Paigen B, Morrow A, Holmes P A, Mitchell D, Williams R A
Bruce Lyon Memorial Research Laboratory, Children's Hospital Medical Center, Oakland, CA 94609.
Atherosclerosis. 1987 Dec;68(3):231-40. doi: 10.1016/0021-9150(87)90202-4.
The well-defined genetic systems of the mouse are proving useful in experimental studies of atherosclerosis. Inbred mouse strains differ in atherosclerosis susceptibility, and several variants of apolipoproteins have been identified and mapped. This report explores the location and timing of lesion formation in the mouse in an effort to provide a basis for quantitatively comparing groups of mice. After 14 weeks on an atherogenic diet containing 1.25% cholesterol, 15% fat, and 0.5% cholic acid, C57BL/6J female mice had aortic lesions at each of the intercostal arteries, at the junction of the aorta to the heart, and in scattered areas covering 1.1% +/- 0.5 (SD) of the aortic surface. After 9 months on the atherogenic diet, those lesions near the heart and intercostal arteries were extensive, 8% +/- 3 (SD) of the remainder of the aorta was involved in lesions, and lesions were found in the coronary arteries. Results indicated that one suitable location for scoring lesions was in a 300 micron area of the aorta just beyond the aortic sinus. The mean number of lesions/mouse in the selected area after 14 weeks on the atherogenic diet was 1.1 +/- 0.3 (SD). The results were reproducible over 10 separate experiments. The number of lesions per mouse fit a Poisson distribution indicating that the presence of one lesion did not predispose the mouse to acquiring a second lesion. Lesion formation and cholesterol levels did not vary with the season of the year as demonstrated by 9 separate experiments over more than 12 months. Methods of evaluating the number and size of lesions were compared including sizing with a microscope eyepiece grid and computer-assisted planimetry. The resulting data provide reproducible methods of quantitatively comparing lesion formation in various strains or groups of mice, thereby increasing the usefulness of the mouse as an experimental system for atherosclerosis research.
事实证明,小鼠明确的遗传系统在动脉粥样硬化实验研究中很有用。近交系小鼠品系在动脉粥样硬化易感性方面存在差异,并且已经鉴定和定位了几种载脂蛋白变体。本报告探讨了小鼠病变形成的位置和时间,以便为定量比较小鼠组提供依据。在含有1.25%胆固醇、15%脂肪和0.5%胆酸的致动脉粥样化饮食喂养14周后,C57BL/6J雌性小鼠的肋间动脉、主动脉与心脏交界处以及覆盖主动脉表面1.1%±0.5(标准差)的散在区域出现了主动脉病变。在致动脉粥样化饮食喂养9个月后,心脏和肋间动脉附近的病变广泛,主动脉其余部分的8%±3(标准差)出现病变,并且在冠状动脉中也发现了病变。结果表明,一个合适的病变评分位置是主动脉窦后方300微米的主动脉区域。在致动脉粥样化饮食喂养14周后,所选区域每只小鼠的平均病变数为1.1±0.3(标准差)。该结果在10次独立实验中具有可重复性。每只小鼠的病变数符合泊松分布,这表明一个病变的存在不会使小鼠更容易出现第二个病变。超过12个月的9次独立实验表明,病变形成和胆固醇水平不会随一年中的季节而变化。比较了评估病变数量和大小的方法,包括使用显微镜目镜网格和计算机辅助平面测量法进行测量。所得数据提供了定量比较不同品系或小鼠组病变形成的可重复方法,从而提高了小鼠作为动脉粥样硬化研究实验系统的实用性。