Li Ling, Cao Dongfeng, Garber David W, Kim Helen, Fukuchi Ken-ichiro
Departments of Medicine, Pharmacology, and Genetics, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Am J Pathol. 2003 Dec;163(6):2155-64. doi: 10.1016/s0002-9440(10)63572-9.
High fat/high cholesterol diets exacerbate beta-amyloidosis in mouse models of Alzheimer's disease (AD). It has been impossible, however, to study the relationship between atherosclerosis and beta-amyloidosis in those models because such mice were on atherosclerosis-resistant genetic backgrounds. Here we report the establishment of AD model mice, B6Tg2576, that are prone to atherosclerosis. B6Tg2576 mice were produced by back-crossing Tg2576 mice, an AD mouse model overexpressing human amyloid beta-protein precursor with the Swedish double mutation, to C57BL/6 mice, a strain susceptible to diet-induced atherosclerosis. An atherogenic diet induced aortic atherosclerosis and exacerbated cerebral beta-amyloidosis in B6Tg2576 mice. Compared with age-matched non-transgenic littermates, B6Tg2576 mice developed significantly more diet-induced aortic atherosclerosis. Unexpectedly, normal diet-fed B6Tg2576 mice also developed fatty streak lesions (early atherosclerosis) in the aorta. The aortic atherosclerotic lesion area positively correlated with cerebral beta-amyloid deposits in B6Tg2576 mice on both atherogenic and normal diets. Furthermore, behavioral assessments demonstrated that B6Tg2576 mice fed an atherogenic diet had more spatial learning impairment than those fed a normal diet. Our results suggest that synergistic mechanisms may be involved in the pathogenesis of atherosclerosis and AD. These findings may have important implications in the prevention and treatment of cardiovascular diseases as well as AD.
高脂肪/高胆固醇饮食会加剧阿尔茨海默病(AD)小鼠模型中的β-淀粉样变性。然而,在这些模型中研究动脉粥样硬化与β-淀粉样变性之间的关系一直是不可能的,因为此类小鼠具有抗动脉粥样硬化的遗传背景。在此,我们报告了易患动脉粥样硬化的AD模型小鼠B6Tg2576的建立。B6Tg2576小鼠是通过将Tg2576小鼠(一种过表达带有瑞典双突变体的人淀粉样β蛋白前体的AD小鼠模型)与C57BL/6小鼠(一种易患饮食诱导性动脉粥样硬化的品系)回交产生的。致动脉粥样硬化饮食在B6Tg2576小鼠中诱发了主动脉粥样硬化并加剧了脑β-淀粉样变性。与年龄匹配的非转基因同窝小鼠相比,B6Tg2576小鼠发生的饮食诱导性主动脉粥样硬化明显更多。出乎意料的是,正常饮食喂养的B6Tg2576小鼠主动脉中也出现了脂肪条纹病变(早期动脉粥样硬化)。在致动脉粥样硬化饮食和正常饮食条件下,B6Tg2576小鼠的主动脉粥样硬化病变面积与脑β-淀粉样沉积物呈正相关。此外,行为评估表明,喂食致动脉粥样硬化饮食的B6Tg2576小鼠比喂食正常饮食的小鼠有更严重的空间学习障碍。我们的结果表明,协同机制可能参与了动脉粥样硬化和AD的发病过程。这些发现可能对心血管疾病以及AD的预防和治疗具有重要意义。