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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).
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页码:159 / 166
页数:7
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