Colonic Absorption of Low-Molecular-Weight Metabolites Influenced by the Intestinal Microbiome: A Pilot Study
Open accessAbstract
Low-molecular-weight metabolites produced by the intestinal microbiome play a direct role in health and disease. However, little is known about the ability of the colon to absorb these metabolites. It is also unclear whether these metabolites are bioavailable. Here, metabolomics techniques (capillary electrophoresis with time-of-flight mass spectrometry, CE-TOFMS), germ-free (GF) mice, and colonized (Ex-GF) mice were used to identify the colonic luminal metabolites transported to colonic tissue and/or blood. We focused on the differences in each metabolite between GF and Ex-GF mice to determine the identities of metabolites that are transported to the colon and/or blood. CE-TOFMS identified 170, 246, 166, and 193 metabolites in the colonic feces, colonic tissue, portal plasma, and cardiac plasma, respectively. We classified the metabolites according to the following influencing factors: (i) the membrane transport system of the colonocytes, (ii) metabolism during transcellular transport, and (iii) hepatic metabolism based on the similarity in the ratio of each metabolite between GF and Ex-GF mice and found 62 and 22 metabolites that appeared to be absorbed from the colonic lumen to colonocytes and blood, respectively. For example, 11 basic amino acids were transported to the systemic circulation from the colonic lumen. Furthermore, many low-molecular-weight metabolites influenced by the intestinal microbiome are bioavailable. The present study is the first to report the transportation of metabolites from the colonic lumen to colonocytes and somatic blood in vivo, and the present findings are critical for clarifying host-intestinal bacterial interactions.
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The presence of both 5AV and taurine in the mouse colon depends on the microbiota.
“The presence of both 5AV and taurine in the mouse colon depends on the microbiota (Figure S6A–B) (Matsumoto et al., 2017).”
From Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice (2019) · cites this paper as Matsumoto et al., 2017
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References 35 · Cited by 80
Research works printed but not linked: 1
- [34]MLT style. Press Release: The 1997 Nobel Prize in Chemistry".: Nobelprize.org. Nobel Media AB 2014; [19 May 2015]. Available from: < http://www.nobelprize.org/nobel_prizes/chemistry/laureates/1997/press.html>
- Authors
- Matsumoto, M., Ooga, T., Kibe, R., Aiba, Y., Koga, Y., & Benno, Y.
- Affiliations
- RIKEN (JP)
- Human Metabolome Technologies, Inc. (Japan) (JP)
- Tokai University (JP)
- Corresponding author
- Matsumoto, Mitsuharu
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2017-01-25
- Volume
- 12
- Issue
- 1
- Pages
- e0169207
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC5266324
- OpenAlex
- W2580424203
- Cited by
- 80
- References
- 35
- Citations by year
- 2026: 6 · 2025: 8 · 2024: 8 · 2023: 13 · 2022: 9 · 2021: 11 · 2020: 7 · 2019: 7 · 2018: 10 · 2017: 1
- FWCI
- 2.79
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- The Programme for Promotion of Basic and Applied Researches for Innovations in Bio-oriented Industry by the Biooriented Technology Research Advancement Institution (BRAIN)
- Kyodo Milk Industry Co. Ltd.
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolomics and Mass Spectrometry Studies
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- colonic absorption, low molecular weight metabolites, gut microbiota, germ-free mice, bioavailability, colonic epithelial cells, transcellular transport, hepatic metabolism, basic amino acids, host-microbe interactions, fecal metabolites, portal plasma
- MeSH terms
- Gastrointestinal Microbiome, Animals, Colon, Feces, Germ-Free Life, Mice, Inbred BALB C, Pilot Projects, Mass Spectrometry, Electrophoresis, Capillary, Mice, Metabolomics
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