A Cloned Pig Model for Examining Atherosclerosis Induced by High Fat, High Cholesterol Diets

被引:22
作者
Jensen, Tor W. [1 ]
Mazur, Meredith J. [2 ]
Pettigew, James E. [2 ]
Perez-Mendoza, Victor G. [2 ]
Zachary, James [3 ]
Schook, Lawrence B. [1 ,2 ]
机构
[1] Univ Illinois, Inst Genom Biol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Anim Sci, Urbana, IL 61801 USA
[3] Univ Illinois, Coll Vet Med, Dept Pathobiol, Urbana, IL 61801 USA
关键词
Atherosclerosis; Cholesterol; Cloned pig; Diet; IMPROVED HEART FUNCTION; MYOCARDIAL-INFARCTION; APOLIPOPROTEIN-E; CELL TRANSPLANTATION; TRANSENDOCARDIAL DELIVERY; COLLATERAL CIRCULATION; PORCINE MODEL; ANGIOGENESIS; PERFUSION; ISCHEMIA;
D O I
10.1080/10495398.2010.490693
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The pig is a recognized model for the onset of coronary heart disease and heart attacks. Previous studies have shown that serum cholesterol levels in the pig can be elevated using a high fat, high cholesterol (HFHC) diet. What has been lacking is a genetically defined model corresponding to human ApoE4 susceptibility that can be linked to diets capable of inducing atherosclerosis. This study used a cloned pig model to examine the impact of cholesterol levels with the development of aorta fatty deposits leading to atherosclerosis. Diets were formulated using vegetable sources of protein to provide similar intakes of metabolizable energy, calcium, phosphorous and principal amino acids in both control and HFHC groups. After 60 days, the HFHC group demonstrated a 40-fold increase in aortic fatty streak lesion area combined with 6- and 11-fold increases in total and LDL cholesterol, respectively, over control diet fed cloned pigs. Previous studies have suffered from either imbalanced total caloric intake, an overall imbalance in the nutrition of the control versus HFHC groups or genetic heterogeneity when evaluating dietary constraints related to atherosclerosis. This study demonstrated that cloned, genetically-defined ApoE4 pigs provided balanced nutrition diets provide an experimental system ideally suited to examining atherosclerosis and the onset of coronary heart disease.
引用
收藏
页码:179 / 187
页数:9
相关论文
共 25 条
[1]   EVIDENCE FOR AN ALTERED LIPID METABOLIC STATE IN CIRCULATING BLOOD MONOCYTES UNDER CONDITIONS OF HYPERLIPEMIA IN SWINE AND ITS IMPLICATIONS IN ARTERIAL LIPID-METABOLISM [J].
BELL, FP ;
GERRITY, RG .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (02) :155-162
[2]   THE SEQUENCE OF PORCINE APOLIPOPROTEIN-E (APOE) CDNA [J].
BRZOZOWSKA, A ;
GRIMHOLT, U ;
KULSETH, MA ;
WOLD, I ;
ROGNE, S .
DNA SEQUENCE, 1993, 4 (03) :207-210
[3]  
DAOUD AS, 1981, ARCH PATHOL LAB MED, V105, P233
[4]   Apolipoprotein E and atherosclerosis: insight from animal and human studies [J].
Davignon, J ;
Cohn, JS ;
Mabile, L ;
Bernier, L .
CLINICA CHIMICA ACTA, 1999, 286 (1-2) :115-143
[5]   Dyslipidemia and vascular dysfunction in diabetic pigs fed an atherogenic diet [J].
Dixon, JL ;
Stoops, JD ;
Parker, JL ;
Laughlin, MH ;
Weisman, GA ;
Sturek, M .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (12) :2981-2992
[6]   Transendocardial delivery of autologous bone marrow enhances collateral perfusion and regional function in pigs with chronic experimental myocardial ischemia [J].
Fuchs, S ;
Baffour, R ;
Zhou, YF ;
Shou, M ;
Pierre, A ;
Tio, FO ;
Weissman, NJ ;
Leon, MB ;
Epstein, SE ;
Kornowski, R .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (06) :1726-1732
[7]   The elusive coypu: the importance of collateral flow and the search for an alternative to the dog [J].
Hearse, DJ .
CARDIOVASCULAR RESEARCH, 2000, 45 (01) :215-219
[8]   Translational Physiology: Porcine models of human coronary artery disease: implications for preclinical trials of therapeutic angiogenesis [J].
Hughes, GC ;
Post, MJ ;
Simons, M ;
Annex, BH .
JOURNAL OF APPLIED PHYSIOLOGY, 2003, 94 (05) :1689-1701
[9]   RECENT ADVANCES IN MOLECULAR PATHOLOGY - ANIMAL-MODELS IN ATHEROSCLEROSIS RESEARCH [J].
JOKINEN, MP ;
CLARKSON, TB ;
PRICHARD, RW .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1985, 42 (01) :1-28
[10]   Effect of catheter-based transendocardial delivery of stromal cell-derived factor 1α on left ventricular function and perfusion in a porcine model of myocardial infarction [J].
Koch, KC ;
Schaefer, WM ;
Liehn, EA ;
Rammos, C ;
Mueller, D ;
Schroeder, J ;
Dimassi, T ;
Stopinski, T ;
Weber, C .
BASIC RESEARCH IN CARDIOLOGY, 2006, 101 (01) :69-77