Department of Medicine and Physiology, UC Irvine Diabetes Center, Center for Epigenetics and Metabolism, University of California at Irvine, Irvine, CA, USA.
Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Nat Rev Mol Cell Biol. 2018 Oct;19(10):654-672. doi: 10.1038/s41580-018-0044-8.
The cause of insulin resistance in obesity and type 2 diabetes mellitus (T2DM) is not limited to impaired insulin signalling but also involves the complex interplay of multiple metabolic pathways. The analysis of large data sets generated by metabolomics and lipidomics has shed new light on the roles of metabolites such as lipids, amino acids and bile acids in modulating insulin sensitivity. Metabolites can regulate insulin sensitivity directly by modulating components of the insulin signalling pathway, such as insulin receptor substrates (IRSs) and AKT, and indirectly by altering the flux of substrates through multiple metabolic pathways, including lipogenesis, lipid oxidation, protein synthesis and degradation and hepatic gluconeogenesis. Moreover, the post-translational modification of proteins by metabolites and lipids, including acetylation and palmitoylation, can alter protein function. Furthermore, the role of the microbiota in regulating substrate metabolism and insulin sensitivity is unfolding. In this Review, we discuss the emerging roles of metabolites in the pathogenesis of insulin resistance and T2DM. A comprehensive understanding of the metabolic adaptations involved in insulin resistance may enable the identification of novel targets for improving insulin sensitivity and preventing, and treating, T2DM.
肥胖和 2 型糖尿病(T2DM)患者胰岛素抵抗的原因不仅局限于胰岛素信号转导受损,还涉及多种代谢途径的复杂相互作用。代谢组学和脂质组学产生的大型数据集的分析揭示了代谢物(如脂质、氨基酸和胆汁酸)在调节胰岛素敏感性方面的作用。代谢物可以通过调节胰岛素信号通路的组成部分(如胰岛素受体底物(IRSs)和 AKT)直接调节胰岛素敏感性,也可以通过改变多种代谢途径的底物通量间接调节胰岛素敏感性,包括脂肪生成、脂质氧化、蛋白质合成和降解以及肝糖异生。此外,代谢物和脂质对蛋白质的翻译后修饰,包括乙酰化和棕榈酰化,可以改变蛋白质的功能。此外,微生物群在调节底物代谢和胰岛素敏感性方面的作用正在显现。在这篇综述中,我们讨论了代谢物在胰岛素抵抗和 T2DM 发病机制中的新作用。全面了解胰岛素抵抗所涉及的代谢适应性可能有助于确定提高胰岛素敏感性以及预防和治疗 T2DM 的新靶点。