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首页> 外文期刊>Microvascular Research: An International Journal >Vascular dysfunction and impaired insulin signaling in high-fat diet fed ovariectomized mice.
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Vascular dysfunction and impaired insulin signaling in high-fat diet fed ovariectomized mice.

机译:高脂饮食去卵巢小鼠的血管功能障碍和胰岛素信号传导受损。

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The metabolic syndrome, characterized by conditions such as obesity and insulin resistance, is more prevalent in postmenopausal women than in premenopausal women, and increases the risk of cardiovascular disease and type 2 diabetes. The main objective of the present study was to investigate the combined effects of ovariectomy (OVX) and high-fat diet (HFD) on metabolic parameters, vascular function and glucose homeostasis in mice. After OVX or sham operation (Sham), mice were fed with either a normal diet (ND) or a HFD. Mice were divided into ND+Sham, ND+OVX, HFD+Sham, and HFD+OVX groups. After 4weeks, HFD+OVX mice developed marked increases in body weight and plasma insulin levels, but not blood glucose levels. The area under the glucose tolerance curve (Delta AUC(glucose)) following an oral glucose tolerance test and the homeostasis model assessment of insulin resistance (HOMA-IR) revealed that HFD+OVX mice had higher values than any other group. Concomitantly with these metabolic disturbances, decreased tail skin blood flow and augmented tail skin flushing, a marker of hot flashes, were observed in HFD+OVX mice. These vascular modulations likely result from vasomotor dysfunction. Furthermore, we investigated whether OVX and HFD affect the insulin signaling pathway in mice. Insulin-induced Akt phosphorylation in the livers of HFD+OVX mice was significantly downregulated compared with ND+Sham and HFD+Sham mice. Thus, the HFD+OVX mice used in the present study constitute an experimental animal model of postmenopausal metabolic syndrome. Herein, we provide experimental evidence that vascular dysfunction and impaired insulin signaling may contribute to the pathogenesis of postmenopausal metabolic syndrome.
机译:以肥胖和胰岛素抵抗等疾病为特征的代谢综合征在绝经后妇女中比在绝经前妇女中更为普遍,并增加了患心血管疾病和2型糖尿病的风险。本研究的主要目的是研究卵巢切除术(OVX)和高脂饮食(HFD)对小鼠代谢参数,血管功能和葡萄糖稳态的联合作用。在OVX或假手术(Sham)之后,给小鼠喂食正常饮食(ND)或HFD。将小鼠分为ND + Sham,ND + OVX,HFD + Sham和HFD + OVX组。 4周后,HFD + OVX小鼠的体重和血浆胰岛素水平显着升高,但血糖水平未升高。口服葡萄糖耐量试验和胰岛素抵抗稳态模型评估(HOMA-IR)后,葡萄糖耐量曲线下的面积(ΔAUC(葡萄糖))显示,HFD + OVX小鼠的值高于任何其他组。与这些代谢紊乱相伴的是,在HFD + OVX小鼠中观察到尾皮肤血流量减少和尾皮肤潮红增加,潮热是标志。这些血管调节可能是由血管舒缩功能障碍引起的。此外,我们调查了OVX和HFD是否会影响小鼠的胰岛素信号传导途径。与ND + Sham和HFD + Sham小鼠相比,HFD + OVX小鼠肝脏中胰岛素诱导的Akt磷酸化显着下调。因此,本研究中使用的HFD + OVX小鼠构成了绝经后代谢综合征的实验动物模型。在这里,我们提供实验证据,血管功能障碍和受损的胰岛素信号传导可能促成绝经后代谢综合征的发病机理。

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