法尼甾体X受体
脂质代谢
胆汁酸
硼胆酸
背景(考古学)
新陈代谢
核受体
脂肪变性
化学
生物化学
受体
内科学
生物
内分泌学
医学
兴奋剂
转录因子
古生物学
基因
作者
Marleen Schonewille,Jan Freark de Boer,Albert K. Groen
出处
期刊:Current Opinion in Lipidology
[Ovid Technologies (Wolters Kluwer)]
日期:2016-04-19
卷期号:27 (3): 295-301
被引量:45
标识
DOI:10.1097/mol.0000000000000303
摘要
The view on bile salts has evolved over the years from being regarded as simple detergents that aid intestinal absorption of fat-soluble nutrients to being important hormone-like integrators of metabolism. This review provides an update on the rapidly developing field of interactions between bile salts and lipid metabolism, with a particular emphasis on the underlying mechanisms.The nuclear receptor farnesoid X receptor (FXR) plays major roles in bile salt-mediated signaling pathways. The recent identification of novel FXR targets and factors involved in FXR signaling highlights the interactions of bile acids with lipid metabolism. Exciting data have been reported on the use of intestine-specific FXR agonists as well as antagonists. In addition, encouraging results for treatment of hepatic steatosis obtained with obeticholic acid in the FLINT trial underline the therapeutic potential of bile salt signaling and metabolism for the treatment of lipid disorders.Modulation of FXR activity appears to be a potent target, not only for improving bile salt homeostasis, but also to improve lipid metabolism. Depending on the metabolic context both, FXR agonists as well as antagonists, could prove to be of therapeutic benefit.
科研通智能强力驱动
Strongly Powered by AbleSci AI