Bile acids, obesity, and the metabolic syndrome

被引:214
作者
Ma, Huijuan [1 ]
Patti, Mary Elizabeth [2 ,3 ]
机构
[1] Hebei Gen Hosp, Dept Endocrinol & Metab, Shijiazhuang 050051, Hebei, Peoples R China
[2] Joslin Diabet Ctr, Div Res, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Boston, MA 02215 USA
关键词
Bile acids; FXR; TGR5; Obesity; Insulin resistance; FARNESOID-X-RECEPTOR; Y GASTRIC BYPASS; PERIPHERAL INSULIN SENSITIVITY; IMPROVES GLUCOSE-HOMEOSTASIS; IMPROVED GLYCEMIC CONTROL; TYPE-2; DIABETES-MELLITUS; DIET-INDUCED OBESITY; WEIGHT-LOSS; CHOLESTEROL; 7-ALPHA-HYDROXYLASE; ENDOGENOUS TRIGLYCERIDE;
D O I
10.1016/j.bpg.2014.07.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Bile acids are increasingly recognized as key regulators of systemic metabolism. While bile acids have long been known to play important and direct roles in nutrient absorption, bile acids also serve as signalling molecules. Bile acid interactions with the nuclear hormone receptor farnesoid X receptor (FXR) and the membrane receptor G-protein-coupled bile acid receptor 5 (TGR5) can regulate incretin hormone and fibroblast growth factor 19 (FGF19) secretion, cholesterol metabolism, and systemic energy expenditure. Bile acid levels and distribution are altered in type 2 diabetes and increased following bariatric procedures, in parallel with reduced body weight and improved insulin sensitivity and glycaemic control. Thus, modulation of bile acid levels and signalling, using bile acid binding resins, TGR5 agonists, and FXR agonists, may serve as a potent therapeutic approach for the treatment of obesity, type 2 diabetes, and other components of the metabolic syndrome in humans. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:573 / 583
页数:11
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