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2型糖尿病中的白色脂肪组织及抗糖尿病药物的作用

White adipose tissue in type 2 diabetes and the effect of antidiabetic drugs.

作者信息

Zhao Yixuan, Yue Rensong

机构信息

Chengdu University of Traditional Chinese Medicine, Hospital of Chengdu, University of Traditional Chinese Medicine, No. 39 Shi-er-qiao Road, Chengdu, Sichuan Province, 610072, P. R. China.

出版信息

Diabetol Metab Syndr. 2025 Apr 4;17(1):116. doi: 10.1186/s13098-025-01678-9.

DOI:10.1186/s13098-025-01678-9
PMID:40186308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11969724/
Abstract

White adipose tissue (WAT) is highly flexible and was previously considered a passive location for energy storage. Its endocrine function has been established for several years, earning it the title of an "endocrine organ" due to its ability to secrete many adipokines that regulate metabolism. WAT is one of the core tissues that influence insulin sensitivity. Its dysfunction enhances insulin resistance and type 2 diabetes (T2D) progression. However, T2D may cause WAT dysfunction, including changes in distribution, metabolism, adipocyte hypertrophy, inflammation, aging, and adipokines and free fatty acid levels, which may exacerbate insulin resistance. This review used PubMed to search WAT dysfunction in T2D and the effects of these changes on insulin resistance. Additionally, we described and discussed the effects of antidiabetic drugs, including insulin therapy, sulfonylureas, metformin, glucose-like peptide-1 receptor agonists, thiazolidinediones, and sodium-dependent glucose transporters-2 inhibitors, on WAT parameters under T2D conditions.

摘要

白色脂肪组织(WAT)具有高度的灵活性,以前被认为是能量储存的被动场所。其内分泌功能已被确立多年,因其能够分泌多种调节代谢的脂肪因子而被誉为“内分泌器官”。WAT是影响胰岛素敏感性的核心组织之一。其功能障碍会增强胰岛素抵抗并促进2型糖尿病(T2D)的进展。然而,T2D可能会导致WAT功能障碍,包括分布、代谢、脂肪细胞肥大、炎症、衰老以及脂肪因子和游离脂肪酸水平的变化,这可能会加剧胰岛素抵抗。本综述利用PubMed搜索T2D中的WAT功能障碍以及这些变化对胰岛素抵抗的影响。此外,我们描述并讨论了抗糖尿病药物,包括胰岛素治疗、磺脲类药物、二甲双胍、胰高血糖素样肽-1受体激动剂、噻唑烷二酮类药物和钠-葡萄糖协同转运蛋白-2抑制剂,在T2D条件下对WAT参数的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea36/11969724/0eb876a0caa7/13098_2025_1678_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea36/11969724/bc76f7a8c0a5/13098_2025_1678_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea36/11969724/0eb876a0caa7/13098_2025_1678_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea36/11969724/bc76f7a8c0a5/13098_2025_1678_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea36/11969724/0eb876a0caa7/13098_2025_1678_Fig2_HTML.jpg

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Enhancing insulin sensitivity in type 2 diabetes mellitus using apelin-loaded small extracellular vesicles from Wharton's jelly-derived mesenchymal stem cells: a novel therapeutic approach.利用来自脐带华通氏胶间充质干细胞的载脂联素小细胞外囊泡增强2型糖尿病患者的胰岛素敏感性:一种新型治疗方法。
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No evidence of compensatory changes in energy balance, despite reductions in body weight and liver fat, during dapagliflozin treatment in type 2 diabetes mellitus: A randomized, double-blind, placebo-controlled, cross-over trial (ENERGIZE).在 2 型糖尿病患者中,达格列净治疗可降低体重和肝脂肪,但没有证据表明能量平衡有代偿性变化:一项随机、双盲、安慰剂对照、交叉试验(ENERGIZE)。
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