Animal models of dilated cardiomyopathy for translational research

被引:52
作者
Recchia, F. A. [1 ]
Lionetti, V.
机构
[1] Scuola Sup Sant Anna, Sect Med, Pisa, Italy
[2] Inst Clin Physiol, Pisa, Italy
[3] New York Med Coll, Dep Physiol, Valhalla, NY USA
关键词
dilated cardiomyopathy; experimental animal models; heart failure;
D O I
10.1007/s11259-007-0005-8
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Animal models of cardiovascular disease have proved critically important for the discovery of pathophysiological mechanisms and for the advancement of diagnosis and therapy. They offer a number of advantages, principally the availability of adequate healthy controls and the absence of confounding factors such as marked differences in age, concomitant pathologies and pharmacological treatments. Dilated cardiomyopathy (DCM) is the third cause of heart failure (HF) and is characterized by progressive ventricular dilation and functional impairment in the absence of coronary lesions and/or hypertension. Over the past thirty years, investigators have developed numerous small and large animal models to study this very complex syndrome. Genetically modified mice are the most widely and intensively utilized research animals and allow high throughput studies on DCM. However, to translate discoveries from basic science into medical applications, research in large animal models becomes a necessary step. An accurate large animal model of DCM is pacing-induced HF. It is obtained by continuous cardiac pacing at a frequency three- to fourfold higher than the spontaneous heart rate and is mostly applied to dogs, but also to pigs, sheep and monkeys. To date, this model can still be considered a gold standard in HF research.
引用
收藏
页码:35 / 41
页数:7
相关论文
共 30 条
[1]   Dissociation between regional dysfunction and β-adrenergic receptor signaling in heart failure [J].
Anzai, T ;
Lai, NC ;
Gao, MH ;
Hammond, HK .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 275 (04) :H1267-H1273
[2]   RAPID VENTRICULAR PACING IN THE DOG - PATHOPHYSIOLOGIC STUDIES OF HEART-FAILURE [J].
ARMSTRONG, PW ;
STOPPS, TP ;
FORD, SE ;
DEBOLD, AJ .
CIRCULATION, 1986, 74 (05) :1075-1084
[3]   Learning from failure: congestive heart failure in the postgenomic age [J].
Benjamin, IJ ;
Schneider, MD .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (03) :495-499
[4]   Quantifying the heart failure epidemic: prevalence, incidence rate, lifetime risk and prognosis of heart failure - The Rotterdam Study [J].
Bleumink, GS ;
Knetsch, AM ;
Sturkenboom, MCJM ;
Straus, SMJM ;
Hofman, A ;
Deckers, JW ;
Witteman, JCM ;
Stricker, BHC .
EUROPEAN HEART JOURNAL, 2004, 25 (18) :1614-1619
[5]   Myocardial protection at a crossroads - The need for translation into clinical therapy [J].
Bolli, R ;
Becker, L ;
Gross, G ;
Mentzer, R ;
Balshaw, D ;
Lathrop, DA .
CIRCULATION RESEARCH, 2004, 95 (02) :125-134
[6]   Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. [J].
Felker, GM ;
Thompson, RE ;
Hare, JM ;
Hruban, RH ;
Clemetson, DE ;
Howard, DL ;
Baughman, KL ;
Kasper, EK .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (15) :1077-1084
[7]   Increased sensitivity of vascular smooth muscle to nitric oxide in dilated cardiomyopathy of syrian hamsters (Bio TO-2 strain) [J].
Goineau, S ;
Pape, D ;
Guillo, P ;
Ramée, MP ;
Bellissant, E .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2001, 37 (03) :290-300
[8]   Frequency and phenotypes of familial dilated cardiomyopathy [J].
Grünig, E ;
Tasman, JA ;
Kücherer, H ;
Franz, W ;
Kübler, W ;
Katus, HA .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (01) :186-194
[9]   Expression profiling of human idiopathic dilated cardiomyopathy [J].
Grzeskowiak, R ;
Witt, H ;
Drungowski, M ;
Thermann, R ;
Hennig, S ;
Perrot, A ;
Osterziel, KJ ;
Klingbiel, D ;
Scheid, S ;
Spang, R ;
Lehrach, H ;
Ruiz, P .
CARDIOVASCULAR RESEARCH, 2003, 59 (02) :400-411
[10]   Experimental models for the study of cardiovascular function and disease [J].
Hearse, DJ ;
Sutherland, FJ .
PHARMACOLOGICAL RESEARCH, 2000, 41 (06) :597-603