The metabolism of14C-labelled trimethylamine and its N-oxide in man
Abstract
The metabolism and elimination of 14C-labelled trimethylamine and its N-oxide (100 mg orally) were studied in three male volunteers. For both compounds the urine was the major route of elimination, with 95% of the administered 14C being voided in the first 24 h. No radioactivity was found in expired air. The majority (greater than 95%) of the urinary 14C from both compounds was excreted as trimethylamine N-oxide.
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After radiolabeled TMA or TMAO is given to people, 94.5% of the dose label is excreted in urine within 24 h, 4% in feces, and less than 1% in breath.
“After administration of radiolabeled TMA or TMAO to people, 94.5% of the dose label was excreted in the urine within 24 h; only 4% of the dose was excreted in the feces and <1% in the breath (2).”
From Trimethylamine <i>N</i> -Oxide, the Microbiome, and Heart and Kidney Disease (2017) · cites this paper as [2]
When radiolabeled trimethylamine or trimethylamine N-oxide were orally administered to human volunteers, 95% of the dose label was excreted via the kidneys with the majority being trimethylamine N-oxide.
“When radiolabeled TMA or TMAO were orally administered to human volunteers, 95% of the dose label was excreted via the kidneys with the majority being TMAO77.”
From Gut microbiota and cardiovascular disease. (2020) · cites this paper as [77]
Healthy volunteers orally supplemented with choline exhibited higher levels of trimethylamine N-oxide and concomitant enhanced platelet responsiveness and aggregation.
“In a subsequent human feeding study, healthy volunteers (both omnivore and vegan/vegetarian) that were orally supplemented with choline exhibited higher levels of TMAO and concomitant enhanced platelet responsiveness and aggregation77, 118.”
From Gut microbiota and cardiovascular disease. (2020) · cites this paper as [77]
Under normal physiologic conditions, circulating TMAO is rapidly cleared almost exclusively by urinary excretion.
“Under normal physiologic conditions, circulating TMAO is rapidly cleared almost exclusively by urinary excretion [44].”
From Trimethylamine N-oxide: the good, the bad and the unknown. (2016) · cites this paper as [44]
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- Authors
- Al-waiz, M., Mitchell, S. C., Idle, J. R., & Smith, R. L.
- Affiliations
- St Mary's Hospital (GB)
- Venue
- Xenobiotica
- Publisher
- Informa UK Limited
- Published
- 1987-01
- Volume
- 17
- Issue
- 5
- Pages
- 551-558
- ISSN
- 0049-8254 (ISSN-L)
- 1366-5928
- OpenAlex
- W2042398122
- Cited by
- 143
- References
- 28
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 10 · 2023: 6 · 2022: 13 · 2021: 10 · 2020: 11 · 2019: 4 · 2018: 4 · 2017: 7 · 2016: 6 · 2015: 3 · 2014: 2 · 2013: 1 · 2012: 2
- FWCI
- 3.43
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Xenobiotica (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Arabian Gulf University
- Wellcome Trust
- Flinders University
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Polyamine Metabolism and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Keywords
- trimethylamine, trimethylamine N-oxide, urinary excretion, radiolabeled compounds, human metabolism, expired air
- MeSH terms
- Biotransformation, Chromatography, Thin Layer, Humans, Kinetics, Male, Methylamines, Mass Spectrometry
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