Component

Allicin injury in human A549 and Beas-2B cultures

Allicin injury in human A549 and Beas-2B cultures. Interpret through the linked study species, preparation, exposure and measured endpoint.

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. Added extracellular glutathione reduced injury from allicin in Human A549/Beas-2B epithelial cultures.

    Experimental context and source evidence
    evidence_access
    Primary full text available; selected claim-relevant methods, results, tables/figures and limitations reviewed. Supplemental proteome and all secondary findings are not exhaustively extracted.
    experimental_condition
    Same allicin exposure without added GSH present · Allicin Condition belongs to the full experimental contrast; do not separate a joint intervention.
    experimental_condition
    Same allicin exposure without added GSH added extracellularly · GSH Condition belongs to the full experimental contrast; do not separate a joint intervention.
    experimental_contrast
    {"intervention": "Allicin plus 1 mM extracellular GSH", "comparator": "Same allicin exposure without added GSH", "endpoint": "Added extracellular glutathione reduced injury from allicin in Human A549/Beas-2B epithelial cultures.", "effect_direction": "decrease", "combination": "joint", "conditions": [{"entity_slug": "glutathione", "state": "added extracellularly"}, {"entity_slug": "allicin", "state": "present"}]} Explicit extracted experimental comparison; source-derived draft.
    experimental_model
    Human A549/Beas-2B epithelial cultures; 1 mM extracellular GSH, direct allicin exposure; metabolic/LDH assays.
    interpretation_status
    Source-derived extraction of a fact-checked reference; access is explicit, not independent raw-data verification.
    limitations
    Quenching changes free exposure; it is not proof of intracellular repair or a validated physiological plasma GSH level.
    plain_language
    Added extracellular glutathione reduced injury from allicin in Human A549/Beas-2B epithelial cultures.
    primary_references
    Diallylthiosulfinate (Allicin), a Volatile Antimicrobial from Garlic (Allium sativum), Kills Human Lung Pathogenic Bacteria, Including MDR Strains, as a Vapor. | 2017 | DOI 10.3390/molecules22101711 | PMID 29023413 | https://pubmed.ncbi.nlm.nih.gov/29023413/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC6151386/ | https://doi.org/10.3390/molecules22101711
    source_locator
    Reviewed reference lines 65-65; exact primary location described in quoted passage where extracted.

    Allicin: detailed mechanisms of action (reviewed 5 October 2026) · lines 65–65

    Original AI-assisted review of primary studies and, where relevant, official regulatory records. Access level is retained per claim. Corrections, null results and unresolved questions remain explicit. Not publisher full text or independent replication. · supports · Human A549/Beas-2B epithelial cultures; 1 mM extracellular GSH, direct allicin exposure; metabolic/LDH assays. · source_derived_draft · unverified_draft

    **Laboratory antimicrobial activity.** Purified allicin inhibited multiple tested respiratory bacterial isolates, including some resistant to clinical antibiotics; susceptibility varied by organism and assay. The same investigation measured mammalian-cell and rat-lung-slice toxicity. Added glutathione reduced toxicity in those models. The experimental 1-mM glutathione condition must not be presented as a validated normal plasma concentration or a safe inhalation regimen. Luminal or surface accessibility is a hypothesis about delivery, not a calculation proving efficacy from nominal dose divided by fluid volume. [Reiter 2017](https://pmc.ncbi.nlm.nih.gov/articles/PMC6151386/)
    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.