Duran-Sandoval Daniel, Cariou Bertrand, Fruchart Jean-Charles, Staels Bart
U.R.545 Inserm, Département d'Atherosclerosis, Institut Pasteur de Lille et Faculté de Pharmacie, Université de Lille 2, 1, rue du Professeur-Calmette, BP245, 59019 Lille, France.
Biochimie. 2005 Jan;87(1):93-8. doi: 10.1016/j.biochi.2004.11.018.
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.
血脂异常和胆囊疾病是目前在患有代谢综合征和2型糖尿病的患者中观察到的两种异常情况。胆汁酸激活的核受体法尼醇X受体(FXR)控制胆汁酸以及脂质代谢。最近的观察表明FXR在碳水化合物代谢中也发挥作用。在体内,糖尿病动物模型中肝脏FXR表达发生改变,并且在体外受激素和营养物质调节。在分子水平上,FXR激活会改变控制糖异生和脂肪生成的不同转录因子的转录活性,从而共同影响胆汁酸、脂质和碳水化合物代谢。本综述重点关注我们对FXR调节碳水化合物代谢的最新认识进展。这些观察结果引发了这种受体在代谢综合征中也具有调节作用的有趣可能性。