Component

Rat glucose transporter 9 / Slc2a9

Rat glucose transporter 9 / Slc2a9. 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 reduced renal Rat glucose transporter 9 / Slc2a9 mRNA and protein in hyperuricemic rats.

    Mangiferin → Rat glucose transporter 9 / Slc2a9 source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/mangiferin-research/26228630.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d7d497620fe96b2161af66b3d58b0a4ef8208f10f6d669fc680b85aa38b8d85c", "start_char": 0, "end_char": 1633, "text_sha256": "d7d497620fe96b2161af66b3d58b0a4ef8208f10f6d669fc680b85aa38b8d85c"}
    experimental_model
    Experimental hyperuricemia in rodents
    exposure
    Mangiferin 1.5-24 mg/kg; potassium-oxonate rat model
    limitations
    Abundance changes do not prove direct transporter blockade or clinical gout efficacy.
    nutrient_topic
    Mangiferin research collection; topical membership is not evidence of a direct dietary effect. · Mangiferin
    organism
    Rattus norvegicus for transporter findings
    plain_language
    Less of a urate-reabsorption transporter was measured.
    primary_references
    [mangiferin-p26228630] Mangiferin Inhibits Renal Urate Reabsorption by Modulating Urate Transporters in Experimental Hyperuricemia. (2015). https://pubmed.ncbi.nlm.nih.gov/26228630/ DOI: 10.1248/bpb.b15-00402
    tissue_or_cell_type
    Kidney

    Mangiferin: metabolism, signaling and nutrient connections (2026-09-17) · lines 939–950

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Experimental hyperuricemia in rodents · source_derived_draft · unverified_draft

    ### mangiferin-rat-slc2a9 Mangiferin reduced renal Rat glucose transporter 9 / Slc2a9 mRNA and protein in hyperuricemic rats. Condition category: normal nutrient_topic: Mangiferin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Less of a urate-reabsorption transporter was measured. organism: Rattus norvegicus for transporter findings tissue_or_cell_type: Kidney experimental_model: Experimental hyperuricemia in rodents limitations: Abundance changes do not prove direct transporter blockade or clinical gout efficacy. exposure: Mangiferin 1.5-24 mg/kg; potassium-oxonate rat model evidence_span: {"source_cache": "artifacts/mangiferin-research/26228630.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d7d497620fe96b2161af66b3d58b0a4ef8208f10f6d669fc680b85aa38b8d85c", "start_char": 0, "end_char": 1633, "text_sha256": "d7d497620fe96b2161af66b3d58b0a4ef8208f10f6d669fc680b85aa38b8d85c"} [mangiferin-p26228630] Mangiferin Inhibits Renal Urate Reabsorption by Modulating Urate Transporters in Experimental Hyperuricemia. (2015). https://pubmed.ncbi.nlm.nih.gov/26228630/ DOI: 10.1248/bpb.b15-00402
    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