Component

Hepatic retinol stores

Independent biological entity. Read linked claims for experimental scope and context.

2 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

Where it participates (unsigned role)

  1. LPS lowered circulating retinol without a detected decrease in liver or kidney retinol in vitamin A-sufficient rats.

    Lipopolysaccharide → Plasma retinol concentration source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    biomarker_context Imported condition classification; unverified.
    experimental_model
    LPS versus saline with food withdrawal.
    limitations
    Acute rat model; not every inflammatory illness follows the same kinetics.
    nutrient_topic
    Vitamin A research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
    organism
    Rattus norvegicus
    plain_language
    A low blood value did not mean the measured tissue stores had been emptied.
    primary_references
    [va-rosales1996] Effects of acute inflammation on plasma retinol, retinol-binding protein, and its mRNA in the liver and kidneys of vitamin A-sufficient rats (1996). https://pubmed.ncbi.nlm.nih.gov/8725149/ DOI: 10.1016/s0022-2275(20)42007-3
    tissue_or_cell_type
    Plasma, liver and kidney
    trigger_kind
    biomarker_context Imported condition classification; unverified.

    Vitamin A: forms, mechanisms, deficiency and excess (2026-09-17) · lines 1674–1683

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · LPS versus saline with food withdrawal. · source_derived_draft · unverified_draft

    ### va-lps-lowers-retinol-with-stores LPS lowered circulating retinol without a detected decrease in liver or kidney retinol in vitamin A-sufficient rats. Condition category: biomarker_context nutrient_topic: Vitamin A research collection; topical membership is not evidence of a direct dietary effect. plain_language: A low blood value did not mean the measured tissue stores had been emptied. organism: Rattus norvegicus tissue_or_cell_type: Plasma, liver and kidney experimental_model: LPS versus saline with food withdrawal. limitations: Acute rat model; not every inflammatory illness follows the same kinetics. [va-rosales1996] Effects of acute inflammation on plasma retinol, retinol-binding protein, and its mRNA in the liver and kidneys of vitamin A-sufficient rats (1996). https://pubmed.ncbi.nlm.nih.gov/8725149/ DOI: 10.1016/s0022-2275(20)42007-3
    Complete structured claim and evidence
  2. Serum-retinol and isotope-modelled liver-store classifications disagreed in Thai and Zambian children; inflammation adjustment reduced false positives in the latter.

    Experimental context and source evidence
    availability_state
    biomarker_context Imported condition classification; unverified.
    experimental_model
    37 Thai and 128 Zambian children.
    limitations
    Isotope-derived liver reserves are model estimates; these data do not establish universal diagnostic performance.
    nutrient_topic
    Vitamin A research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
    organism
    Homo sapiens
    plain_language
    Neither a normal nor a low serum result fully described reserves in these cohorts.
    primary_references
    [va-suri2015] Serum retinol concentrations demonstrate high specificity after correcting for inflammation but questionable sensitivity compared with liver stores calculated from isotope dilution in determining vitamin A deficiency in Thai and Zambian children (2015). https://pubmed.ncbi.nlm.nih.gov/26447158/ DOI: 10.3945/ajcn.115.113050
    tissue_or_cell_type
    Serum and inferred liver stores
    trigger_kind
    biomarker_context Imported condition classification; unverified.

    Vitamin A: forms, mechanisms, deficiency and excess (2026-09-17) · lines 1696–1705

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 37 Thai and 128 Zambian children. · source_derived_draft · unverified_draft

    ### va-serum-versus-isotope-classification Serum-retinol and isotope-modelled liver-store classifications disagreed in Thai and Zambian children; inflammation adjustment reduced false positives in the latter. Condition category: biomarker_context nutrient_topic: Vitamin A research collection; topical membership is not evidence of a direct dietary effect. plain_language: Neither a normal nor a low serum result fully described reserves in these cohorts. organism: Homo sapiens tissue_or_cell_type: Serum and inferred liver stores experimental_model: 37 Thai and 128 Zambian children. limitations: Isotope-derived liver reserves are model estimates; these data do not establish universal diagnostic performance. [va-suri2015] Serum retinol concentrations demonstrate high specificity after correcting for inflammation but questionable sensitivity compared with liver stores calculated from isotope dilution in determining vitamin A deficiency in Thai and Zambian children (2015). https://pubmed.ncbi.nlm.nih.gov/26447158/ DOI: 10.3945/ajcn.115.113050
    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