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Amorfrutins are potent antidiabetic dietary natural products

机译:amorfrutins是有效的抗糖尿病膳食天然产品

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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 PPARγ (peroxisome proliferator-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 PPARγ-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的受体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物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的疾病。我们从两个豆科植物甘草和紫穗槐的可食部分中鉴定出了一种天然产品,即阿莫frutins,它们是结构上强大的新型抗糖尿病药物,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疾病的一种有前途的方法。

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