Animal models to study bile acid metabolism

被引:217
作者
Li, Jianing [1 ]
Dawson, Paul A. [1 ]
机构
[1] Emory Univ, Dept Pediat, Div Gastroenterol Hepatol & Nutr, Atlanta, GA 30322 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2019年 / 1865卷 / 05期
基金
美国国家卫生研究院;
关键词
Liver; Intestine; Enterohepatic circulation; Mouse model; Enzyme; Transporter; FARNESOID X RECEPTOR; FAMILIAL INTRAHEPATIC CHOLESTASIS; ANION-TRANSPORTING POLYPEPTIDES; BETA-MURICHOLIC ACID; ALPHA-OST-BETA; OXYSTEROL 7-ALPHA-HYDROXYLASE GENE; INTESTINAL CHOLESTEROL ABSORPTION; BILIARY LIPID SECRETION; INDUCED LIVER-INJURY; MDR2; P-GLYCOPROTEIN;
D O I
10.1016/j.bbadis.2018.05.011
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
The use of animal models, particularly genetically modified mice, continues to play a critical role in studying the relationship between bile acid metabolism and human liver disease. Over the past 20 years, these studies have been instrumental in elucidating the major pathways responsible for bile acid biosynthesis and enterohepatic cycling, and the molecular mechanisms regulating those pathways. This work also revealed bile acid differences between species, particularly in the composition, physicochemical properties, and signaling potential of the bile acid pool. These species differences may limit the ability to translate findings regarding bile acid-related disease processes from mice to humans. In this review, we focus primarily on mouse models and also briefly discuss dietary or surgical models commonly used to study the basic mechanisms underlying bile acid metabolism. Important phenotypic species differences in bile acid metabolism between mice and humans are highlighted.
引用
收藏
页码:895 / 911
页数:17
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