Hepatic insulin resistance ties cholesterol gallstone formation and the metabolic syndrome

被引:10
作者
Kovacs, Peter [2 ]
Kurtz, Ulrike [1 ]
Wittenburg, Henning [1 ]
机构
[1] Univ Leipzig, Dept Med 2, D-04103 Leipzig, Germany
[2] Univ Leipzig, Interdisciplinary Ctr Clin Res, D-04103 Leipzig, Germany
关键词
Diabetes mellitus type 2; cholelithiasis; cholesterol transport; ABCG5/ABCG8;
D O I
10.1016/S1665-2681(19)31861-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Despite the well-documented association between gallstones and the metabolic syndrome, 1,2 the mechanistic links between these two disorders remain unknown. Here we show that mice solely with hepatic insulin resistance, created by liver-specific disruption of the insulin receptor (LIRKO mice)(3) are markedly predisposed toward cholesterol gallstone formation due to at least two distinct mechanisms. Disinhibition of the forkhead transcription factor FoxO1, increases expression of the biliary cholesterol transporters Abcg5 and Abcg8, resulting in an increase in biliary cholesterol secretion. Hepatic insulin resistance also decreases expression of the bile acid synthetic enzymes, particularly Cyp7b1, and produces partial resistance to the farnesoid X receptor, leading to a lithogenic bile salt profile. As a result, after twelve weeks on a lithogenic diet, all of the LIRKO mice develop gallstones. Thus, hepatic insulin resistance provides a crucial link between the metabolic syndrome and increased cholesterol gallstone susceptibility.
引用
收藏
页码:262 / 264
页数:3
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