Component

Mouse carnitine transporter Octn2 / Slc22a5

Mouse carnitine transporter Octn2 / Slc22a5. Species, exposure and limitations are retained in each linked 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. Mangiferin increased renal Mouse carnitine transporter Octn2 / Slc22a5 expression in the hyperuricemic mice.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/mangiferin-research/21348301.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7c27a677db4a27cc088cfd83ce3506ffdfd866ef91250732b1dd2287d4cf4b58", "start_char": 0, "end_char": 1981, "text_sha256": "7c27a677db4a27cc088cfd83ce3506ffdfd866ef91250732b1dd2287d4cf4b58"}
    experimental_model
    Seven-day potassium-oxonate hyperuricemia model
    exposure
    Mangiferin 50, 100 or 200 mg/kg orally
    limitations
    Animal expression findings; no human carnitine-retention or gout-treatment conclusion.
    nutrient_topic
    Mangiferin research collection; topical membership is not evidence of a direct dietary effect. · Mangiferin
    organism
    Mus musculus
    plain_language
    A transporter linked to carnitine also responded.
    primary_references
    [mangiferin-p21348301] [Mangiferin promotes uric acid excretion and kidney function improvement and modulates related renal transporters in hyperuricemic mice]. (2010). https://pubmed.ncbi.nlm.nih.gov/21348301/
    tissue_or_cell_type
    Kidney

    Mangiferin: metabolism, signaling and nutrient connections (2026-09-17) · lines 1004–1015

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Seven-day potassium-oxonate hyperuricemia model · source_derived_draft · unverified_draft

    ### mangiferin-mouse-slc22a5 Mangiferin increased renal Mouse carnitine transporter Octn2 / Slc22a5 expression in the hyperuricemic mice. Condition category: normal nutrient_topic: Mangiferin research collection; topical membership is not evidence of a direct dietary effect. plain_language: A transporter linked to carnitine also responded. organism: Mus musculus tissue_or_cell_type: Kidney experimental_model: Seven-day potassium-oxonate hyperuricemia model limitations: Animal expression findings; no human carnitine-retention or gout-treatment conclusion. exposure: Mangiferin 50, 100 or 200 mg/kg orally evidence_span: {"source_cache": "artifacts/mangiferin-research/21348301.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7c27a677db4a27cc088cfd83ce3506ffdfd866ef91250732b1dd2287d4cf4b58", "start_char": 0, "end_char": 1981, "text_sha256": "7c27a677db4a27cc088cfd83ce3506ffdfd866ef91250732b1dd2287d4cf4b58"} [mangiferin-p21348301] [Mangiferin promotes uric acid excretion and kidney function improvement and modulates related renal transporters in hyperuricemic mice]. (2010). https://pubmed.ncbi.nlm.nih.gov/21348301/
    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