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过氧化物酶体增殖物激活受体γ(PPARγ)配体对胰岛素抵抗状态下脂肪组织的影响。

The effect of PPARgamma ligands on the adipose tissue in insulin resistance.

作者信息

Hammarstedt A, Andersson C X, Rotter Sopasakis V, Smith U

机构信息

The Lundberg Laboratory for Diabetes Research, Department of Internal Medicine, Sahlgrenska University Hospital, SE-413 45, Göteborg, Sweden.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2005 Jul;73(1):65-75. doi: 10.1016/j.plefa.2005.04.008.

Abstract

Insulin resistance is frequently accompanied by obesity and both obesity and type 2 diabetes are associated with a mild chronic inflammation. Elevated levels of various cytokines, such as TNF-alpha and IL-6, are typically found in the adipose tissue in these conditions. It has been suggested that many cytokines produced in the adipose tissue are derived from infiltrated inflammatory cells. However, the adipose tissue itself has proven to be an important endocrine organ, secreting several hormones and cytokines, usually referred to as adipokines. Peroxisome proliferator-activated receptor (PPAR)gamma is essential for adipocyte proliferation and differentiation. In recent years, PPARgamma and its ligands, the thiazolidinediones (TZD), have achieved great attention due to their insulin sensitizing and anti-inflammatory properties. Treatment with TZDs result in improved insulin signaling and adipocyte differentiation, increased adipose tissue influx of free fatty acids and inhibition of cytokine expression and action. As a result, PPARgamma plays a central role in maintaining a functional and differentiated adipose tissue.

摘要

胰岛素抵抗常常伴有肥胖,而肥胖和2型糖尿病都与轻度慢性炎症相关。在这些情况下,通常会在脂肪组织中发现各种细胞因子水平升高,如肿瘤坏死因子-α和白细胞介素-6。有人提出,脂肪组织中产生的许多细胞因子都来源于浸润的炎症细胞。然而,脂肪组织本身已被证明是一个重要的内分泌器官,可分泌多种激素和细胞因子,通常称为脂肪因子。过氧化物酶体增殖物激活受体(PPAR)γ对脂肪细胞的增殖和分化至关重要。近年来,PPARγ及其配体噻唑烷二酮类药物(TZD)因其胰岛素增敏和抗炎特性而备受关注。使用TZD治疗可改善胰岛素信号传导和脂肪细胞分化,增加脂肪组织中游离脂肪酸的流入,并抑制细胞因子的表达和作用。因此,PPARγ在维持功能性和分化性脂肪组织中起着核心作用。

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