Component

Mouse muscle fatty-acid oxidation

Mouse muscle fatty-acid oxidation. 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. Soleus fatty-acid oxidation was about 30% higher in Acacb-null mice than in wild-type mice.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/biotin-research/11283375.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d8998a50f9e50b7528afe992760b547dcf705d04f873f0f4f11ed81e71b48249", "start_char": 0, "end_char": 894, "text_sha256": "d8998a50f9e50b7528afe992760b547dcf705d04f873f0f4f11ed81e71b48249"}
    experimental_model
    Acacb-knockout mice compared with wild type
    exposure
    Genetic deletion
    limitations
    Loss of one enzyme in mice is not dietary biotin deficiency, which can affect several enzymes; this is not evidence for inducing deficiency to change body weight.
    nutrient_topic
    Biotin research collection; topical membership is not evidence of a direct dietary effect. · Biotin
    organism
    Mus musculus
    plain_language
    The enzyme deletion changed fuel use in mouse muscle.
    primary_references
    [b7-p11283375] Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2. (2001). https://pubmed.ncbi.nlm.nih.gov/11283375/ DOI: 10.1126/science.1056843
    tissue_or_cell_type
    Heart, skeletal muscle and adipose tissue
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Biotin: carboxylases, recycling, deficiency and nutrient interactions (2026-09-17) · lines 728–739

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Acacb-knockout mice compared with wild type · source_derived_draft · unverified_draft

    ### b7-acc2-null-oxidation Soleus fatty-acid oxidation was about 30% higher in Acacb-null mice than in wild-type mice. Condition category: machinery_impairment nutrient_topic: Biotin research collection; topical membership is not evidence of a direct dietary effect. plain_language: The enzyme deletion changed fuel use in mouse muscle. organism: Mus musculus tissue_or_cell_type: Heart, skeletal muscle and adipose tissue experimental_model: Acacb-knockout mice compared with wild type limitations: Loss of one enzyme in mice is not dietary biotin deficiency, which can affect several enzymes; this is not evidence for inducing deficiency to change body weight. exposure: Genetic deletion evidence_span: {"source_cache": "artifacts/biotin-research/11283375.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d8998a50f9e50b7528afe992760b547dcf705d04f873f0f4f11ed81e71b48249", "start_char": 0, "end_char": 894, "text_sha256": "d8998a50f9e50b7528afe992760b547dcf705d04f873f0f4f11ed81e71b48249"} [b7-p11283375] Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2. (2001). https://pubmed.ncbi.nlm.nih.gov/11283375/ DOI: 10.1126/science.1056843
    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