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Amorfrutins are potent antidiabetic dietary natural products

机译:Amorfrutins是有效的抗糖尿病饮食天然产品

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摘要

Given worldwide increases in the incidence of obesity and type 2 diabetes, new strategies for preventing and treating metabolic diseases are needed. The nuclear receptor PPARy (peroxisome pro-liferator-activated receptor gamma) plays a central role in lipid and glucose metabolism; however, current PPARγ-targeting drugs are characterized by undesirable side effects. Natural products from edible biomaterial provide a structurally diverse resource to alleviate complex disorders via tailored nutritional intervention. We identified a family of natural products, the amorfrutins, from edible parts of two legumes, Glycyrrhiza foetida and Amorpha fruticosa, as structurally new and powerful antidiabetics with unprecedented effects for a dietary molecule. Amorfrutins bind to and activate PPARγ, which results in selective gene expression and physiological profiles markedly different from activation by current synthetic PPARγ drugs. In diet-induced obese and db/db mice, amorfrutin treatment strongly improves insulin resistance and other metabolic and inflammatory parameters without concomitant increase of fat storage or other unwanted side effects such as hepatoxicity. These results show that selective PPARy-activation by diet-derived ligands may constitute a promising approach to combat metabolic disease.
机译:鉴于全世界肥胖症和2型糖尿病的发病率上升,需要预防和治疗代谢性疾病的新策略。核受体PPARγ(过氧化物酶体增殖物激活受体γ)在脂质和葡萄糖代谢中起着核心作用。然而,目前的靶向PPARγ的药物具有不良副作用的特征。来自可食用生物材料的天然产品提供了结构多样的资源,可通过量身定制的营养干预措施来缓解复杂疾病。我们从两种豆科植物的甘草和甘草中的可食用部分中鉴定出了一种天然产品,即阿莫frutins,是一种结构新颖而功能强大的抗糖尿病药,对饮食分子具有空前的作用。 Amorfrutins结合并激活PPARγ,这导致选择性基因表达和生理特征与当前合成PPARγ药物的激活显着不同。在饮食诱发的肥胖和db / db小鼠中,阿莫frutin治疗可显着改善胰岛素抵抗以及其他代谢和炎症参数,而不会同时增加脂肪储存或其他不良副作用,例如肝毒性。这些结果表明,饮食来源的配体对PPARγ的选择性激活可能构成对抗代谢性疾病的一种有前途的方法。

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  • 作者单位

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany,Department of Biology, Chemistry, and Pharmacy, Free University of Berlin, Takustrasse 3, 14195 Berlin, Germany;

    Division of Structural Biology, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124 Braunschweig, Germany;

    Department of Chemistry and Chemical Biology and Boyce Thompson Institute, Cornell University, Ithaca, NY 14853;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

    Lead Discovery Center GmbH, Emil-Figge-Strasse 76a, 44227 Dortmund, Germany;

    Lead Discovery Center GmbH, Emil-Figge-Strasse 76a, 44227 Dortmund, Germany;

    Lead Discovery Center GmbH, Emil-Figge-Strasse 76a, 44227 Dortmund, Germany;

    AnalytiCon Discovery GmbH, Hermannswerder Haus 17, 14473 Potsdam, Germany;

    AnalytiCon Discovery GmbH, Hermannswerder Haus 17, 14473 Potsdam, Germany;

    German Institute of Human Nutrition, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany;

    German Institute of Human Nutrition, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany;

    German Institute of Human Nutrition, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany;

    Department of Chemistry and Chemical Biology and Boyce Thompson Institute, Cornell University, Ithaca, NY 14853;

    Division of Structural Biology, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124 Braunschweig, Germany;

    Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany;

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

    nuclear receptors; nutrition; compound screening; organic synthesis; x-ray structure;

    机译:核受体营养;复合筛选;有机合成X射线结构;

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