Component

Human urinary apigenin conjugate recovery

Human urinary apigenin conjugate recovery

3 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. Chamomile tea produced the same two plasma conjugates with observed peaks at 2 hours and approximately 34% urinary recovery of measured metabolites over 24 hours.

    Experimental context and source evidence
    evidence_access
    Full original primary-paper PDF, Methods, Results and Tables 1–7 reviewed; authentic-standard HPLC-MS analysis. PDF obtained from a public mirror; DOI and article identity verified.
    experimental_model
    Four men; tea containing 13.4 micromoles apigenin 7-O-glucoside and 1.2 micromoles parent.
    interpretation_status
    Recorded from source 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
    Apigenin collection; exact intervention and molecular form govern interpretation. · Apigenin
    plain_language
    Chamomile tea produced the same two plasma conjugates with observed peaks at 2 hours and approximately 34% urinary recovery of measured metabolites over 24 hours.
    primary_references
    Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. | https://pubmed.ncbi.nlm.nih.gov/35452808/ | https://doi.org/10.1016/j.freeradbiomed.2022.04.007
    source_locator
    Reviewed reference api-chamomile-pk; Section 3.3.4. The different glycoside and food matrix preclude equating this with a parent capsule.

    Apigenin: detailed mechanisms of action (reviewed 10 October 2026) · lines 77–83

    AI-assisted original curation of primary studies; claim-local access and experimental limitations stated. Includes original-draft correction history. No independent replication claimed. · supports · Four men; tea containing 13.4 micromoles apigenin 7-O-glucoside and 1.2 micromoles parent. · Recorded from source · Recorded from source

    ### api-chamomile-pk Chamomile tea produced the same two plasma conjugates with observed peaks at 2 hours and approximately 34% urinary recovery of measured metabolites over 24 hours. Section 3.3.4. The different glycoside and food matrix preclude equating this with a parent capsule. Model and exposure: Four men; tea containing 13.4 micromoles apigenin 7-O-glucoside and 1.2 micromoles parent. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. | 2022 | https://pubmed.ncbi.nlm.nih.gov/35452808/ | https://doi.org/10.1016/j.freeradbiomed.2022.04.007 | Access: Full original primary-paper PDF, Methods, Results and Tables 1–7 reviewed; authentic-standard HPLC-MS analysis. PDF obtained from a public mirror; DOI and article identity verified.
    Complete structured claim and evidence
  2. The same aglycone exposure yielded 0.9 ± 0.6 micromoles of measured urinary glucuronides over 24 hours, about 0.5% of intake.

    Apigenin → Human urinary apigenin conjugate recovery Recorded from sourceungraded
    Experimental context and source evidence
    evidence_access
    Full original primary-paper PDF, Methods, Results and Tables 1–7 reviewed; authentic-standard HPLC-MS analysis. PDF obtained from a public mirror; DOI and article identity verified.
    experimental_model
    Three healthy men; authentic-standard HPLC-MS.
    interpretation_status
    Recorded from source 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
    Apigenin collection; exact intervention and molecular form govern interpretation. · Apigenin
    plain_language
    The same aglycone exposure yielded 0.9 ± 0.6 micromoles of measured urinary glucuronides over 24 hours, about 0.5% of intake.
    primary_references
    Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. | https://pubmed.ncbi.nlm.nih.gov/35452808/ | https://doi.org/10.1016/j.freeradbiomed.2022.04.007
    source_locator
    Reviewed reference api-parent-urine; Recovery of selected metabolites is not an absolute bioavailability measurement.

    Apigenin: detailed mechanisms of action (reviewed 10 October 2026) · lines 37–43

    AI-assisted original curation of primary studies; claim-local access and experimental limitations stated. Includes original-draft correction history. No independent replication claimed. · supports · Three healthy men; authentic-standard HPLC-MS. · Recorded from source · Recorded from source

    ### api-parent-urine The same aglycone exposure yielded 0.9 ± 0.6 micromoles of measured urinary glucuronides over 24 hours, about 0.5% of intake. Recovery of selected metabolites is not an absolute bioavailability measurement. Model and exposure: Three healthy men; authentic-standard HPLC-MS. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. | 2022 | https://pubmed.ncbi.nlm.nih.gov/35452808/ | https://doi.org/10.1016/j.freeradbiomed.2022.04.007 | Access: Full original primary-paper PDF, Methods, Results and Tables 1–7 reviewed; authentic-standard HPLC-MS analysis. PDF obtained from a public mirror; DOI and article identity verified.
    Complete structured claim and evidence
  3. Measured urinary apigenin metabolites after the initial parsley drink averaged 11.2% of ingested flavone equivalents.

    Experimental context and source evidence
    evidence_access
    Full original primary-paper PDF, Methods, Results and Tables 1–7 reviewed; authentic-standard HPLC-MS analysis. PDF obtained from a public mirror; DOI and article identity verified.
    experimental_model
    Four men; 0–24-hour urine.
    interpretation_status
    Recorded from source 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
    Apigenin collection; exact intervention and molecular form govern interpretation. · Apigenin
    plain_language
    Measured urinary apigenin metabolites after the initial parsley drink averaged 11.2% of ingested flavone equivalents.
    primary_references
    Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. | https://pubmed.ncbi.nlm.nih.gov/35452808/ | https://doi.org/10.1016/j.freeradbiomed.2022.04.007
    source_locator
    Reviewed reference api-parsley-urine; The larger repeated-intake series gave 17.2 ± 9.8% recovery across 17 intakes, with greater inter-person than within-person variation. Neither figure is an intravenous-reference absolute bioavailability estimate.

    Apigenin: detailed mechanisms of action (reviewed 10 October 2026) · lines 61–67

    AI-assisted original curation of primary studies; claim-local access and experimental limitations stated. Includes original-draft correction history. No independent replication claimed. · supports · Four men; 0–24-hour urine. · Recorded from source · Recorded from source

    ### api-parsley-urine Measured urinary apigenin metabolites after the initial parsley drink averaged 11.2% of ingested flavone equivalents. The larger repeated-intake series gave 17.2 ± 9.8% recovery across 17 intakes, with greater inter-person than within-person variation. Neither figure is an intravenous-reference absolute bioavailability estimate. Model and exposure: Four men; 0–24-hour urine. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. | 2022 | https://pubmed.ncbi.nlm.nih.gov/35452808/ | https://doi.org/10.1016/j.freeradbiomed.2022.04.007 | Access: Full original primary-paper PDF, Methods, Results and Tables 1–7 reviewed; authentic-standard HPLC-MS analysis. PDF obtained from a public mirror; DOI and article identity verified.
    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.