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Effects of diet-induced obesity on protein expression in insulin signaling pathways of skeletal muscle in male Wistar rats

机译:节食性肥胖对Wistar雄性大鼠骨骼肌胰岛素信号通路蛋白表达的影响

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Background: The prevalence of diet-induced obesity is increasing globally, and posing significant health problems for millions of people worldwide. Diet-induced obesity is a major contributor to the global pandemic of type 2 diabetes mellitus. The reduced ability of muscle tissue to regulate glucose homeostasis plays a major role in the development and prognosis of type 2 diabetes. In this study, an animal model of diet-induced obesity was used to elucidate changes in skeletal muscle insulin signaling in obesity-induced diabetes.Methods: Adult male Wistar rats were randomized and assigned to either a control group or to a test group. Controls were fed a standard laboratory pellet diet (chow-fed), while the test group had free access to a highly palatable diet (diet-fed). After 8 weeks, the diet-fed animals were subdivided into three subgroups and their diets were altered as follows: diet-to-chow, diet-fed with addition of fenofibrate given by oral gavage for a further 7 weeks, or diet-fed with vehicle given by oral gavage for a further 7 weeks, respectively.Results: Untreated diet-fed animals had a significantly higher body weight and metabolic profile than the control chow-fed animals. Intramuscular triacylglyceride levels in the untreated obese animals were significantly higher than those in the control chow-fed group. Expression of protein kinase C beta, phosphatidylinositol 3, Shc, insulin receptor substrate 1, ERK1/2, and endothelial nitric oxide synthase was significantly increased by dietary obesity, while that of insulin receptor beta, insulin receptor substrate 1, and protein kinase B (Akt) were not affected by obesity.Conclusion: These data suggest that diet-induced obesity affects insulin signaling mechanisms, leading to insulin resistance in muscle.
机译:背景:饮食引起的肥胖症在全球范围内呈上升趋势,并给全球数百万人构成严重的健康问题。饮食引起的肥胖是导致全球2型糖尿病大流行的主要因素。肌肉组织调节葡萄糖稳态的能力降低在2型糖尿病的发生和预后中起着重要作用。在这项研究中,使用饮食诱发的肥胖症动物模型阐明了肥胖症诱发的糖尿病患者骨骼肌胰岛素信号的变化。方法:成年雄性Wistar大鼠随机分为对照组或试验组。对照组接受标准的实验室颗粒饮食(全脂喂养),而测试组可以自由享用高度可口的饮食(饮食)。 8周后,将饮食喂养的动物细分为三个亚组,并按以下方式更改饮食:按饮食选择饮食,通过另外管饲法加用非诺贝特的饮食喂养另外7周或通过饮食控制的饮食喂养。结果:未经处理的饮食喂养的动物的体重和代谢状况明显高于对照食物喂养的动物。未经治疗的肥胖动物的肌内甘油三酯水平显着高于对照食物喂养的组。饮食肥胖会显着增加蛋白激酶Cβ,磷脂酰肌醇3,Shc,胰岛素受体底物1,ERK1 / 2和内皮型一氧化氮合酶的表达,而胰岛素受体β,胰岛素受体底物1和蛋白激酶B的表达(结论:这些数据表明饮食诱导的肥胖会影响胰岛素信号传导机制,从而导致肌肉中的胰岛素抵抗。

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