Component

Mouse 5-HT3 receptor-channel complex

Native N1E-115-cell 5-HT3 channel; subunit composition unresolved in the accessed source.

3 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. 10-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells.

    10-Gingerol → Mouse 5-HT3 receptor-channel complex source_derived_draftungraded
    Experimental context and source evidence
    dose
    Concentration-dependent gingerol application; exact range not in accessed abstract
    duration
    Not specified in accessed abstract
    evidence_access
    Primary PubMed abstract.
    evidence_scope
    literature_reviewed; model-specific source-derived curation, not universally established human effects
    experimental_model
    Mouse N1E-115 neuroblastoma cells
    limitations
    Cation flux is a functional assay, not a demonstrated orthosteric binding site or clinical antiemetic response.
    nutrient_topic
    Gingerols collection; each molecular form and experimental preparation remains explicit. · Gingerols
    organism
    Mouse N1E-115 neuroblastoma cells
    plain_language
    10-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells.
    primary_references
    Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. (2006). https://pubmed.ncbi.nlm.nih.gov/16364290/ DOI: 10.1016/j.ejphar.2005.10.049
    route
    In vitro addition
    tissue
    Native 5-HT3 receptor-channel complex

    Gingerols: mechanisms, molecular forms and cross-actor connections (2026-09-20) · lines 118–127

    Original AI-assisted curation of thirteen primary research papers; study-specific PubMed/DOI links and limitations retained. Not publisher full text. · supports · Mouse N1E-115 neuroblastoma cells · source_derived_draft · unverified_draft

    ## gingerols-10-5ht3-flux 10-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells. Model/species: Mouse N1E-115 neuroblastoma cells Tissue: Native 5-HT3 receptor-channel complex Exposure: Concentration-dependent gingerol application; exact range not in accessed abstract Route: In vitro addition Duration: Not specified in accessed abstract Limits: Cation flux is a functional assay, not a demonstrated orthosteric binding site or clinical antiemetic response. Primary reference: Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. (2006). https://pubmed.ncbi.nlm.nih.gov/16364290/ DOI: 10.1016/j.ejphar.2005.10.049 Access: Primary PubMed abstract.
    Complete structured claim and evidence
  2. 6-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells.

    6-Gingerol → Mouse 5-HT3 receptor-channel complex source_derived_draftungraded
    Experimental context and source evidence
    dose
    Concentration-dependent gingerol application; exact range not in accessed abstract
    duration
    Not specified in accessed abstract
    evidence_access
    Primary PubMed abstract.
    evidence_scope
    literature_reviewed; model-specific source-derived curation, not universally established human effects
    experimental_model
    Mouse N1E-115 neuroblastoma cells
    limitations
    Cation flux is a functional assay, not a demonstrated orthosteric binding site or clinical antiemetic response.
    nutrient_topic
    Gingerols collection; each molecular form and experimental preparation remains explicit. · Gingerols
    organism
    Mouse N1E-115 neuroblastoma cells
    plain_language
    6-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells.
    primary_references
    Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. (2006). https://pubmed.ncbi.nlm.nih.gov/16364290/ DOI: 10.1016/j.ejphar.2005.10.049
    route
    In vitro addition
    tissue
    Native 5-HT3 receptor-channel complex

    Gingerols: mechanisms, molecular forms and cross-actor connections (2026-09-20) · lines 52–61

    Original AI-assisted curation of thirteen primary research papers; study-specific PubMed/DOI links and limitations retained. Not publisher full text. · supports · Mouse N1E-115 neuroblastoma cells · source_derived_draft · unverified_draft

    ## gingerols-6-5ht3-flux 6-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells. Model/species: Mouse N1E-115 neuroblastoma cells Tissue: Native 5-HT3 receptor-channel complex Exposure: Concentration-dependent gingerol application; exact range not in accessed abstract Route: In vitro addition Duration: Not specified in accessed abstract Limits: Cation flux is a functional assay, not a demonstrated orthosteric binding site or clinical antiemetic response. Primary reference: Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. (2006). https://pubmed.ncbi.nlm.nih.gov/16364290/ DOI: 10.1016/j.ejphar.2005.10.049 Access: Primary PubMed abstract.
    Complete structured claim and evidence
  3. 8-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells.

    8-Gingerol → Mouse 5-HT3 receptor-channel complex source_derived_draftungraded
    Experimental context and source evidence
    dose
    Concentration-dependent gingerol application; exact range not in accessed abstract
    duration
    Not specified in accessed abstract
    evidence_access
    Primary PubMed abstract.
    evidence_scope
    literature_reviewed; model-specific source-derived curation, not universally established human effects
    experimental_model
    Mouse N1E-115 neuroblastoma cells
    limitations
    Cation flux is a functional assay, not a demonstrated orthosteric binding site or clinical antiemetic response.
    nutrient_topic
    Gingerols collection; each molecular form and experimental preparation remains explicit. · Gingerols
    organism
    Mouse N1E-115 neuroblastoma cells
    plain_language
    8-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells.
    primary_references
    Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. (2006). https://pubmed.ncbi.nlm.nih.gov/16364290/ DOI: 10.1016/j.ejphar.2005.10.049
    route
    In vitro addition
    tissue
    Native 5-HT3 receptor-channel complex

    Gingerols: mechanisms, molecular forms and cross-actor connections (2026-09-20) · lines 85–94

    Original AI-assisted curation of thirteen primary research papers; study-specific PubMed/DOI links and limitations retained. Not publisher full text. · supports · Mouse N1E-115 neuroblastoma cells · source_derived_draft · unverified_draft

    ## gingerols-8-5ht3-flux 8-Gingerol inhibited 5-HT3-mediated cation influx in N1E-115 cells. Model/species: Mouse N1E-115 neuroblastoma cells Tissue: Native 5-HT3 receptor-channel complex Exposure: Concentration-dependent gingerol application; exact range not in accessed abstract Route: In vitro addition Duration: Not specified in accessed abstract Limits: Cation flux is a functional assay, not a demonstrated orthosteric binding site or clinical antiemetic response. Primary reference: Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. (2006). https://pubmed.ncbi.nlm.nih.gov/16364290/ DOI: 10.1016/j.ejphar.2005.10.049 Access: Primary PubMed abstract.
    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