Component

Human plasma TMAO after oral ALCAR

Human plasma TMAO after oral ALCAR

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Oral ALCAR markedly increased plasma TMAO in the 2025 healthy-volunteer study.

    Experimental context and source evidence
    evidence_access
    Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    experimental_contrast
    {"intervention": "Single nominal 1.5-g ALCAR dose", "comparator": "Predose baseline", "endpoint": "Oral ALCAR markedly increased plasma TMAO in the 2025 healthy-volunteer study.", "effect_direction": "increase", "combination": "single", "conditions": []} Explicit extracted experimental comparison; source-derived draft.
    experimental_model
    Single nominal 1.5-g ALCAR; plasma and urine collection over 48 h.
    interpretation_status
    Source-derived curation with stated access limits; ungraded, not independent replication.
    limitations
    Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation.
    nutrient_topic
    Acetyl-L-carnitine collection; exact intervention and molecular form govern interpretation. · Acetyl-L-carnitine
    plain_language
    Oral ALCAR markedly increased plasma TMAO in the 2025 healthy-volunteer study.
    primary_references
    Low Bioavailability and High TMAO Production: Novel Insights Into Acetylcarnitine and Carnitine Metabolism. | https://pubmed.ncbi.nlm.nih.gov/41243468/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC12700042/ | https://doi.org/10.1002/mnfr.70316
    source_locator
    Reviewed reference pk-tmao; Median TMAO increased approximately 2.2 to 47 micromolar; adjusted exposure was comparable to L-carnitine. The acetyl group did not prevent this metabolite signal. Cardiovascular events were not measured.

    Acetyl-L-carnitine: detailed mechanisms of action (reviewed 6 October 2026) · lines 128–134

    AI-assisted original review of primary studies and clearly identified official records. Exact primary access is stated; no independent replication is claimed. · supports · Single nominal 1.5-g ALCAR; plasma and urine collection over 48 h. · Recorded from source · Recorded from source

    ### pk-tmao Oral ALCAR markedly increased plasma TMAO in the 2025 healthy-volunteer study. Median TMAO increased approximately 2.2 to 47 micromolar; adjusted exposure was comparable to L-carnitine. The acetyl group did not prevent this metabolite signal. Cardiovascular events were not measured. Model and exposure: Single nominal 1.5-g ALCAR; plasma and urine collection over 48 h. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Low Bioavailability and High TMAO Production: Novel Insights Into Acetylcarnitine and Carnitine Metabolism. | 2025 | https://pubmed.ncbi.nlm.nih.gov/41243468/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC12700042/ | https://doi.org/10.1002/mnfr.70316 | Access: Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.