Component

Whole-body lipolytic flux

Context-specific entity; species, compartment and exposure are stated on each claim.

2 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. Lipolysis increased approximately 2.5-fold over 60 hours.

    Experimental context and source evidence
    evidence_access
    Primary abstract
    experimental_model
    Six men; isotope tracers and indirect calorimetry during a 60-hour fast.
    limitations
    Protocol-specific fluxes; no universal hour-by-hour threshold.
    nutrient_topic
    Fasting physiological-state collection; human protocols, cellular deprivation and refeeding are distinguished. · Fasting / abstention from energy intake
    plain_language
    Stored fat supplied more circulating fuel.
    primary_references
    Fuel and energy metabolism in fasting humans. · 1994 · https://pubmed.ncbi.nlm.nih.gov/8017334/ · DOI 10.1093/ajcn/60.1.29

    Fasting: fuel switching, nutrient sensing, ketone signaling, nutrient dependencies and refeeding (2026-09-18) · lines 24–30

    AI-assisted research curation; primary-abstract references and experimental limitations individually identified. Not publisher full text. · supports · Six men; isotope tracers and indirect calorimetry during a 60-hour fast. · source_derived_draft · unverified_draft

    ## fast-lipolysis Stored fat supplied more circulating fuel. Lipolysis increased approximately 2.5-fold over 60 hours. Model: Six men; isotope tracers and indirect calorimetry during a 60-hour fast. Limitations: Protocol-specific fluxes; no universal hour-by-hour threshold. Evidence access: Primary abstract Fuel and energy metabolism in fasting humans. · 1994 · https://pubmed.ncbi.nlm.nih.gov/8017334/ · DOI 10.1093/ajcn/60.1.29
    Complete structured claim and evidence

Where it participates (unsigned role)

  1. Adipose PDE3B transcript levels decreased after fasting, with and without GH blockade.

    Experimental context and source evidence
    evidence_access
    Primary full-text Results: Regulation of lipolysis, DOI 10.1210/jc.2016-3835
    experimental_model
    Nine obese men; adipose biopsy after 72-hour fast.
    limitations
    Transcript level is not direct PDE3B enzyme activity.
    nutrient_topic
    Fasting physiological-state collection; human protocols, cellular deprivation and refeeding are distinguished. · Fasting / abstention from energy intake
    plain_language
    A molecular brake on fat release changed.
    primary_references
    Substrate Metabolism and Insulin Sensitivity During Fasting in Obese Human Subjects: Impact of GH Blockade. · 2017 · https://pubmed.ncbi.nlm.nih.gov/28324055/ · DOI 10.1210/jc.2016-3835

    Fasting: fuel switching, nutrient sensing, ketone signaling, nutrient dependencies and refeeding (2026-09-18) · lines 224–230

    AI-assisted research curation; primary-abstract references and experimental limitations individually identified. Not publisher full text. · supports · Nine obese men; adipose biopsy after 72-hour fast. · source_derived_draft · unverified_draft

    ## fast-adipose-pde3b A molecular brake on fat release changed. Adipose PDE3B transcript levels decreased after fasting, with and without GH blockade. Model: Nine obese men; adipose biopsy after 72-hour fast. Limitations: Transcript level is not direct PDE3B enzyme activity. Evidence access: Primary full-text Results: Regulation of lipolysis, DOI 10.1210/jc.2016-3835 Substrate Metabolism and Insulin Sensitivity During Fasting in Obese Human Subjects: Impact of GH Blockade. · 2017 · https://pubmed.ncbi.nlm.nih.gov/28324055/ · DOI 10.1210/jc.2016-3835
    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