The bile acid membrane receptor TGR5: a valuable metabolic target
Open accessAbstract
Bile acids (BAs) are amphipathic molecules that facilitate the uptake of lipids, and their levels fluctuate in the intestines as well as in the circulation depending on food intake. Besides their role in dietary lipid absorption, BAs function as signaling molecules that activate specific BA receptors and trigger downstream signaling cascades. The BA receptors and the signaling pathways they control are not only important in the regulation of BA synthesis and their metabolism, but they also regulate glucose homeostasis, lipid metabolism and energy expenditure – processes relevant in the context of the metabolic syndrome. In addition to the function of the nuclear receptor FXRα in regulating local effects of BAs in the organs of the enterohepatic axis, increasing evidence points to a crucial role of the G-protein-coupled receptor TGR5 in mediating systemic actions of BAs. Here we review the current knowledge on BA receptors, with a strong focus on the cell membrane receptor TGR5, which has emerged as a promising target for intervention in metabolic diseases.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Bile acids activate TGR5 on intestinal L-cells, leading to GLP-1 secretion.
“Bile acids also activate the G-protein-coupled receptor TGR5 (also known as GPR131) located on intestinal L-cells, leading to GLP-1 secretion44.”
From Pathophysiology and treatment of type 2 diabetes: perspectives on the past, present, and future (2014) · cites this paper as [44]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 69 · Cited by 185
Research works printed but not linked: 1
- 24 Pierce KL, Premont RT, Lefkowitz RJ: Seventransmembrane receptors. Nat Rev Mol Cell Biol 2002; 3: 639-650.
- Authors
- Pols, T. W. H., Noriega, L. G., Nomura, M., Auwerx, J., & Schoonjans, K.
- Affiliations
- École Polytechnique Fédérale de Lausanne (CH)
- Venue
- Digestive Diseases
- Publisher
- S. Karger AG
- Published
- 2011
- Volume
- 29
- Issue
- 1
- Pages
- 37-44
- ISSN
- 0257-2753 (ISSN-L)
- 1421-9875
- PMC
- PMC3128138
- OpenAlex
- W1970059084
- Cited by
- 185
- References
- 69
- Citations by year
- 2026: 8 · 2025: 14 · 2024: 18 · 2023: 20 · 2022: 24 · 2021: 19 · 2020: 8 · 2019: 5 · 2018: 6 · 2017: 15 · 2016: 8 · 2015: 7 · 2014: 17 · 2013: 12 · 2012: 2
- FWCI
- 0.97
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Digestive Diseases (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Consejo Nacional de Ciencia y Tecnología
- National Institutes of Health
- 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
- TGR5, G protein-coupled receptors, bile acids, bile acid receptors, enterohepatic circulation, lipid metabolism, glucose homeostasis, energy expenditure, metabolic syndrome, therapeutic target
- MeSH terms
- Animals, Bile Acids and Salts, Cell Membrane, Humans, Metabolic Diseases, Signal Transduction, Receptors, G-Protein-Coupled
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review