reperfusion and recanalization therapies. © 1990 Raven Press, Ltd., New York.
引用
收藏
页码:239 / 248
页数:10
相关论文
共 52 条
[1]   EVIDENCE FOR A REVERSIBLE OXYGEN RADICAL MEDIATED COMPONENT OF REPERFUSION INJURY - REDUCTION BY RECOMBINANT HUMAN SUPEROXIDE-DISMUTASE ADMINISTERED AT THE TIME OF REFLOW [J].
AMBROSIO, G ;
WEISFELDT, ML ;
JACOBUS, WE ;
FLAHERTY, JT .
CIRCULATION, 1987, 75 (01) :282-291
[2]  
ARMITAGE P, 1977, STATISTICAL METHODS, P189
[3]   THE EFFECT OF ALLOPURINOL ON THE DEGREE OF EARLY MYOCARDIAL ISCHEMIA [J].
ARNOLD, WL ;
DEWALL, RA ;
KEZDI, P ;
ZWART, HHJ .
AMERICAN HEART JOURNAL, 1980, 99 (05) :614-624
[4]  
AUST S D, 1985, Journal of Free Radicals in Biology and Medicine, V1, P3, DOI 10.1016/0748-5514(85)90025-X
[5]   MYOCARDIAL CONSEQUENCES OF REPERFUSION [J].
BECKER, LC ;
AMBROSIO, G .
PROGRESS IN CARDIOVASCULAR DISEASES, 1987, 30 (01) :23-44
[6]   INTRINSIC WASHOUT RATES OF TL-201 IN NORMAL AND ISCHEMIC MYOCARDIUM AFTER DIPYRIDAMOLE-INDUCED VASODILATION [J].
BELLER, GA ;
HOLZGREFE, HH ;
WATSON, DD .
CIRCULATION, 1985, 71 (02) :378-386
[7]  
BERNE RM, 1977, CARDIOVASCULAR PHYSL, P155
[8]   DEMONSTRATION OF FREE-RADICAL GENERATION IN STUNNED MYOCARDIUM OF INTACT DOGS WITH THE USE OF THE SPIN TRAP ALPHA-PHENYL N-TERT-BUTYL NITRONE [J].
BOLLI, R ;
PATEL, BS ;
JEROUDI, MO ;
LAI, EK ;
MCCAY, PB .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (02) :476-485
[9]  
BRAUGHLER JM, 1987, J BIOL CHEM, V262, P10438
[10]  
BRAUGHLER JM, 1988, J PHARMACOL EXP THER, V244, P423