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炎症与胰岛素抵抗:一个有新观点的老故事。

Inflammation and insulin resistance: an old story with new ideas.

作者信息

Kim Jason K

机构信息

Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

出版信息

Korean Diabetes J. 2010 Jun;34(3):137-45. doi: 10.4093/kdj.2010.34.3.137. Epub 2010 Jun 30.

Abstract

Years before insulin was discovered, anti-inflammatory sodium salicylate was used to treat diabetes in 1901. Intriguingly for many years that followed, diabetes was viewed as a disorder of glucose metabolism, and then it was described as a disease of dysregulated lipid metabolism. The diabetes research focused on the causal relationship between obesity and insulin resistance, a major characteristic of type 2 diabetes. It is only within the past 20 years when the notion of inflammation as a cause of insulin resistance began to surface. In obesity, inflammation develops when macrophages infiltrate adipose tissue and stimulate adipocyte secretion of inflammatory cytokines, that in turn affect energy balance, glucose and lipid metabolism, leading to insulin resistance. This report reviews recent discoveries of stress kinase signaling involving molecular scaffolds and endoplasmic reticulum chaperones that regulate energy balance and glucose homeostasis. As we advance from a conceptual understanding to molecular discoveries, a century-old story of inflammation and insulin resistance is re-born with new ideas.

摘要

在胰岛素被发现的多年前,抗炎药物水杨酸钠于1901年被用于治疗糖尿病。在随后的许多年里,有趣的是,糖尿病先是被视为一种葡萄糖代谢紊乱疾病,之后又被描述为脂质代谢失调的疾病。糖尿病研究聚焦于肥胖与胰岛素抵抗之间的因果关系,胰岛素抵抗是2型糖尿病的一个主要特征。直到过去20年,炎症作为胰岛素抵抗病因的概念才开始浮现。在肥胖状态下,当巨噬细胞浸润脂肪组织并刺激脂肪细胞分泌炎性细胞因子时,炎症就会发生,而这些炎性细胞因子反过来又会影响能量平衡、葡萄糖和脂质代谢,导致胰岛素抵抗。本报告回顾了应激激酶信号传导的最新发现,这些发现涉及调节能量平衡和葡萄糖稳态的分子支架和内质网伴侣蛋白。随着我们从概念性理解深入到分子层面的发现,一个有着百年历史的炎症与胰岛素抵抗的故事以新的观点再次兴起。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fda7/2898926/ed4cd26e3a9f/kdj-34-137-g001.jpg

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