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Mechanism by Which Caloric Restriction Improves Insulin Sensitivity in Sedentary Obese Adults

机译:热量限制改善久坐肥胖成年人胰岛素敏感性的机制

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摘要

Caloric restriction (CR) improves insulin sensitivity and reduces the incidence of diabetes in obese individuals. The underlying mechanisms whereby CR improves insulin sensitivity are not clear. We evaluated the effect of 16 weeks of CR on whole-body insulin sensitivity by pancreatic clamp before and after CR in 11 obese participants (BMI = 35 kg/m~2) compared with 9 matched control subjects (BMI = 34 kg/m~2). Compared with the control subjects, CR increased the glucose infusion rate needed to maintain euglycemia during hyperinsuline-mia, indicating enhancement of peripheral insulin sensitivity. This improvement in insulin sensitivity was not accompanied by changes in skeletal muscle mitochon-drial oxidative capacity or oxidant emissions, nor were there changes in skeletal muscle ceramide, diacylglyc-erol, or amino acid metabolite levels. However, CR lowered insulin-stimulated thioredoxin-interacting protein (TXNIP) levels and enhanced nonoxidative glucose disposal. These results support a role for TXNIP in mediating the improvement in peripheral insulin sensitivity after CR.
机译:热量限制(CR)可改善胰岛素敏感性并降低肥胖个体中糖尿病的发生率。 CR改善胰岛素敏感性的潜在机制尚不清楚。我们评估了11个肥胖参与者(BMI = 35 kg / m〜2)与16个匹配对照组(BMI = 34 kg / m〜)相比,CR前后16周CR对胰腺全身胰岛素敏感性的影响。 2)。与对照组相比,CR增加了高胰岛素血症期间维持正常血糖所需的葡萄糖输注速率,表明外周胰岛素敏感性增强。胰岛素敏感性的这种改善不伴随骨骼肌线粒体-干细胞氧化能力或氧化剂排放的变化,也不伴随骨骼肌神经酰胺,二酰基甘油-芥子油或氨基酸代谢产物水平的变化。但是,CR降低了胰岛素刺激的硫氧还蛋白相互作用蛋白(TXNIP)的水平,并增强了非氧化性葡萄糖的处置。这些结果支持TXNIP在介导CR后外周胰岛素敏感性改善中的作用。

著录项

  • 来源
    《Diabetes》 |2016年第1期|74-84|共11页
  • 作者单位

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

    Howard Hughes Medical Institute and the Departments of Medicine and Cellular & Molecular Physiology, Yale University School of Medicine, New Haven, CT;

    Division of Endocrinology and Metabolism, Mayo Clinic College of Medicine, Rochester, MN;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:46:09

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