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胆汁酸代谢与信号转导。

Bile acid metabolism and signaling.

机构信息

Northeast Ohio Medical University, Rootstown, Ohio, USA.

出版信息

Compr Physiol. 2013 Jul;3(3):1191-212. doi: 10.1002/cphy.c120023.

Abstract

Bile acids are important physiological agents for intestinal nutrient absorption and biliary secretion of lipids, toxic metabolites, and xenobiotics. Bile acids also are signaling molecules and metabolic regulators that activate nuclear receptors and G protein-coupled receptor (GPCR) signaling to regulate hepatic lipid, glucose, and energy homeostasis and maintain metabolic homeostasis. Conversion of cholesterol to bile acids is critical for maintaining cholesterol homeostasis and preventing accumulation of cholesterol, triglycerides, and toxic metabolites, and injury in the liver and other organs. Enterohepatic circulation of bile acids from the liver to intestine and back to the liver plays a central role in nutrient absorption and distribution, and metabolic regulation and homeostasis. This physiological process is regulated by a complex membrane transport system in the liver and intestine regulated by nuclear receptors. Toxic bile acids may cause inflammation, apoptosis, and cell death. On the other hand, bile acid-activated nuclear and GPCR signaling protects against inflammation in liver, intestine, and macrophages. Disorders in bile acid metabolism cause cholestatic liver diseases, dyslipidemia, fatty liver diseases, cardiovascular diseases, and diabetes. Bile acids, bile acid derivatives, and bile acid sequestrants are therapeutic agents for treating chronic liver diseases, obesity, and diabetes in humans.

摘要

胆汁酸是肠道吸收营养物质和胆道分泌脂质、毒性代谢物和外源性物质的重要生理调节剂。胆汁酸也是信号分子和代谢调节剂,可激活核受体和 G 蛋白偶联受体 (GPCR) 信号通路,调节肝脏的脂质、葡萄糖和能量稳态,维持代谢稳态。胆固醇转化为胆汁酸对于维持胆固醇稳态、防止胆固醇、甘油三酯和毒性代谢物的蓄积以及肝脏和其他器官的损伤至关重要。胆汁酸在肝脏到肠道再回到肝脏的肠肝循环在营养物质吸收、分布以及代谢调节和稳态中发挥核心作用。这一生理过程受到肝脏和肠道中受核受体调节的复杂膜转运系统的调控。毒性胆汁酸可引起炎症、细胞凋亡和死亡。另一方面,胆汁酸激活的核受体和 GPCR 信号通路可防止肝脏、肠道和巨噬细胞中的炎症。胆汁酸代谢紊乱可导致胆汁淤积性肝病、血脂异常、脂肪肝、心血管疾病和糖尿病。胆汁酸、胆汁酸衍生物和胆汁酸螯合剂是治疗人类慢性肝病、肥胖症和糖尿病的治疗药物。

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本文引用的文献

2
The role of bile after Roux-en-Y gastric bypass in promoting weight loss and improving glycaemic control.
Endocrinology. 2012 Aug;153(8):3613-9. doi: 10.1210/en.2011-2145. Epub 2012 Jun 6.
3
Farnesoid X receptor targeting to treat nonalcoholic steatohepatitis.
Drug Discov Today. 2012 Sep;17(17-18):988-97. doi: 10.1016/j.drudis.2012.05.012. Epub 2012 May 29.
4
Bile acid receptors as targets for the treatment of dyslipidemia and cardiovascular disease.
J Lipid Res. 2012 Sep;53(9):1723-37. doi: 10.1194/jlr.R024794. Epub 2012 May 1.
5
Liver LXRα expression is crucial for whole body cholesterol homeostasis and reverse cholesterol transport in mice.
J Clin Invest. 2012 May;122(5):1688-99. doi: 10.1172/JCI59817. Epub 2012 Apr 9.
6
LXRα is uniquely required for maximal reverse cholesterol transport and atheroprotection in ApoE-deficient mice.
J Lipid Res. 2012 Jun;53(6):1126-33. doi: 10.1194/jlr.M022061. Epub 2012 Mar 26.
7
Transcriptional integration of metabolism by the nuclear sterol-activated receptors LXR and FXR.
Nat Rev Mol Cell Biol. 2012 Mar 14;13(4):213-24. doi: 10.1038/nrm3312.
8
Biliary and nonbiliary contributions to reverse cholesterol transport.
Curr Opin Lipidol. 2012 Apr;23(2):85-90. doi: 10.1097/MOL.0b013e3283508c21.
9
TGR5 activation inhibits atherosclerosis by reducing macrophage inflammation and lipid loading.
Cell Metab. 2011 Dec 7;14(6):747-57. doi: 10.1016/j.cmet.2011.11.006.
10
Glucose and insulin induction of bile acid synthesis: mechanisms and implication in diabetes and obesity.
J Biol Chem. 2012 Jan 13;287(3):1861-73. doi: 10.1074/jbc.M111.305789. Epub 2011 Dec 5.

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