Component

SAC-associated protection in mouse cerebral ischemia

Context-specific entity; species, compartment and exposure are stated on each 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. Nrf2 knockout mice did not show the ischemic protection observed with systemic SAC in wild-type mice.

    Experimental context and source evidence
    acting_entity
    mouse-nfe2l2
    availability_state
    machinery_impairment Imported condition classification; unverified.
    dose
    Not specified in accessed abstract
    duration
    Not specified in accessed abstract
    evidence_access
    Primary abstract
    experimental_comparison
    SAC versus ischemic control; wild-type versus Nrf2 knockout
    experimental_model
    Middle cerebral artery occlusion in wild-type and Nrf2 knockout mice
    interpretation_status
    Source-derived research curation; not independent primary verification
    limitations
    Necessity in this model; not proof that every SAC effect requires Nrf2.
    nutrient_topic
    S-allylcysteine collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · S-allyl-L-cysteine / SAC
    organism
    Mus musculus
    plain_language
    Removing the pathway changed the response to SAC.
    primary_references
    [25393425] S-allyl cysteine activates the Nrf2-dependent antioxidant response and protects neurons against ischemic injury in vitro and in vivo. · 2015 · https://pubmed.ncbi.nlm.nih.gov/25393425/ · DOI 10.1111/jnc.12986
    route
    Systemic administration; precise route not retrieved
    tissue_or_cell_type
    Middle cerebral artery occlusion in wild-type and Nrf2 knockout mice
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    S-allylcysteine: sulfur signaling, redox responses and cross-nutrient mechanisms (2026-09-20) · lines 140–147

    AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Middle cerebral artery occlusion in wild-type and Nrf2 knockout mice · source_derived_draft · unverified_draft

    ## s-allylcysteine-mouse-nrf2-required Removing the pathway changed the response to SAC. Nrf2 knockout mice did not show the ischemic protection observed with systemic SAC in wild-type mice. Model: Middle cerebral artery occlusion in wild-type and Nrf2 knockout mice Limitations: Necessity in this model; not proof that every SAC effect requires Nrf2. Evidence access: Primary abstract [25393425] S-allyl cysteine activates the Nrf2-dependent antioxidant response and protects neurons against ischemic injury in vitro and in vivo. · 2015 · https://pubmed.ncbi.nlm.nih.gov/25393425/ · DOI 10.1111/jnc.12986 Structured context: {"organism": "Mus musculus", "tissue_or_cell_type": "Middle cerebral artery occlusion in wild-type and Nrf2 knockout mice", "dose": "Not specified in accessed abstract", "duration": "Not specified in accessed abstract", "route": "Systemic administration; precise route not retrieved", "experimental_comparison": "SAC versus ischemic control; wild-type versus Nrf2 knockout", "acting_entity": "mouse-nfe2l2", "interpretation_status": "Source-derived research curation; not independent primary verification"}
    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