Role of bile acids in metabolic control
Abstract
Bile acids are endocrine molecules that in addition to facilitating the absorption of fat-soluble nutrients regulate numerous metabolic processes, including glucose, lipid, and energy homeostasis. The signaling actions of bile acids are mediated through specific bile-acid-activated nuclear and membrane-bound receptors. These receptors are not only expressed by tissues within the enterohepatic circulation such as the liver and the intestine, but also in other organs where bile acids mediate their systemic actions. In this review, we discuss bile acid signaling and the interplay with the gut microbiota in the pathophysiology of obesity, type 2 diabetes, and non-alcoholic fatty liver disease, and the role of surgical and pharmacological interventions on bile acid profiles and metabolism.
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Conjugated bile acids can behave as signalling molecules regulating systemic endocrine functions including triglyceride, cholesterol, and possibly glucose homeostasis and have direct antimicrobial effects.
“Conjugated BA can behave as signalling molecules regulating systemic endocrine functions including triglyceride, cholesterol, and possibly glucose homeostasis and have direct antimicrobial effects.11,14”
From <i>Lactiplantibacillus plantarum</i> strains KABP011, KABP012, and KABP013 modulate bile acids and cholesterol metabolism in humans (2024) · cites this paper as [14]
Bile salt hydrolase activity could influence lipid metabolism and cholesterol levels in the host through the activation of specific signalling pathways.
“This activity could influence lipid metabolism and cholesterol levels in the host through the activation of specific signalling pathways.14,17”
From <i>Lactiplantibacillus plantarum</i> strains KABP011, KABP012, and KABP013 modulate bile acids and cholesterol metabolism in humans (2024) · cites this paper as [14]
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Bile acids as key modulators of the brain-Gut-Microbiota axis in alzheimer’s disease
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“Anthropometric measurements, blood pressure, serum lipid profile, and biochemical measurements were determined at baseline and at Days 7, 14, 21, and 28 (see Supplementary material online, Figure S1 ).”
BackgroundInfluentialToward Precision Weight-Loss Dietary Interventions: Findings from the POUNDS Lost Trial
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- Authors
- Molinaro, A., Wahlström, A., & Marschall, H.-U.
- Affiliations
- University of Gothenburg (SE)
- Corresponding author
- Marschall, Hanns-Ulrich
- Venue
- Trends in Endocrinology & Metabolism
- Publisher
- Elsevier BV
- Published
- 2018-01
- Volume
- 29
- Issue
- 1
- Pages
- 31-41
- ISSN
- 1043-2760 (ISSN-L)
- OpenAlex
- W2768863961
- Cited by
- 447
- References
- 76
- Citations by year
- 2026: 42 · 2025: 46 · 2024: 70 · 2023: 42 · 2022: 69 · 2021: 65 · 2020: 53 · 2019: 38 · 2018: 21
- FWCI
- 3.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Endocrinology and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- bile acids, bile acid signaling, nuclear receptors, cell surface receptors, enterohepatic circulation, gut microbiota, obesity, type 2 diabetes, non-alcoholic fatty liver disease, energy homeostasis, lipid homeostasis, glucose homeostasis, bariatric surgery
- MeSH terms
- Gastrointestinal Microbiome, Receptor, Farnesoid X-Activated, Animals, Bile Acids and Salts, Diabetes Mellitus, Type 2, Humans, Obesity, Receptors, Cytoplasmic and Nuclear, Receptors, G-Protein-Coupled, Non-alcoholic Fatty Liver Disease
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