In vivo porcine model of reperfused myocardial infarction: In situ double staining to measure precise infarct area/area at risk

被引:51
作者
Suzuki, Yoriyasu [1 ]
Lyons, Jennifer K. [1 ]
Yeung, Alan C. [1 ]
Ikeno, Fumiaki [1 ]
机构
[1] Stanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA 94305 USA
关键词
myocardial infarction; animal model; coronary artery catheterization;
D O I
10.1002/ccd.21329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The aim of this study is to evaluate a catheter-based porcine model for reperfused myocardial infarction and investigate the appropriate location and duration of the occlusion. Material and Methods: A balloon catheter was placed in the left descending coronary artery (LAD) in 78 swine, and used to occlude the LAD. To evaluate this model, left ventricular ejection fraction (LVEF), infarct size, incidence of ventricular fibrillation (VF), and mortality was compared among three groups: 60-min proximal LAD occlusion (60P), 60-min mid LAD occlusion (60M), and 30-min proximal LAD occlusion (30P). Results: In 72 of the 78 pigs, the procedures were successfully completed. Both mortality and incidence of VF were highest in the 60P group (66.7% and 91.7%, respectively). Myocardial infarction was successfully induced in all 72 animals and in situ double-staining with Evans blue dye and 2,3,5-triphenyltetrazolium chloride was performed to delineate area at risk for ischemia and infarcted myocardium. There was no difference in infarct size, expressed as a percentage of the area at risk, between the 60P and 60M groups (49.5% +/- 3.9% vs. 45.4% +/- 13.3%, respectively). Serial changes in LVEF of the 60M group demonstrated that until 14 days after reperfusion, LVEF improved naturally over time (36.4% +/- 6.6% at 24 hr, and 47.3% +/- 10.1% at 14 days). Conclusion: This model and methodology could provide a reproducible and consistent infarct size. The current study demonstrated that 60-min mid LAD occlusion can be the most feasible to serve as a porcine reperfused myocardial infarction model. (c) 2008 Wiley-Liss, Inc.
引用
收藏
页码:100 / 107
页数:8
相关论文
共 26 条
[1]   A model of closed chest regional myocardial infarction in the rabbit:: a clinically relevant in vivo assay system of post-infarction remodelling [J].
Edwards, R ;
Yousef, Z ;
Rakhit, R ;
Wright, M ;
Rosenthal, E ;
Redwood, S ;
Marber, M .
BASIC RESEARCH IN CARDIOLOGY, 2002, 97 (05) :374-383
[2]   A CLOSED-CHEST PIG MODEL OF SUSTAINED VENTRICULAR-TACHYCARDIA [J].
ELDAR, M ;
OHAD, D ;
BOR, A ;
VARDABLOOM, N ;
SWANSON, DK ;
BATTLER, A .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 1994, 17 (10) :1603-1609
[3]  
FOZZARD HA, 1975, CIRCULATION S, V52, P31
[4]   INTRACORONARY ETHANOL ABLATION IN SWINE - EFFECTS OF ETHANOL CONCENTRATION ON LESION FORMATION AND RESPONSE TO PROGRAMMED VENTRICULAR STIMULATION [J].
HAINES, DE ;
WHAYNE, JG ;
DIMARCO, JP .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1994, 5 (05) :422-431
[5]   Impaired perfusion after myocardial infarction is due to reperfusion-induced δPKC-mediated myocardial damage [J].
Ikeno, Fumiaki ;
Inagaki, Koichi ;
Rezaee, Mehrdad ;
Mochly-Rosen, Daria .
CARDIOVASCULAR RESEARCH, 2007, 73 (04) :699-709
[6]   Cardioprotection by ε-protein kinase C activation from ischemia -: Continuous delivery and antiarrhythmic effect of an ε-protein kinase C-activating peptide [J].
Inagaki, K ;
Begley, R ;
Ikeno, F ;
Mochly-Rosen, D .
CIRCULATION, 2005, 111 (01) :44-50
[7]   Inhibition of δ-protein kinase C protects against reperfusion injury of the ischemic heart in vivo [J].
Inagaki, K ;
Chen, L ;
Ikeno, F ;
Lee, FH ;
Imahashi, K ;
Bouley, DM ;
Rezaee, M ;
Yock, PG ;
Murphy, E ;
Mochly-Rosen, D .
CIRCULATION, 2003, 108 (19) :2304-2307
[8]   OBSERVATIONS ON EXPERIMENTAL MYOCARDIAL ISCHEMIA [J].
KLONER, RA ;
BRAUNWALD, E .
CARDIOVASCULAR RESEARCH, 1980, 14 (07) :371-395
[9]   Minimally invasive method for creating coronary stenosis in a swine model for MRI and SPECT imaging [J].
Kraitchman, DL ;
Bluemke, DA ;
Chin, BB ;
Heldman, AW ;
Heldman, AW .
INVESTIGATIVE RADIOLOGY, 2000, 35 (07) :445-451
[10]  
Krombach GA, 2005, INVEST RADIOL, V40, P14