A Triterpenoid Inhibited Hormone-Induced Adipocyte Differentiation and Alleviated Dexamethasone-Induced Insulin Resistance in 3T3-L1 adipocytes

被引:13
|
作者
Qin J.-H. [1 ]
Ma J.-Z. [2 ]
Yang X.-W. [2 ]
Hu Y.-J. [1 ]
Zhou J. [1 ]
Fu L.-C. [1 ]
Tian R.-H. [1 ]
Liu S. [1 ]
Xu G. [2 ]
Shen X.-L. [1 ]
机构
[1] Laboratory of Chinese Herbal Drug Discovery, Tropical Medicine Institute, Guangzhou University of Chinese Medicine, Guangzhou
[2] State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming
关键词
3T3-L1; 6α-Hydroxylup-20(29)-en-3-on-28-oic acid; Adipocyte differentiation; Adipocyte dysfunction; Dexamethasone-induced insulin resistance; PI3K/Akt2; signaling;
D O I
10.1007/s13659-015-0063-5
中图分类号
学科分类号
摘要
Abstract: 6α-Hydroxylup-20(29)-en-3-on-28-oic acid (1), a natural triterpenoid, was found to possess the ability in a dose-dependent manner inhibiting hormone-induced adipocyte differentiation in 3T3-L1 preadipocytes, and restoring glucose consuming ability in dexamethasone (DXM)-induced insulin resistant 3T3-L1 adipocytes. Compound 1 was also found to ameliorate DXM-induced adipocyte dysfunction in lipolysis and adipokine secretion. Mechanistic studies revealed that 1 inhibited adipocyte differentiation in 3T3-L1 preadipocytes via down-regulating hormone-stimulated gene transcription of peroxisome proliferator-activated receptor γ and CCAAT-enhancer-binding protein alpha which are key factors in lipogenesis, and restored DXM-impaired glucose consuming ability in differentiated 3T3-L1 adipocytes via repairing insulin signaling pathway and activating down-stream signaling transduction by phosphorylation of signaling molecules PI3K/p85, Akt2 and AS160, thus leading to increased translocation of glucose transporter type 4 and transportation of glucose. Graphical Abstract: [Figure not available: see fulltext.]. © 2015, The Author(s).
引用
收藏
页码:159 / 166
页数:7
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