Component

Calculated tyrosine brain influx in PKU

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.

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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. In ten PKU patients, 300 mg/kg/day tyrosine transiently raised calculated brain tyrosine influx from 27% to 90% of normal, but it remained below 70% for half the sampled period.

    L-Tyrosine → Calculated tyrosine brain influx in PKU source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    biomarker_context Imported condition classification; unverified.
    evidence_access
    Primary abstract
    experimental_model
    Forty-eight-hour human study with tyrosine on day two and calculated transport estimates.
    limitations
    Brain influx was modeled, not directly measured; high phenylalanine and other competing amino acids remain part of the model.
    nutrient_topic
    L-Phenylalanine collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · L-Phenylalanine
    plain_language
    A blood rise after supplementation need not provide steady predicted brain delivery.
    primary_references
    Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acids. · 2001 · https://pubmed.ncbi.nlm.nih.gov/11562623/ · DOI 10.1067/mpd.2001.117576
    trigger_kind
    biomarker_context Imported condition classification; unverified.

    L-Phenylalanine: transport, protein synthesis, cofactor recycling and cross-nutrient mechanisms (2026-09-19) · lines 198–204

    AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Forty-eight-hour human study with tyrosine on day two and calculated transport estimates. · source_derived_draft · unverified_draft

    ## l-phenylalanine-tyrosine-brain-estimate A blood rise after supplementation need not provide steady predicted brain delivery. In ten PKU patients, 300 mg/kg/day tyrosine transiently raised calculated brain tyrosine influx from 27% to 90% of normal, but it remained below 70% for half the sampled period. Model: Forty-eight-hour human study with tyrosine on day two and calculated transport estimates. Limitations: Brain influx was modeled, not directly measured; high phenylalanine and other competing amino acids remain part of the model. Evidence access: Primary abstract Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acids. · 2001 · https://pubmed.ncbi.nlm.nih.gov/11562623/ · DOI 10.1067/mpd.2001.117576
    Complete structured claim and evidence

In the sources

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    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