C57BL/6 mice fed high fat diets as models for diabetes-accelerated atherosclerosis

被引:156
作者
Schreyer, SA [1 ]
Wilson, DL [1 ]
LeBoeuf, RC [1 ]
机构
[1] Univ Washington, Dept Med & Nutr Sci, Seattle, WA 98195 USA
关键词
mice; atherosclerosis; diabetes; dietary fat;
D O I
10.1016/S0021-9150(97)00165-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Non-insulin-dependent diabetes mellitus (NIDDM) is a major risk factor for the development of atherosclerosis in humans. The development of an animal model that displays accelerated atherosclerosis associated with NIDDM will aid in elucidating the mechanisms that associate these disorders. C57BL/6 mice may provide such a model system. This strain becomes obese, hyperglycemic and insulin resistant when fed a high fat diet (diabetogenic diet) and is susceptible to atherosclerotic lesion development when fed a separate high fat diet containing cholesterol and bile acids (atherogenic diet). This report tests whether a diet commonly used to induce atherosclerosis also provokes a diabetic phenotype and whether a diet used to induce diabetes provokes the development of aortic fatty streak lesions. Mice of strains C57BL/6, C3H/He, BALB/c and seven recombinant inbred (RI) strains were fed an atherogenic diet for 14 weeks and glucose parameters were measured. No correlation was observed between atherosclerosis susceptibility and fasting insulin or glucose levels, or glucose clearance following short-term insulin or glucose treatment. Analysis of the RI strains suggested that multiple genes control these glucose metabolic parameters. Feeding the diabetogenic diet for 14 weeks to C57BL/6 mice induced obesity and diabetes and 2-fold increases in plasma lipoprotein concentrations. Also, small aortic sinus lipid deposits were observed in 40% of the mice. Thus, analysis of the diabetogenic diet fed C57BL/6 mouse may provide an important tool for further studies of diabetes accelerated vascular disease. (C) 1998 Elsevier Science Ireland Ltd.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 23 条
[1]   ESTIMATES OF INVIVO INSULIN ACTION IN MAN - COMPARISON OF INSULIN TOLERANCE-TESTS WITH EUGLYCEMIC AND HYPERGLYCEMIC GLUCOSE CLAMP STUDIES [J].
BONORA, E ;
MOGHETTI, P ;
ZANCANARO, C ;
CIGOLINI, M ;
QUERENA, M ;
CACCIATORI, V ;
CORGNATI, A ;
MUGGEO, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (02) :374-378
[2]   MORBIDITY AND MORTALITY IN DIABETICS IN FRAMINGHAM POPULATION - 16-YEAR FOLLOW-UP STUDY [J].
GARCIA, MJ ;
MCNAMARA, PM ;
GORDON, T ;
KANNELL, WB .
DIABETES, 1974, 23 (02) :105-111
[3]   DIETARY-FAT INCREASES HIGH-DENSITY-LIPOPROTEIN (HDL) LEVELS BOTH BY INCREASING THE TRANSPORT RATES AND DECREASING THE FRACTIONAL CATABOLIC RATES OF HDL CHOLESTEROL ESTER AND APOLIPOPROTEIN (APO) A-I - PRESENTATION OF A NEW ANIMAL-MODEL AND MECHANISTIC STUDIES IN HUMAN APO A-I TRANSGENIC AND CONTROL MICE [J].
HAYEK, T ;
ITO, Y ;
AZROLAN, N ;
VERDERY, RB ;
AALTOSETALA, K ;
WALSH, A ;
BRESLOW, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) :1665-1671
[4]  
JIAO S, 1990, J LIPID RES, V31, P467
[5]   GENETIC-ANALYSIS OF GLUCOSE-TOLERANCE IN INBRED MOUSE STRAINS - EVIDENCE FOR POLYGENIC CONTROL [J].
KAKU, K ;
FIEDOREK, FT ;
PROVINCE, M ;
PERMUTT, MA .
DIABETES, 1988, 37 (06) :707-713
[6]  
KIRK EA, 1995, J LIPID RES, V36, P1522
[7]   CORONARY HEART-DISEASE INCIDENCE IN NIDDM PATIENTS IN THE HELSINKI HEART-STUDY [J].
KOSKINEN, P ;
MANTTARI, M ;
MANNINEN, V ;
HUTTUNEN, JK ;
HEINONEN, OP ;
FRICK, MH .
DIABETES CARE, 1992, 15 (07) :820-825
[8]   Increased atherosclerosis in Streptozotocin-induced diabetic mice [J].
Kunjathoor, VV ;
Wilson, DL ;
LeBoeuf, RC .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) :1767-1773
[9]  
LEBOEUF RC, 1994, J LIPID RES, V35, P121
[10]   GENETIC-CONTROL OF INFLAMMATORY GENE INDUCTION AND NF-KAPPA-B-LIKE TRANSCRIPTION FACTOR ACTIVATION IN RESPONSE TO AN ATHEROGENIC DIET IN MICE [J].
LIAO, F ;
ANDALIBI, A ;
DEBEER, FC ;
FOGELMAN, AM ;
LUSIS, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2572-2579