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Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease.

Abstract
Bile acids are cholesterol-derived metabolites with a well-established role in the digestion and absorption of dietary fat. More recently, the discovery of bile acids as natural ligands for the nuclear farnesoid X receptor (FXR) and membrane Takeda G-protein-coupled receptor 5 (TGR5), and the recognition of the effects of FXR and TGR5 signaling have led to a paradigm shift in knowledge regarding bile acid physiology and metabolic health. Bile acids are now recognized as signaling molecules that orchestrate blood glucose, lipid and energy metabolism. Changes in FXR and/or TGR5 signaling modulates the secretion of gastrointestinal hormones including glucagon-like peptide-1 (GLP-1) and peptide YY (PYY), hepatic gluconeogenesis, glycogen synthesis, energy expenditure, and the composition of the gut microbiome. These effects may contribute to the metabolic benefits of bile acid sequestrants, metformin, and bariatric surgery. This review focuses on the role of bile acids in energy intake and body weight, particularly their effects on gastrointestinal hormone secretion, the changes in obesity and T2D, and their potential relevance to the management of metabolic disorders.
AuthorsCong Xie, Weikun Huang, Richard L Young, Karen L Jones, Michael Horowitz, Christopher K Rayner, Tongzhi Wu
JournalNutrients (Nutrients) Vol. 13 Issue 4 (Mar 28 2021) ISSN: 2072-6643 [Electronic] Switzerland
PMID33800566 (Publication Type: Journal Article, Review)
Chemical References
  • Bile Acids and Salts
  • Blood Glucose
  • Gastrointestinal Hormones
Topics
  • Bile Acids and Salts (metabolism)
  • Blood Glucose (metabolism)
  • Body Weight (drug effects)
  • Eating (drug effects)
  • Energy Metabolism (drug effects)
  • Gastrointestinal Hormones (metabolism)
  • Humans
  • Lipid Metabolism (drug effects)
  • Metabolic Diseases (metabolism)
  • Signal Transduction (drug effects)

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