Cargando…

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

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 recogn...

Descripción completa

Detalles Bibliográficos
Autores principales: Xie, Cong, Huang, Weikun, Young, Richard L., Jones, Karen L., Horowitz, Michael, Rayner, Christopher K., Wu, Tongzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066182/
https://www.ncbi.nlm.nih.gov/pubmed/33800566
http://dx.doi.org/10.3390/nu13041104
_version_ 1783682514799296512
author Xie, Cong
Huang, Weikun
Young, Richard L.
Jones, Karen L.
Horowitz, Michael
Rayner, Christopher K.
Wu, Tongzhi
author_facet Xie, Cong
Huang, Weikun
Young, Richard L.
Jones, Karen L.
Horowitz, Michael
Rayner, Christopher K.
Wu, Tongzhi
author_sort Xie, Cong
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8066182
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-80661822021-04-25 Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease Xie, Cong Huang, Weikun Young, Richard L. Jones, Karen L. Horowitz, Michael Rayner, Christopher K. Wu, Tongzhi Nutrients Review 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. MDPI 2021-03-28 /pmc/articles/PMC8066182/ /pubmed/33800566 http://dx.doi.org/10.3390/nu13041104 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Review
Xie, Cong
Huang, Weikun
Young, Richard L.
Jones, Karen L.
Horowitz, Michael
Rayner, Christopher K.
Wu, Tongzhi
Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease
title Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease
title_full Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease
title_fullStr Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease
title_full_unstemmed Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease
title_short Role of Bile Acids in the Regulation of Food Intake, and Their Dysregulation in Metabolic Disease
title_sort role of bile acids in the regulation of food intake, and their dysregulation in metabolic disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066182/
https://www.ncbi.nlm.nih.gov/pubmed/33800566
http://dx.doi.org/10.3390/nu13041104
work_keys_str_mv AT xiecong roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease
AT huangweikun roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease
AT youngrichardl roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease
AT joneskarenl roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease
AT horowitzmichael roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease
AT raynerchristopherk roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease
AT wutongzhi roleofbileacidsintheregulationoffoodintakeandtheirdysregulationinmetabolicdisease