Cited by 248Drug Transport and Resistance MechanismsCholesterol and Lipid MetabolismGut microbiota and health

The Role of Bile Acids in Glucose Metabolism and Their Relation with Diabetes

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Alberto González-Regueiro, José, Moreno-Castañeda, Lidia, Uribe, Misael, Carlos Chávez-Tapia, Norberto·2017·Annals of Hepatology

Abstract

Bile acids (BAs), the end products of cholesterol catabolism, are essential for the absorption of lipids and fat-soluble vitamins; but they have also emerged as novel signaling molecules that act as metabolic regulators. It has been well described that the enterohe-patic circulation, a nuclear (FXR) and a cytoplasmic (TGR5/M-BAR) receptor aid in controlling hepatic bile acid synthesis. Modulating bile acid synthesis greatly impacts in metabolism, because these receptors also are implicated in glucose, lipid, and energy expenditure. Recent studies had revealed the way these receptors participate in regulating gluconeogenesis, peripheral insulin sensitivity, glycogen synthesis, glucagon like peptide 1 (GLP-1) and insulin secretion. Nowadays, it is demonstrated that enhancing bile acid signaling in the intestine contributes to the metabolic benefits of bile acid sequestrants and bariatric surgery on glucose homeos-tasis. This paper discusses the role of bile acid as regulators of glucose metabolism and their potential as therapeutic targets for diabetes.

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  1. Sonne DP, Hansen M, Knop FK. Bile acid sequestrants in type 2 diabetes: potential effects of GLP-1 secretion. Eur J Endocrinol 2014; 171: R47-R65.

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Authors
Alberto González-Regueiro, J., Moreno-Castañeda, L., Uribe, M., & Carlos Chávez-Tapia, N.
Affiliations
Hospital Médica Sur (MX)
Venue
Annals of Hepatology
Publisher
Elsevier BV
Published
2017-11
Volume
16
Issue
Suppl. 1: s3-105.
Pages
S15-S20
ISSN
1665-2681 (ISSN-L)
OpenAlex
W3194266802
Cited by
247
References
49
Citations by year
2026: 25 · 2025: 26 · 2024: 43 · 2023: 34 · 2022: 34 · 2021: 38 · 2020: 20 · 2019: 12 · 2018: 15
FWCI
5.70
Type
journal article
Language
en
Open access
Locations
  • Annals of Hepatology (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Australian Government
Topics
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
  • Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Keywords
bile acids, glucose metabolism, diabetes mellitus, enterohepatic circulation, farnesoid X receptor, TGR5, bile acid synthesis, gluconeogenesis, insulin sensitivity, glycogen synthesis, glucagon-like peptide-1, insulin secretion, bile acid sequestrants, bariatric surgery, glucose homeostasis, therapeutic target
MeSH terms
Gastrointestinal Microbiome, Animals, Bacteria, Bile Acids and Salts, Energy Metabolism, Humans, Intestines, Obesity, Signal Transduction, Host-Pathogen Interactions, Dysbiosis

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