Schreyer S A, Wilson D L, LeBoeuf R C
Department of Medicine and Nutritional Sciences, University of Washington, Seattle 98195-3410, USA.
Atherosclerosis. 1998 Jan;136(1):17-24. doi: 10.1016/s0021-9150(97)00165-2.
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.
非胰岛素依赖型糖尿病(NIDDM)是人类动脉粥样硬化发生的主要危险因素。建立一种表现出与NIDDM相关的加速动脉粥样硬化的动物模型,将有助于阐明与这些疾病相关的机制。C57BL/6小鼠可能提供这样一种模型系统。当喂食高脂肪饮食(致糖尿病饮食)时,该品系会变得肥胖、血糖升高并产生胰岛素抵抗,而当喂食含有胆固醇和胆汁酸的单独高脂肪饮食(致动脉粥样硬化饮食)时,易发生动脉粥样硬化病变。本报告测试了一种常用于诱导动脉粥样硬化的饮食是否也会引发糖尿病表型,以及一种用于诱导糖尿病的饮食是否会引发主动脉脂肪条纹病变的发展。给C57BL/6、C3H/He、BALB/c品系的小鼠以及七个重组近交(RI)品系的小鼠喂食致动脉粥样硬化饮食14周,并测量血糖参数。未观察到动脉粥样硬化易感性与空腹胰岛素或血糖水平,或短期胰岛素或葡萄糖治疗后的血糖清除率之间存在相关性。对RI品系的分析表明,多个基因控制这些葡萄糖代谢参数。给C57BL/6小鼠喂食致糖尿病饮食14周会导致肥胖和糖尿病,并使血浆脂蛋白浓度增加两倍。此外,在40%的小鼠中观察到小主动脉窦脂质沉积。因此,对喂食致糖尿病饮食的C57BL/6小鼠的分析可能为进一步研究糖尿病加速血管疾病提供重要工具。