Roberts Christian K, Won Dean, Pruthi Sandeep, Kurtovic Silvia, Sindhu Ram K, Vaziri Nosratola D, Barnard R James
Department of Physiological Science, University of California, Los Angeles, CA 90095-1606, USA.
J Appl Physiol (1985). 2006 May;100(5):1657-65. doi: 10.1152/japplphysiol.01292.2005. Epub 2005 Dec 15.
The present study was designed to examine the effects of lifestyle modification on key contributing factors to atherogenesis, including oxidative stress, inflammation, chemotaxis, and cell adhesion. Obese men (n = 31), 15 of whom had metabolic syndrome, were placed on a high-fiber, low-fat diet in a 3-wk residential program where food was provided ad libitum and daily aerobic exercise was performed. In each subject, pre- and postintervention fasting blood was drawn for circulating levels of serum lipids, glucose and insulin (for estimation of insulin sensitivity), oxidative stress-generating enzyme myeloperoxidase and marker 8-isoprostaglandin F2alpha, the inflammatory protein C-reactive protein, soluble ICAM-1 as an indicator of endothelial activation, sP-selectin as a marker of platelet activation, the chemokine macrophage inflammatory protein-1alpha, and total matrix metalloproteinase-9. Using subject sera and human aortic endothelial cell culture systems, we measured VCAM-1 cell surface abundance and monocyte chemotactic protein-1, nitric oxide, superoxide, and hydrogen peroxide production in vitro by fluorometric detection. Also determined in vitro was serum-induced, monocyte adhesion and monocyte chemotactic activity. After 3 wk, significant reductions (P < 0.05) in body mass index, all serum lipids and lipid ratios, fasting glucose, insulin, homeostasis model assessment for insulin resistance, myeloperoxidase, 8-isoprostaglandin F2alpha, C-reactive protein, soluble ICAM-1, soluble P-selectin, macrophage inflammatory protein-1alpha, and matrix metalloproteinase-9 were noted. In vitro, serum-stimulated cellular VCAM-1 expression, monocyte chemotactic protein-1 production, and fluorometric detection of superoxide and hydrogen peroxide production decreased, whereas a concomitant increase in NO production was noted (all P < 0.01). Additionally, both monocyte adhesion (P < 0.05) and MCA (P < 0.01) decreased. Nine of 15 were no longer positive for metabolic syndrome postintervention. Intensive lifestyle modification may ameliorate novel coronary artery disease risk factors in men with metabolic syndrome factors before reversal of obesity.
本研究旨在探讨生活方式改变对动脉粥样硬化形成的关键促成因素的影响,包括氧化应激、炎症、趋化作用和细胞黏附。31名肥胖男性(其中15人患有代谢综合征)参加了一项为期3周的住院项目,采用高纤维、低脂饮食,食物可随意食用,并进行每日有氧运动。采集每位受试者干预前后的空腹血样,检测血清脂质、葡萄糖和胰岛素的循环水平(用于评估胰岛素敏感性)、氧化应激产生酶髓过氧化物酶和标志物8-异前列腺素F2α、炎症蛋白C反应蛋白、可溶性细胞间黏附分子-1(作为内皮激活的指标)、可溶性P选择素(作为血小板激活的标志物)、趋化因子巨噬细胞炎性蛋白-1α和总基质金属蛋白酶-9。利用受试者血清和人主动脉内皮细胞培养系统,通过荧光检测法在体外测量血管细胞黏附分子-1(VCAM-1)细胞表面丰度、单核细胞趋化蛋白-1、一氧化氮、超氧化物和过氧化氢的产生。还在体外测定了血清诱导的单核细胞黏附和单核细胞趋化活性。3周后,体重指数、所有血清脂质和脂质比率、空腹血糖、胰岛素、胰岛素抵抗的稳态模型评估、髓过氧化物酶、8-异前列腺素F2α、C反应蛋白、可溶性细胞间黏附分子-1、可溶性P选择素、巨噬细胞炎性蛋白-1α和基质金属蛋白酶-9均显著降低(P<0.05)。在体外,血清刺激的细胞VCAM-1表达、单核细胞趋化蛋白-1产生以及超氧化物和过氧化氢产生的荧光检测均降低,而一氧化氮产生则相应增加(均P<0.01)。此外,单核细胞黏附(P<0.05)和单核细胞趋化活性(P<0.01)均降低。15名受试者中有9人在干预后代谢综合征不再呈阳性。强化生活方式改变可能在肥胖逆转之前改善患有代谢综合征因素的男性的新型冠状动脉疾病风险因素。