Supplementation of Saturated Long-Chain Fatty Acids Maintains Intestinal Eubiosis and Reduces Ethanol-induced Liver Injury in Mice
Open accessAbstract
Background & aims Alcoholic liver disease is a leading cause of mortality. Chronic alcohol consumption is accompanied by intestinal dysbiosis, and development of alcoholic liver disease requires gut-derived bacterial products. However, little is known about how alterations to the microbiome contribute to pathogenesis of alcoholic liver disease.Methods We used the Tsukamoto-French mouse model, which involves continuous intragastric feeding of isocaloric diet or alcohol for 3 weeks. Bacterial DNA from the cecum was extracted for deep metagenomic sequencing. Targeted metabolomics assessed concentrations of saturated fatty acids in cecal contents. To maintain intestinal metabolic homeostasis, diets of ethanol-fed and control mice were supplemented with saturated long-chain fatty acids (LCFA). Bacterial genes involved in fatty acid biosynthesis, amounts of lactobacilli, and saturated LCFA were measured in fecal samples of nonalcoholic individuals and patients with active alcohol abuse.Results Analyses of intestinal contents from mice revealed alcohol-associated changes to the intestinal metagenome and metabolome, characterized by reduced synthesis of saturated LCFA. Maintaining intestinal levels of saturated fatty acids in mice resulted in eubiosis, stabilized the intestinal gut barrier, and reduced ethanol-induced liver injury. Saturated LCFA are metabolized by commensal Lactobacillus and promote their growth. Proportions of bacterial genes involved in fatty acid biosynthesis were lower in feces from patients with active alcohol abuse than controls. Total levels of LCFA correlated with those of lactobacilli in fecal samples from patients with active alcohol abuse but not in controls.Conclusions In humans and mice, alcohol causes intestinal dysbiosis, reducing the capacity of the microbiome to synthesize saturated LCFA and the proportion of Lactobacillus species. Dietary approaches to restore levels of saturated fatty acids in the intestine might reduce ethanol-induced liver injury in patients with alcoholic liver disease.
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Mice receiving intragastric alcohol feeding show gut microbiota perturbations and reduced synthesis of long-chain fatty acids.
“Moreover, mice receiving intragastric alcohol feeding show perturbations of the intestinal microbiota, with reduced synthesis of long-chain fatty acids44.”
From The gut microbiome and liver cancer: mechanisms and clinical translation (2017) · cites this paper as [44]
In a mouse model of alcoholic liver disease, ethanol was found to inhibit biosynthesis of saturated fatty acids by the intestinal microflora.
“For example, in a mouse model of alcoholic liver disease, ethanol was found to inhibit biosynthesis of saturated fatty acids by the intestinal microflora.”
From Dietary lipids, gut microbiota and lipid metabolism (2019) · cites this paper as [18]
Dietary supplementation with saturated long-chain fatty acids, which were metabolized by and promoted growth of Lactobacillus, reversed alcohol-induced dysbiosis, stabilized the intestinal gut barrier, and reduced liver injury.
“Dietary supplementation with saturated long-chain fatty acids, which were metabolized by and promoted growth of Lactobacillus, reversed alcohol-induced dysbiosis, stabilized the intestinal gut barrier, and reduced liver injury [18].”
From Dietary lipids, gut microbiota and lipid metabolism (2019) · cites this paper as [18]
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References 59 · Cited by 322
- Authors
- Chen, P., Torralba, M., Tan, J., Embree, M., Zengler, K., Stärkel, P., van Pijkeren, J.-P., DePew, J., Loomba, R., Ho, S. B., Bajaj, J. S., Mutlu, E. A., Keshavarzian, A., Tsukamoto, H., Nelson, K. E., Fouts, D. E., & Schnabl, B.
- Affiliations
- University of California San Diego (US)
- J. Craig Venter Institute (US)
- UCLouvain (BE)
- Virginia Commonwealth University (US)
- Rush University Medical Center (US)
- University of Southern California (US)
- Corresponding author
- Schnabl, Bernd
- ORCID
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 148
- Issue
- 1
- Pages
- 203-214.e16
- ISSN
- 0016-5085 (ISSN-L)
- PMC
- PMC4274236
- OpenAlex
- W1983778185
- Cited by
- 322
- References
- 59
- Citations by year
- 2026: 15 · 2025: 16 · 2024: 21 · 2023: 26 · 2022: 40 · 2021: 35 · 2020: 27 · 2019: 27 · 2018: 30 · 2017: 31 · 2016: 28 · 2015: 22 · 2014: 3
- FWCI
- 11.49
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Libraries (submittedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (P50AA011999, DK097153)
- University of Michigan
- ABMRF/The Foundation for Alcohol Research
- National Institutes of Health (U01 AA021856, R01 AA020703, K08 DK081830)
- John A. Hartford Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Keywords
- alcoholic liver disease, ethanol-induced liver injury, gut dysbiosis, gut microbiota, dietary supplementation, Lactobacillus, fatty acid synthesis, intestinal barrier, gut-liver axis, alcohol abuse, cecal metabolome
- MeSH terms
- Ethanol, Animals, Bacteria, Disease Models, Animal, Fatty Acids, Feces, Intestinal Mucosa, Intestines, Lactobacillus, Liver Diseases, Alcoholic, Male, Mice, Inbred C57BL, Permeability, Time Factors, Bacterial Translocation, Dietary Supplements, Host-Pathogen Interactions, Metagenome, Metabolomics, Dysbiosis
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