首页> 美国卫生研究院文献>Diabetes >Resistance to High-Fat Diet–Induced Obesity but Exacerbated Insulin Resistance in Mice Overexpressing Preadipocyte Factor-1 (Pref-1)
【2h】

Resistance to High-Fat Diet–Induced Obesity but Exacerbated Insulin Resistance in Mice Overexpressing Preadipocyte Factor-1 (Pref-1)

机译:对高脂饮食诱导的肥胖的抵抗但过度表达前脂肪细胞因子1(Pref-1)的小鼠的胰岛素抵抗加剧

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>OBJECTIVE—White adipose tissue is a critical regulator of whole-body glucose metabolism. Preadipocyte factor-1 (Pref-1) is a secreted protein that inhibits adipocyte differentiation, both in vitro and in vivo. In this study, we have investigated the effects of Pref-1 overexpression on whole-body glucose homeostasis and its contribution to the development of insulin resistance.>RESEARCH DESIGN AND METHODS—To gain insight into the role of Pref-1 on the onset of insulin resistance and type 2 diabetes, we measured body composition and whole-body insulin-stimulated glucose metabolism during a hyperinsulinemic-euglycemic clamp in Pref-1 transgenic and wild-type control mice fed a high-fat diet.>RESULTS—Mice overexpressing Pref-1 were resistant to high-fat diet–induced obesity, as reflected by a marked reduction in adipose tissue mass. However, Pref-1–overexpressing mice were severely insulin resistant, mainly because of a reduction in insulin-stimulated glucose uptake in skeletal muscle and adipose tissue. The aggravated insulin resistance was associated with impaired insulin signaling and increased diacylglycerol content in skeletal muscle.>CONCLUSIONS—Mice overexpressing Pref-1 are insulin resistant despite being protected from diet-induced obesity and may provide a new rodent model for the study of lipodystrophic disorders.
机译:>目标— 白色脂肪组织是全身葡萄糖代谢的关键调节剂。 Preadipocyte factor-1(Pref-1)是一种分泌的蛋白质,在体内和体外均可抑制脂肪细胞的分化。在这项研究中,我们研究了Pref-1过表达对全身葡萄糖稳态的影响及其对胰岛素抵抗发展的贡献。>研究设计与方法— 以深入了解Pref-1的作用-1在胰岛素抵抗和2型糖尿病发作时,在高脂饮食的Pref-1转基因和野生型对照小鼠中,在高胰岛素-正常血糖钳夹期间测量了人体成分和全身胰岛素刺激的葡萄糖代谢。 >结果-过度表达Pref-1的小鼠对高脂饮食诱导的肥胖具有抵抗力,这可以通过脂肪组织量的明显减少来体现。但是,Pref-1过表达的小鼠对胰岛素的抵抗力很强,这主要是因为骨骼肌和脂肪组织中胰岛素刺激的葡萄糖摄取减少。胰岛素抵抗的加剧与胰岛素信号的减弱和骨骼肌中二酰基甘油含量的增加有关。>结论— 过度表达Pref-1的小鼠尽管不受饮食诱导的肥胖的影响,但仍具有胰岛素抵抗性,并可能提供一种新的啮齿动物模型用于研究脂肪营养障碍。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号