Component

Plasma glutathione in Ggt1-null mice

Plasma glutathione in Ggt1-null mice. Species, exposure and limitations are retained in each linked 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. Plasma GSH was about sixfold higher in Ggt1-null mice.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/glutathione-research/8755578.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "94d2520bc0124611c649d943ab9acd9cdf73cd3cb99d66640338a57bda6f6dfb", "start_char": 0, "end_char": 1159, "text_sha256": "94d2520bc0124611c649d943ab9acd9cdf73cd3cb99d66640338a57bda6f6dfb"}
    experimental_model
    Targeted GGT gene disruption and NAC rescue
    exposure
    Ggt1-null versus wild type; oral NAC
    limitations
    Severe genetic salvage defect; high extracellular GSH did not mean adequate tissue stores.
    nutrient_topic
    Glutathione research collection; topical membership is not evidence of a direct dietary effect. · GSH
    organism
    Mouse
    plain_language
    High plasma glutathione did not rule out a metabolic defect.
    primary_references
    [glutathione-p8755578] Growth retardation and cysteine deficiency in gamma-glutamyl transpeptidase-deficient mice. (1996). https://pubmed.ncbi.nlm.nih.gov/8755578/ DOI: 10.1073/pnas.93.15.7923
    tissue_or_cell_type
    Plasma, urine, eye, liver and pancreas
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Glutathione: metabolism, signaling and nutrient connections (2026-09-17) · lines 671–682

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Targeted GGT gene disruption and NAC rescue · source_derived_draft · unverified_draft

    ### glutathione-ggt-plasma-high Plasma GSH was about sixfold higher in Ggt1-null mice. Condition category: machinery_impairment nutrient_topic: Glutathione research collection; topical membership is not evidence of a direct dietary effect. plain_language: High plasma glutathione did not rule out a metabolic defect. organism: Mouse tissue_or_cell_type: Plasma, urine, eye, liver and pancreas experimental_model: Targeted GGT gene disruption and NAC rescue limitations: Severe genetic salvage defect; high extracellular GSH did not mean adequate tissue stores. exposure: Ggt1-null versus wild type; oral NAC evidence_span: {"source_cache": "artifacts/glutathione-research/8755578.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "94d2520bc0124611c649d943ab9acd9cdf73cd3cb99d66640338a57bda6f6dfb", "start_char": 0, "end_char": 1159, "text_sha256": "94d2520bc0124611c649d943ab9acd9cdf73cd3cb99d66640338a57bda6f6dfb"} [glutathione-p8755578] Growth retardation and cysteine deficiency in gamma-glutamyl transpeptidase-deficient mice. (1996). https://pubmed.ncbi.nlm.nih.gov/8755578/ DOI: 10.1073/pnas.93.15.7923
    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