Liu Yang, Chang Yong-sheng, Fang Fu-de
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, CAMS and PUMC, Beijing 100005, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007 Jun;29(3):430-5.
Liver X receptors (LXRs) are members of the nuclear receptor superfamily and are activated by oxysterols and intermediates in the cholesterol synthetic pathway. The pivotal role of LXRs in the metabolic conversion of cholesterol to bile acids has been well established. Furthermore, insulin induces LXRa in hepatocytes, resulting in the suppression of key enzymes in gluconeogenesis, including phosphoenolpyruvate carboxykinase, glucose-6-phosphatase, and fructose-1, 6-bisphosphatase (FBPase). LXRs also play an important role in fatty acid metabolism by activating the sterol regulatory element-bing protein 1c gene (SREBP1c). This articles reviews the molecular mechanisms by which LXRs act to influence the lipid and carbohydrate metabolism.
肝脏X受体(LXRs)是核受体超家族的成员,可被氧化甾醇和胆固醇合成途径中的中间体激活。LXRs在胆固醇向胆汁酸的代谢转化中所起的关键作用已得到充分证实。此外,胰岛素可诱导肝细胞中的LXRα,从而抑制糖异生中的关键酶,包括磷酸烯醇式丙酮酸羧激酶、葡萄糖-6-磷酸酶和果糖-1,6-二磷酸酶(FBPase)。LXRs还通过激活固醇调节元件结合蛋白1c基因(SREBP1c)在脂肪酸代谢中发挥重要作用。本文综述了LXRs影响脂质和碳水化合物代谢的分子机制。