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代谢、合成代谢和促有丝分裂胰岛素反应:胰岛素受体激活剂的组织特异性视角

Metabolic, anabolic, and mitogenic insulin responses: A tissue-specific perspective for insulin receptor activators.

作者信息

Bedinger Daniel H, Adams Sean H

机构信息

XOMA Corporation, Berkeley, CA, USA.

Arkansas Children's Nutrition Center and University of Arkansas for Medical Sciences, Department of Pediatrics, Little Rock, AR, USA.

出版信息

Mol Cell Endocrinol. 2015 Nov 5;415:143-56. doi: 10.1016/j.mce.2015.08.013. Epub 2015 Aug 12.

Abstract

Insulin acts as the major regulator of the fasting-to-fed metabolic transition by altering substrate metabolism, promoting energy storage, and helping activate protein synthesis. In addition to its glucoregulatory and other metabolic properties, insulin can also act as a growth factor. The metabolic and mitogenic responses to insulin are regulated by divergent post-receptor signaling mechanisms downstream from the activated insulin receptor (IR). However, the anabolic and growth-promoting properties of insulin require tissue-specific inter-relationships between the two pathways, and the nature and scope of insulin-regulated processes vary greatly across tissues. Understanding the nuances of this interplay between metabolic and growth-regulating properties of insulin would have important implications for development of novel insulin and IR modulator therapies that stimulate insulin receptor activation in both pathway- and tissue-specific manners. This review will provide a unique perspective focusing on the roles of "metabolic" and "mitogenic" actions of insulin signaling in various tissues, and how these networks should be considered when evaluating selective pharmacologic approaches to prevent or treat metabolic disease.

摘要

胰岛素通过改变底物代谢、促进能量储存以及帮助激活蛋白质合成,充当空腹到进食代谢转变的主要调节因子。除了其血糖调节和其他代谢特性外,胰岛素还可作为一种生长因子。对胰岛素的代谢和促有丝分裂反应由活化的胰岛素受体(IR)下游不同的受体后信号传导机制调节。然而,胰岛素的合成代谢和生长促进特性需要两条途径之间的组织特异性相互关系,并且胰岛素调节过程的性质和范围在不同组织中差异很大。了解胰岛素代谢和生长调节特性之间这种相互作用的细微差别,对于开发以途径和组织特异性方式刺激胰岛素受体激活的新型胰岛素和IR调节剂疗法具有重要意义。本综述将提供一个独特的视角,重点关注胰岛素信号在各种组织中的“代谢”和“促有丝分裂”作用,以及在评估预防或治疗代谢性疾病的选择性药理学方法时应如何考虑这些网络。

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