Bourgoin Frédéric, Bachelard Hélène, Badeau Mylène, Mélançon Sébastien, Pitre Maryse, Larivière Richard, Nadeau André
Department of Medicine and Lipid Research Unit, Centre Hospitalier Université Laval (CHUL) Research Center,Quebec, Canada.
Am J Physiol Heart Circ Physiol. 2008 Sep;295(3):H1044-H1055. doi: 10.1152/ajpheart.00516.2008. Epub 2008 Jul 3.
This study was designed to examine the effects of a high-fat, high-sucrose (HFHS) diet on vascular and metabolic actions of insulin. Male rats were randomized to receive an HFHS or regular chow diet for 4 wk. In a first series of experiments, the rats had pulsed Doppler flow probes and intravascular catheters implanted to measure blood pressure, heart rate, and regional blood flows. Insulin sensitivity and vascular responses to insulin were assessed during a euglycemic hyperinsulinemic clamp performed in conscious rats. In a second series of experiments, new groups of rats were used to examine skeletal muscle glucose transport activity and to determine in vitro vascular reactivity, endothelial nitric oxide synthase (eNOS) protein expression in muscle and vascular tissues and endothelin content, nitrotyrosine formation, and NAD(P)H oxidase protein expression in vascular tissues. The HFHS-fed rats displayed insulin resistance, hyperinsulinemia, hypertriglyceridemia, hyperlipidemia, elevated blood pressure, and impaired insulin-mediated renal and skeletal muscle vasodilator responses. A reduction in endothelium-dependent vasorelaxation, accompanied by a decreased eNOS protein expression in muscles and blood vessel endothelium, and increased vascular endothelin-1 protein content were also noted in HFHS-fed rats compared with control rats. Furthermore, the HFHS diet induced a reduced insulin-stimulated glucose transport activity in muscles and increased levels of NAD(P)H oxidase protein and nitrotyrosine formation in vascular tissues. These findings support the importance of eNOS protein in linking metabolic and vascular disease and indicate the ability of a Westernized diet to induce endothelial dysfunction and to alter metabolic and vascular homeostasis.
本研究旨在探讨高脂高糖(HFHS)饮食对胰岛素血管及代谢作用的影响。雄性大鼠被随机分为两组,分别接受HFHS饮食或常规饲料喂养4周。在第一组实验中,给大鼠植入脉冲多普勒血流探头和血管内导管,以测量血压、心率和局部血流。在清醒大鼠进行的正常血糖高胰岛素钳夹实验中,评估胰岛素敏感性和血管对胰岛素的反应。在第二组实验中,使用新的大鼠组来检测骨骼肌葡萄糖转运活性,并测定体外血管反应性、肌肉和血管组织中内皮型一氧化氮合酶(eNOS)蛋白表达、内皮素含量、硝基酪氨酸形成以及血管组织中NAD(P)H氧化酶蛋白表达。喂养HFHS饮食的大鼠表现出胰岛素抵抗、高胰岛素血症、高甘油三酯血症、高脂血症、血压升高以及胰岛素介导的肾和骨骼肌血管舒张反应受损。与对照大鼠相比,喂养HFHS饮食的大鼠还出现内皮依赖性血管舒张功能降低,同时肌肉和血管内皮中eNOS蛋白表达减少,血管内皮素-1蛋白含量增加。此外,HFHS饮食导致肌肉中胰岛素刺激的葡萄糖转运活性降低,血管组织中NAD(P)H氧化酶蛋白水平和硝基酪氨酸形成增加。这些发现支持了eNOS蛋白在连接代谢性疾病和血管疾病中的重要性,并表明西式饮食能够诱导内皮功能障碍并改变代谢和血管内环境稳态。