Maxwell Andrew J, Niebauer Josef, Lin Patrick S, Tsao Philip S, Bernstein Daniel, Cooke John P
Division of Cardiovascular Medicine, Program in Vascular Medicine and Biology, Stanford University, Stanford, CA 94305-5246, USA.
Vasc Med. 2009 Aug;14(3):249-57. doi: 10.1177/1358863X08100040.
We previously reported an attenuation of both exercise hyperemia and measures of aerobic capacity in hypercholesterolemic mice. In this study, we expanded upon the previous findings by examining the temporal and quantitative relationship of hypercholesterolemia to aerobic and anaerobic capacity and by exploring several potential mechanisms of dysfunction. Eight-week-old wild type (n = 123) and apoE knockout (n = 79) C57BL/6J mice were divided into groups with distinct cholesterol levels by feeding with regular or high-fat diets. At various ages, the mice underwent treadmill ergospirometry. To explore mechanisms, aortic ring vasodilator function and nitrate (NO(x)) activity, urinary excretion of NO(x), running muscle microvascular density and citrate synthase activity, as well as myocardial mass and histologic evidence of ischemia were measured. At 8 weeks of age, all mice had similar measures of exercise capacity. All indices of aerobic exercise capacity progressively declined at 12 and 20 weeks of age in the hypercholesterolemic mice as cholesterol levels increased while indices of anaerobic capacity remained unaffected. Across the four cholesterol groups, the degree of aerobic dysfunction was related to serum cholesterol levels; a relationship that was maintained after correcting for confounding factors. Associated with the deterioration in exercise capacity was a decline in measures of nitric oxide-mediated vascular function while there was no evidence of aberrations in functional or oxidative capacities or in other components of transport capacity. In conclusion, aerobic exercise dysfunction is observed in murine models of genetic and diet-induced hypercholesterolemia and is associated with a reduction in vascular nitric oxide production.
我们之前报道过,高胆固醇血症小鼠的运动性充血和有氧能力指标均有所减弱。在本研究中,我们通过研究高胆固醇血症与有氧和无氧能力的时间及定量关系,并探索几种潜在的功能障碍机制,对之前的研究结果进行了拓展。将8周龄的野生型(n = 123)和载脂蛋白E基因敲除(n = 79)C57BL/6J小鼠通过喂食常规或高脂饮食分为不同胆固醇水平的组。在不同年龄,对小鼠进行跑步机运动肺量计测试。为探索机制,测量了主动脉环舒张功能和硝酸盐(NO(x))活性、NO(x)的尿排泄量、跑步肌肉微血管密度和柠檬酸合酶活性,以及心肌质量和缺血的组织学证据。在8周龄时,所有小鼠的运动能力指标相似。随着胆固醇水平升高,高胆固醇血症小鼠在12周和20周龄时有氧运动能力的所有指标逐渐下降,而无氧能力指标未受影响。在四个胆固醇组中,有氧功能障碍的程度与血清胆固醇水平相关;在校正混杂因素后,这种关系依然存在。与运动能力下降相关的是一氧化氮介导的血管功能指标下降,而在功能或氧化能力或运输能力的其他组成部分方面没有异常证据。总之,在遗传和饮食诱导的高胆固醇血症小鼠模型中观察到有氧运动功能障碍,且与血管一氧化氮生成减少有关。