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胰岛素抵抗及相关代谢紊乱中的神经鞘脂类和磷脂。

Sphingolipids and phospholipids in insulin resistance and related metabolic disorders.

机构信息

Baker IDI Heart and Diabetes Institute, 75 Commercial Road, Melbourne, 3004, Australia.

Department of Nutrition and Integrative Physiology, University of Utah, 201 Presidents Circle, Salt Lake City, Utah, 84112, USA.

出版信息

Nat Rev Endocrinol. 2017 Feb;13(2):79-91. doi: 10.1038/nrendo.2016.169. Epub 2016 Oct 21.

Abstract

Obesity, insulin resistance, type 2 diabetes mellitus and cardiovascular disease form a metabolic disease continuum that has seen a dramatic increase in prevalence in developed and developing countries over the past two decades. Dyslipidaemia resulting from hypercaloric diets is a major contributor to the pathogenesis of metabolic disease, and lipid-lowering therapies are the main therapeutic option for this group of disorders. However, the fact that dysfunctional lipid metabolism extends far beyond cholesterol and triglycerides is becoming increasingly clear. Lipidomic studies and mouse models are helping to explain the complex interactions between diet, lipid metabolism and metabolic disease. These studies are not only improving our understanding of this complex biology, but are also identifying potential therapeutic avenues to combat this growing epidemic. This Review examines what is currently known about phospholipid and sphingolipid metabolism in the setting of obesity and how metabolic pathways are being modulated for therapeutic effect.

摘要

肥胖症、胰岛素抵抗、2 型糖尿病和心血管疾病构成了一种代谢疾病连续统,在过去二十年中,这种连续统在发达国家和发展中国家的患病率显著增加。高卡路里饮食导致的血脂异常是代谢性疾病发病机制的主要原因,降脂治疗是治疗这组疾病的主要选择。然而,脂质代谢功能障碍远远超出胆固醇和甘油三酯的事实变得越来越明显。脂质组学研究和小鼠模型正在帮助解释饮食、脂质代谢和代谢性疾病之间的复杂相互作用。这些研究不仅提高了我们对这种复杂生物学的理解,而且还确定了潜在的治疗途径来对抗这一日益严重的流行。这篇综述探讨了目前已知的肥胖症背景下磷脂和鞘脂代谢情况,以及代谢途径如何被调节以产生治疗效果。

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