Potential regulatory role of the farnesoid X receptor in the metabolic syndrome

被引:33
|
作者
Duran-Sandoval, D
Cariou, B
Fruchart, JC
Staels, B
机构
[1] Univ Lille 2, Inst Pasteur, INSERM, UR545,Dept Atherosclerosis, F-59019 Lille, France
[2] Univ Lille 2, Fac Pharm, F-59019 Lille, France
关键词
FXR; insulin resistance; SHP; gluconeogenesis; metabolic syndrome;
D O I
10.1016/j.biochi.2004.11.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dyslipidemia and gallbladder diseases are two current anomalies observed in patients suffering from the metabolic syndrome and type 2 diabetes. The bile acid-activated nuclear receptor farnesoid X receptor (FXR) controls bile acid as well as lipid metabolism. Recent observations indicate a role for FXR also in carbohydrate metabolism. Hepatic FXR expression is altered in diabetic animal models in vivo and regulated by hormones and nutrients in vitro. At the molecular level, FXR activation modifies the transcriptional activity of different transcription factors controlling gluconeogenesis and lipogenesis, thus affecting in concert bile acid, lipid and carbohydrate metabolism. The present review focuses on recent advances in our understanding of the modulation of carbohydrate metabolism by FXR. These observations raise the intriguing possibility for a modulatory role of this receptor also in the metabolic syndrome. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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