Role of bile acids in the regulation of the metabolic pathways
Open accessAbstract
Recent studies have revealed that bile acids (BAs) are not only facilitators of dietary lipid absorption but also important signaling molecules exerting multiple physiological functions. Some major signaling pathways involving the nuclear BAs receptor farnesoid X receptor and the G protein-coupled BAs receptor TGR5/M-BAR have been identified to be the targets of BAs. BAs regulate their own homeostasis via signaling pathways. BAs also affect diverse metabolic pathways including glucose metabolism, lipid metabolism and energy expenditure. This paper suggests the mechanism of controlling metabolism via BA signaling and demonstrates that BA signaling is an attractive therapeutic target of the metabolic syndrome.
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BSH is associated with regulation of energy balance and glucose metabolism.
“Moreover, BSH is associated with other beneficial functions including the regulation of energy balance and glucose metabolism [14].”
From Bile Salt Hydrolase Activity in the Food-Derived Strain Levilactobacillus brevis M3R3: Genomic and Functional Characterization (2026) · cites this paper as [14]
The Gastrointestinal Tract section (page unavailable) links microbial bile-acid deconjugation to changes in bile-acid signaling and glucose metabolism; the Energy Metabolism section links bile acids to energy expenditure. But the passages do not identify BSH or establish that BSH itself regulates either outcome. (LLM, conf=0.78)
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Self-citation
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Sorted by citations
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“Moreover, BSH is associated with other beneficial functions including the regulation of energy balance and glucose metabolism [14].”
- Authors
- Taoka, H., Yokoyama, Y., Morimoto, K., Kitamura, N., Tanigaki, T., Takashina, Y., Tsubota, K., & Watanabe, M.
- Affiliations
- Keio University (JP)
- Venue
- World Journal of Diabetes
- Publisher
- Baishideng Publishing Group Inc.
- Published
- 2016
- Volume
- 7
- Issue
- 13
- Pages
- 260
- ISSN
- 1948-9358 (ISSN-L)
- PMC
- PMC4937164
- OpenAlex
- W2471416206
- Cited by
- 80
- References
- 102
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 3 · 2023: 4 · 2022: 10 · 2021: 12 · 2020: 4 · 2019: 7 · 2018: 7 · 2017: 11 · 2016: 2
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by-nc
- Locations
- World Journal of Diabetes (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Health Sciences › Medicine › Pharmacology › Berberine and alkaloids research
- Keywords
- bile acids, bile acid signaling, farnesoid X receptor, TGR5, G protein-coupled receptors, nuclear receptors, bile acid homeostasis, glucose metabolism, lipid metabolism, energy expenditure, metabolic syndrome, therapeutic target
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.
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