Surgical animal models of heart failure related to coronary heart disease

被引:121
作者
Klocke, Rainer
Tian, Wen
Kuhlmann, Michael T.
Nikol, Sgrid
机构
[1] Univ Hosp Munster, Dept Cardiol & Angiol, Munster, Germany
[2] China Med Univ, Dept Cardiol, Hosp 1, Shenyang, Peoples R China
关键词
coronary heart disease; animal model; heart failure; myocardial infarction; ischemia/reperfusion;
D O I
10.1016/j.cardiores.2006.11.026
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coronary heart disease is caused by atherosclerotic narrowing of coronary arteries. It accounts for about two-thirds of heart failure cases, which are frequently secondary to myocardial infarction. Despite considerable progress in the understanding and management of heart failure, its incidence, prevalence and economic burden are steadily increasing. Therefore, efficient preventive and therapeutic measures are urgently needed. In order to investigate the mechanisms involved in the pathogenesis of coronary heart disease-related heart failure and to develop therapies, appropriate animal models are indispensable. According to the aetiology of this disorder, surgical models are based on various methods allowing for the narrowing or occlusion of coronary arteries. Depending on the duration and extent of the impairment of coronary blood flow and its consequences for cardiac tissue, these are classified as models of myocardial infarction, cardiac ischemia/reperfusion injury, or chronic cardiac ischemia. In addition, factors such as species, strain, and gender of the laboratory animals also significantly contribute to the pathophysiology of the induced disorder and, therefore, have to be taken into consideration thoroughly when an animal model is to be established. (c) 2006 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 38
页数:10
相关论文
共 69 条
[1]   Induction of myocardial infarcts of a predictable size and location by branch pattern probability-assisted coronary ligation in C57BL/6 mice [J].
Ahn, D ;
Cheng, L ;
Moon, C ;
Spurgeon, H ;
Lakatta, EG ;
Talan, MI .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2004, 286 (03) :H1201-H1207
[2]  
[Anonymous], 2005, EUROPEAN CARDIOVASCU
[3]   Involvement of FrzA/sFRP-1 and the Wnt/frizzled pathway in ischemic preconditioning [J].
Barandon, L ;
Dufourcq, P ;
Costet, P ;
Moreau, C ;
Allières, C ;
Daret, D ;
Dos Santos, P ;
Lamazière, JMD ;
Couffinhal, T ;
Duplàa, C .
CIRCULATION RESEARCH, 2005, 96 (12) :1299-1306
[4]   Improvement of left ventricular remodeling and function by hydroxymethylglutaryl coenzyme A reductase inhibition with cerivastatin in rats with heart failure after myocardial infarction [J].
Bauersachs, J ;
Galuppo, P ;
Fraccarollo, D ;
Christ, M ;
Ertl, G .
CIRCULATION, 2001, 104 (09) :982-985
[5]   Cardiac Na/Ca exchange function in rabbit, mouse and man: What's the difference? [J].
Bers, DM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (04) :369-373
[6]   AN ANIMAL-MODEL OF CHRONIC CORONARY STENOSIS RESULTING IN HIBERNATING MYOCARDIUM [J].
BOLUKOGLU, H ;
LIEDTKE, AJ ;
NELLIS, SH ;
EGGLESTON, AM ;
SUBRAMANIAN, R ;
RENSTROM, B .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :H20-H29
[7]  
BOND MG, 1980, AM J PATHOL, V101, P675
[8]   Dilated cardiomyopathy resulting from high-level myocardial expression of Cre-recombinase [J].
Buerger, A ;
Rozhitskaya, O ;
Sherwood, MC ;
Dorfman, AL ;
Bisping, E ;
Abel, ED ;
Pu, WT ;
Izumo, S ;
Jay, PY .
JOURNAL OF CARDIAC FAILURE, 2006, 12 (05) :392-398
[9]   VENTRICULAR REMODELING INDUCED BY ACUTE NONOCCLUSIVE CONSTRICTION OF CORONARY-ARTERY IN RATS [J].
CAPASSO, JM ;
JEANTY, MW ;
PALACKAL, T ;
OLIVETTI, G ;
ANVERSA, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (06) :H1983-H1993
[10]   NONISCHEMIC MYOCARDIAL DAMAGE INDUCED BY NONOCCLUSIVE CONSTRICTION OF CORONARY-ARTERY IN RATS [J].
CAPASSO, JM ;
LI, P ;
ANVERSA, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (03) :H651-H661