Component

Salmonella-induced ERK/JNK activation in Caco-2 cells

Species, preparation, dose and limitations are retained on linked claims.

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. Bromelain dose-dependently blocked Salmonella Typhimurium-induced ERK1/2 and JNK activation in human Caco-2 cells.

    Experimental context and source evidence
    dose
    Bromelain with Salmonella Typhimurium
    duration
    Acute infection assay
    evidence_access
    Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    evidence_scope
    literature_reviewed; model-specific source-derived curation
    experimental_model
    Human Caco-2 intestinal epithelial cells
    limitations
    Blocking these kinase signals did not prevent invasion or barrier-resistance loss in the same study.
    nutrient_topic
    Bromelain chapter; interacting nutrients, drugs, peptides and proteins retain their experimental settings. · Bromelain
    organism
    Human Caco-2 intestinal epithelial cells
    plain_language
    Bromelain dose-dependently blocked Salmonella Typhimurium-induced ERK1/2 and JNK activation in human Caco-2 cells.
    primary_references
    Proteolytic inhibition of Salmonella enterica serovar typhimurium-induced activation of the mitogen-activated protein kinases ERK and JNK in cultured human intestinal cells. (2002). https://pubmed.ncbi.nlm.nih.gov/11748167/ DOI: 10.1128/IAI.70.1.86-95.2002
    route
    In vitro
    tissue
    ERK1/2 and JNK phosphorylation

    Bromelain: mechanism of action and interactions (2026-09-20) · lines 77–86

    Original AI-assisted source-specific curation with primary-study citations, model, exposure, route, duration, negative findings and limitations preserved. Not publisher full text. · supports · Human Caco-2 intestinal epithelial cells · source_derived_draft · unverified_draft

    ## bromelain-mapk-blockade Bromelain dose-dependently blocked Salmonella Typhimurium-induced ERK1/2 and JNK activation in human Caco-2 cells. Model/species: Human Caco-2 intestinal epithelial cells Tissue/system: ERK1/2 and JNK phosphorylation Exposure: Bromelain with Salmonella Typhimurium Route: In vitro Duration: Acute infection assay Limits: Blocking these kinase signals did not prevent invasion or barrier-resistance loss in the same study. Primary reference: Proteolytic inhibition of Salmonella enterica serovar typhimurium-induced activation of the mitogen-activated protein kinases ERK and JNK in cultured human intestinal cells. (2002). https://pubmed.ncbi.nlm.nih.gov/11748167/ DOI: 10.1128/IAI.70.1.86-95.2002 Access: Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    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