A characterization of myocardial infarction induced by thrombotic occlusion and a comparison with mechanical ligation of the rat coronary artery

被引:2
作者
Ikeda, Y [1 ]
Umemura, K [1 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Pharmacol, Hamamatsu, Shizuoka 4313192, Japan
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 2001年 / 23卷 / 01期
关键词
coronary artery; myocardial infarction; rat; thrombosis;
D O I
10.1358/mf.2001.23.1.619176
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study we examined two different methods for inducing myocardial infarction in rats. We previously developed an animal model of coronary artery thrombotic occlusion induced by a photochemical reaction, which occurs when rose bengal (a photosensitizer dye) is injected into the animal and is irritated with green light. Arterial occlusion is thereby achieved nonmechanically. Using this method, we investigated the effect of thrombolytic intervention on myocardial infarct size. Infarct size was determined 24 h after the induction of myocardial infarction. When tisokinase (3mg/kg), a native tissue-type plasminogen activator, was administered 3 min after the ST-segment elevation on a lead II electrocardiogram, the infarct size was 20.6 +/- 5.1%, which was significantly smaller than that of control rats (37.3 +/- 4.6%). When tisokinase was administered 10 min after ST-segment elevation, the infarct size was 27.1 +/- 2.1%, which was significantly smaller than that of controls. The rat coronary artery thrombosis model incorporates many aspects of coronary thrombosis. it differs from the coronary ligation model in that it lends itself to the study of thrombolytic agents on animal models of myocardial infarction. (C) 2001 Prous Science. All rights reserved.
引用
收藏
页码:23 / 28
页数:6
相关论文
共 11 条
[1]   PREVALENCE OF TOTAL CORONARY-OCCLUSION DURING THE EARLY HOURS OF TRANSMURAL MYOCARDIAL-INFARCTION [J].
DEWOOD, MA ;
SPORES, J ;
NOTSKE, R ;
MOUSER, LT ;
BURROUGHS, R ;
GOLDEN, MS ;
LANG, HT .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (16) :897-902
[2]  
FUKUCHI M, 1992, N-S ARCH PHARMACOL, V346, P550
[3]   INTERMITTENT CORONARY-OCCLUSION IN ACUTE MYOCARDIAL-INFARCTION - VALUE OF COMBINED THROMBOLYTIC AND VASODILATOR THERAPY [J].
HACKETT, D ;
DAVIES, G ;
CHIERCHIA, S ;
MASERI, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (17) :1055-1059
[4]   AN EXPERIMENTAL MYOCARDIAL-INFARCTION MODEL IN THE RAT AND ITS PROPERTIES [J].
HIRATA, Y ;
UMEMURA, K ;
UEMATSU, T ;
NAKASHIMA, M .
JAPANESE JOURNAL OF PHARMACOLOGY, 1995, 67 (01) :51-57
[5]   Increased cerebral infarction by cyclic flow reductions: studies in the guinea pig MCA thrombosis model [J].
Kawano, KI ;
Ikeda, Y ;
Kondo, K ;
Umemura, K .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 275 (05) :R1578-R1583
[6]   THE TRANSIENT NATURE OF THE EFFECT OF ISCHEMIC PRECONDITIONING ON MYOCARDIAL INFARCT SIZE AND VENTRICULAR ARRHYTHMIA [J].
LI, YW ;
WHITTAKER, P ;
KLONER, RA .
AMERICAN HEART JOURNAL, 1992, 123 (02) :346-353
[7]   ISCHEMIC PRECONDITIONING PROTECTS AGAINST INFARCTION IN RAT-HEART [J].
LIU, YG ;
DOWNEY, JM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (04) :H1107-H1111
[8]   CONSEQUENCES OF REOCCLUSION AFTER SUCCESSFUL REPERFUSION THERAPY IN ACUTE MYOCARDIAL-INFARCTION [J].
OHMAN, EM ;
CALIFF, RM ;
TOPOL, EJ ;
CANDELA, R ;
ABBOTTSMITH, C ;
ELLIS, S ;
SIGMON, KN ;
KEREIAKES, D ;
GEORGE, B ;
STACK, R .
CIRCULATION, 1990, 82 (03) :781-791
[9]  
SANIABADI AR, 1995, THROMB HAEMOSTASIS, V73, P868
[10]  
SELYE H., 1960, ANGIOLOGY, V11, P398, DOI 10.1177/000331976001100505