Component

Human low-density lipoprotein receptor / LDLR

Human low-density lipoprotein receptor / LDLR. 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. Berberine increased LDLR expression through an ERK-dependent, SREBP-independent post-transcriptional mechanism in human hepatoma cells.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/berberine-research/15531889.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ac2a9817f85e5c1f4f520590f1f2cb1ca820cce75b79120852f616f7ce5bea2f", "start_char": 0, "end_char": 1032, "text_sha256": "ac2a9817f85e5c1f4f520590f1f2cb1ca820cce75b79120852f616f7ce5bea2f"}
    experimental_model
    Human hepatoma mRNA stability/promoter experiments, animal and small clinical arms
    exposure
    Berberine exposure with ERK-dependence assays
    limitations
    Clinical lipid outcomes do not directly prove this molecular route caused the human effect. Cell response was reported independent of SREBP.
    nutrient_topic
    Berberine research collection; topical membership is not evidence of a direct dietary effect. · Berberine
    organism
    Human hepatoma cells for molecular claims
    plain_language
    More LDL receptor can help cells remove LDL from circulation; the mechanism was tested in cells.
    primary_references
    [berberine-p15531889] Berberine is a novel cholesterol-lowering drug working through a unique mechanism distinct from statins. (2004). https://pubmed.ncbi.nlm.nih.gov/15531889/ DOI: 10.1038/nm1135
    tissue_or_cell_type
    LDLR post-transcriptional regulation

    Berberine: metabolism, nutrient connections and drug interactions (2026-09-17) · lines 454–465

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human hepatoma mRNA stability/promoter experiments, animal and small clinical arms · source_derived_draft · unverified_draft

    ### berberine-ldlr-protein Berberine increased LDLR expression through an ERK-dependent, SREBP-independent post-transcriptional mechanism in human hepatoma cells. Condition category: normal nutrient_topic: Berberine research collection; topical membership is not evidence of a direct dietary effect. plain_language: More LDL receptor can help cells remove LDL from circulation; the mechanism was tested in cells. organism: Human hepatoma cells for molecular claims tissue_or_cell_type: LDLR post-transcriptional regulation experimental_model: Human hepatoma mRNA stability/promoter experiments, animal and small clinical arms limitations: Clinical lipid outcomes do not directly prove this molecular route caused the human effect. Cell response was reported independent of SREBP. exposure: Berberine exposure with ERK-dependence assays evidence_span: {"source_cache": "artifacts/berberine-research/15531889.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ac2a9817f85e5c1f4f520590f1f2cb1ca820cce75b79120852f616f7ce5bea2f", "start_char": 0, "end_char": 1032, "text_sha256": "ac2a9817f85e5c1f4f520590f1f2cb1ca820cce75b79120852f616f7ce5bea2f"} [berberine-p15531889] Berberine is a novel cholesterol-lowering drug working through a unique mechanism distinct from statins. (2004). https://pubmed.ncbi.nlm.nih.gov/15531889/ DOI: 10.1038/nm1135
    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