Transport and biological activities of bile acids

被引:125
作者
Zwicker, Brittnee L. [1 ]
Agellon, Luis B. [1 ]
机构
[1] McGill Univ, Sch Dietet & Human Nutr, Ste Anne De Bellevue, PQ H9X 3V9, Canada
基金
加拿大创新基金会; 加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
Enterohepatic circulation; Fabp6; Gut microbiota; Metabolic syndromes; Transporters; LIPID-BINDING PROTEIN; FARNESOID-X-RECEPTOR; ALPHA-OST-BETA; 7-ALPHA-HYDROXYLASE GENE CYP7A1; ENDOPLASMIC-RETICULUM STRESS; ORGANIC SOLUTE TRANSPORTER; CHOLESTEROL; 7-ALPHA-HYDROXYLASE; NUCLEAR RECEPTOR; CHENODEOXYCHOLIC ACID; URSODEOXYCHOLIC ACID;
D O I
10.1016/j.biocel.2013.04.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bile acids have emerged as important biological molecules that support the solubilization of various lipids and lipid-soluble compounds in the gut, and the regulation of gene expression and cellular function. Bile acids are synthesized from cholesterol in the liver and eventually released into the small intestine. The majority of bile acids are recovered in the distal end of the small intestine and then returned to the liver for reuse. The components of the mechanism responsible for the recycling of bile acids within the enterohepatic circulation have been identified whereas the mechanism for intracellular transport is less understood. Recently, the ileal lipid binding protein (ILBP; human gene symbol FABP6) was shown to be needed for the efficient transport of bile acids from the apical side to the basolateral side of enterocytes in the distal intestine. This review presents an overview of the transport of bile acids between the liver and the gut as well as within hepatocytes and enterocytes. A variety of pathologies is associated with the malfunction of the bile acid transport system. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1389 / 1398
页数:10
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