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

Korean diabetes journal Pub Date : 2010-06-01 Epub Date: 2010-06-30 DOI:10.4093/kdj.2010.34.3.137
Jason K Kim
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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.

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炎症与胰岛素抵抗:一个有新想法的老故事。
早在胰岛素被发现之前,1901 年,抗炎药水杨酸钠就被用于治疗糖尿病。耐人寻味的是,在随后的许多年里,糖尿病一直被视为糖代谢紊乱,后来又被描述为脂质代谢失调的疾病。糖尿病研究的重点是肥胖与胰岛素抵抗之间的因果关系,胰岛素抵抗是 2 型糖尿病的主要特征。炎症是导致胰岛素抵抗的原因这一概念直到近 20 年才开始浮出水面。在肥胖症中,当巨噬细胞渗入脂肪组织并刺激脂肪细胞分泌炎症细胞因子时,炎症就会发生,进而影响能量平衡、葡萄糖和脂质代谢,导致胰岛素抵抗。本报告回顾了最近发现的涉及分子支架和内质网伴侣的应激激酶信号传导,这些信号传导可调节能量平衡和葡萄糖稳态。随着我们从概念理解到分子发现的不断进步,一个关于炎症和胰岛素抵抗的世纪故事又有了新的思路。
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