Component

Rat FSL hippocampal/prefrontal p65 K310 acetylation

Rat FSL hippocampal/prefrontal p65 K310 acetylation

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. ALCAR increased acetylated p65 in Flinders Sensitive Line rats, without the same increase in control FRL rats.

    Experimental context and source evidence
    evidence_access
    Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    experimental_contrast
    {"intervention": "ALCAR in FSL and FRL animals", "comparator": "Corresponding saline-treated strain", "endpoint": "ALCAR increased acetylated p65 in Flinders Sensitive Line rats, without the same increase in control FRL rats.", "effect_direction": "mixed", "combination": "single", "conditions": []} Explicit extracted experimental comparison; source-derived draft.
    experimental_model
    100 mg/kg intraperitoneal daily; 21-day biochemical comparison; Fig. 3C, anti-acetyl-K310-p65 assay.
    interpretation_status
    Source-derived curation with stated access limits; ungraded, not independent replication.
    limitations
    Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation.
    nutrient_topic
    Acetyl-L-carnitine collection; exact intervention and molecular form govern interpretation. · Acetyl-L-carnitine
    plain_language
    ALCAR increased acetylated p65 in Flinders Sensitive Line rats, without the same increase in control FRL rats.
    primary_references
    L-acetylcarnitine causes rapid antidepressant effects through the epigenetic induction of mGlu2 receptors. | https://pubmed.ncbi.nlm.nih.gov/23382250/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC3607061/ | https://doi.org/10.1073/pnas.1216100110
    source_locator
    Reviewed reference fsl-p65; H3K27 promoter enrichment and p65 acetylation are distinct measurements. The study did not trace administered ALCAR acetyl atoms into these sites.

    Acetyl-L-carnitine: detailed mechanisms of action (reviewed 6 October 2026) · lines 224–230

    AI-assisted original review of primary studies and clearly identified official records. Exact primary access is stated; no independent replication is claimed. · supports · 100 mg/kg intraperitoneal daily; 21-day biochemical comparison; Fig. 3C, anti-acetyl-K310-p65 assay. · Recorded from source · Recorded from source

    ### fsl-p65 ALCAR increased acetylated p65 in Flinders Sensitive Line rats, without the same increase in control FRL rats. H3K27 promoter enrichment and p65 acetylation are distinct measurements. The study did not trace administered ALCAR acetyl atoms into these sites. Model and exposure: 100 mg/kg intraperitoneal daily; 21-day biochemical comparison; Fig. 3C, anti-acetyl-K310-p65 assay. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: L-acetylcarnitine causes rapid antidepressant effects through the epigenetic induction of mGlu2 receptors. | 2013 | https://pubmed.ncbi.nlm.nih.gov/23382250/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC3607061/ | https://doi.org/10.1073/pnas.1216100110 | Access: Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    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.