Component

Human oxidative-damage/inflammation biomarkers during ergothioneine intake

Context-specific entity; species, compartment and exposure are stated on each claim.

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. Most oxidative-damage and inflammation marker changes after pure ergothioneine administration were not statistically significant.

    Experimental context and source evidence
    evidence_access
    Primary abstract
    experimental_model
    Healthy-volunteer pharmacokinetic study.
    limitations
    Some downward trends were reported; trends are not confirmed treatment effects.
    nutrient_topic
    Ergothioneine collection; molecular form, preparation, species, exposure and manipulation remain explicit. · L-Ergothioneine
    plain_language
    Measured uptake did not establish a broad biomarker benefit.
    primary_references
    Administration of Pure Ergothioneine to Healthy Human Subjects: Uptake, Metabolism, and Effects on Biomarkers of Oxidative Damage and Inflammation. · 2017 · https://pubmed.ncbi.nlm.nih.gov/27488221/ · DOI 10.1089/ars.2016.6778

    Ergothioneine: transport, redox chemistry and cross-nutrient mechanisms (2026-09-19) · lines 480–486

    AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Healthy-volunteer pharmacokinetic study. · source_derived_draft · unverified_draft

    ## ergothioneine-human-oxidation-null Measured uptake did not establish a broad biomarker benefit. Most oxidative-damage and inflammation marker changes after pure ergothioneine administration were not statistically significant. Model: Healthy-volunteer pharmacokinetic study. Limitations: Some downward trends were reported; trends are not confirmed treatment effects. Evidence access: Primary abstract Administration of Pure Ergothioneine to Healthy Human Subjects: Uptake, Metabolism, and Effects on Biomarkers of Oxidative Damage and Inflammation. · 2017 · https://pubmed.ncbi.nlm.nih.gov/27488221/ · DOI 10.1089/ars.2016.6778
    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.

    Evidence, AI assistance and curation standards